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Abstract
Neurology in Tropics (E-book)
Table of Contents
Section Title | Page | Action | Price |
---|---|---|---|
Cover | Cover | ||
Title Page | iii | ||
Copyright Page | iv | ||
Foreword | v | ||
Preface to the Second Edition | vii | ||
List of Contributors | ix | ||
Editorial Advisory Board | xvii | ||
Dedication | xix | ||
Contents | xxi | ||
Section I - CNS Infections | 1 | ||
Chapter 1 - HIV Infection in the Tropics | 3 | ||
Epidemiology | 3 | ||
Neuropathogenesis | 4 | ||
Clinical manifestations | 5 | ||
Intracranial Disorders | 5 | ||
HIV-Associated Neurocognitive Disorder (HAND) | 5 | ||
Clinical Features | 5 | ||
Neuromuscular Disorders | 5 | ||
Classification of Neuromuscular Disorders | 5 | ||
Distal Symmetric Polyneuropathy | 6 | ||
Clinical manifestations | 6 | ||
Mononeuropathy Multiplex | 6 | ||
Inflammatory Demyelinating Polyneuropathies | 7 | ||
Lumbosacral Polyradiculopathy | 7 | ||
Myopathy | 7 | ||
Clinical Manifestations | 7 | ||
Spinal Cord Disorders | 7 | ||
Sub-Acute Vacuolar Myelopathy | 7 | ||
Human T-Lymphotropic Virus-1–Associated Myelopathy | 7 | ||
Acute Myelopathies | 7 | ||
Intracranial Opportunistic Infections | 7 | ||
Toxoplasma Gondii | 7 | ||
Cryptococcus Neoformans | 8 | ||
Aseptic Meningitis | 8 | ||
Progressive Multifocal Leukoencephalopathy | 8 | ||
Viral Encephalitis | 8 | ||
Cytomegalovirus | 8 | ||
Neurosyphilis | 9 | ||
Neoplasms | 9 | ||
Central Nervous System Lymphoma | 9 | ||
Complications of systemic diseases | 9 | ||
Metabolic Encephalopathy | 9 | ||
Stroke | 9 | ||
Conclusion | 9 | ||
References | 9 | ||
Chapter 2 - HTLV-1 Infection in the Tropics | 11 | ||
Introduction | 11 | ||
Epidemiology | 11 | ||
Transmission | 12 | ||
HTLV-2 | 12 | ||
HTLV-3 and HTLV-4 | 12 | ||
Immunology and pathogenesis | 12 | ||
HAM/TSP | 13 | ||
Co-infection with HIV-1 and Hepatitis C | 14 | ||
Clinical characteristics | 14 | ||
HTLV-1 and Non-Neurological Disease | 14 | ||
Clinical Characteristics of HAM/TSP | 14 | ||
Other Neurological Complications Reported in Association with HTLV-1 Infection | 15 | ||
Diagnosis | 16 | ||
Laboratory Diagnosis | 16 | ||
Treatment | 16 | ||
Prognosis | 16 | ||
References | 17 | ||
Chapter 3 - Neurological Complications of Acute Haemorrhagic Conjunctivitis | 19 | ||
Introduction | 19 | ||
Epidemiology | 19 | ||
Predisposing Factors | 20 | ||
Aetiology | 20 | ||
Pathogenesis | 20 | ||
Clinical features | 21 | ||
Stage of Ophthalmic Infection | 21 | ||
Latent Stage | 22 | ||
Pre-paralytic/Prodromal Stage | 22 | ||
Paralytic Stage | 22 | ||
Spinal Cord Form | 22 | ||
Cranial Neuropathy Form | 22 | ||
Investigative abnormalities | 23 | ||
Cerebrospinal Fluid | 23 | ||
Virological Markers | 23 | ||
Neurophysiology | 23 | ||
HLA Studies | 24 | ||
Histological Studies | 24 | ||
Differential diagnosis | 24 | ||
Management | 24 | ||
Prognosis | 26 | ||
References | 26 | ||
Chapter 4 - Herpes Simplex Encephalitis | 28 | ||
Introduction | 28 | ||
Epidemiology | 28 | ||
Clinical features | 28 | ||
Pathology (by S.K. Shankar, NIMHANS, Bangalore) | 29 | ||
Investigations | 30 | ||
Cerebrospinal Fluid | 30 | ||
Magnetic Resonance Imaging (MRI) | 31 | ||
Electroencephalogram (EEG) | 31 | ||
Immunodiagnosis | 31 | ||
Brain Biopsy | 32 | ||
Differential diagnosis | 32 | ||
Treatment | 33 | ||
Prognosis | 33 | ||
Neonatal HSE | 33 | ||
HSE in AIDS | 34 | ||
References | 34 | ||
Chapter 5 - Japanese Encephalitis | 36 | ||
Introduction | 36 | ||
Epidemiology | 36 | ||
Human infection and pathogenesis | 37 | ||
Pathology (Professor Susarala K. Shankar, Nimhans, Bangalore, India) | 38 | ||
Clinical features | 40 | ||
Investigations | 40 | ||
Laboratory diagnosis | 41 | ||
Treatment and prevention | 42 | ||
References | 43 | ||
Chapter 6 - Dengue Fever: Neurological Complications | 45 | ||
Introduction | 45 | ||
Epidemiology | 45 | ||
Aetiology | 46 | ||
Pathogenesis | 46 | ||
Immunology and Molecular Biology | 46 | ||
Neuropathogenesis | 46 | ||
Neurotropism and Neurovirulence | 46 | ||
Post-Infectious Autoimmune Process | 47 | ||
Metabolic Disturbances and Haemorrhagic Complications | 47 | ||
Clinical characteristics | 47 | ||
Diagnosis | 48 | ||
Dengue Infection | 48 | ||
Cerebrospinal Fluid Analysis | 49 | ||
Diagnosis Imaging | 50 | ||
Pathology | 50 | ||
Differential diagnosis | 50 | ||
Treatment and prognosis | 50 | ||
References | 50 | ||
Chapter 7 - Nipah Encephalitis | 53 | ||
Introduction | 53 | ||
Epidemiology | 53 | ||
Why is IT not JE | 53 | ||
Nipah and hendra viruses: similar, yet different | 53 | ||
Bats as reservoir | 54 | ||
Outbreaks in Bangladesh and India | 54 | ||
Clinical manifestations | 54 | ||
Laboratory testing | 55 | ||
Radiological findings | 56 | ||
Histopathological findings | 57 | ||
Prognosis, relapses and late-onset nipah encephalitis | 57 | ||
Treatment | 58 | ||
Indications of future outbreak | 58 | ||
References | 59 | ||
Chapter 8 - Chikungunya – Neurological Complications | 60 | ||
Introduction | 60 | ||
Virology | 60 | ||
Epidemiology | 60 | ||
Pathogenesis | 61 | ||
Clinical features | 62 | ||
Severe and Atypical Forms | 63 | ||
Ocular Manifestations | 63 | ||
Neurological Complications | 63 | ||
Mother-to-Child Transmission | 64 | ||
Laboratory diagnosis | 65 | ||
Treatment | 65 | ||
Mortality and Morbidity | 65 | ||
Conclusions | 65 | ||
References | 65 | ||
Chapter 9 - Poliomyelitis | 68 | ||
Introduction | 68 | ||
Epidemiology | 68 | ||
Causative agent | 68 | ||
Pathogenesis | 68 | ||
Diagnosis | 68 | ||
Clinical features | 69 | ||
Treatment | 71 | ||
Poliovirus vaccines | 71 | ||
Post-polio syndrome (PPS) | 71 | ||
References | 72 | ||
Chapter 10 - Rabies | 73 | ||
Introduction | 73 | ||
Epidemiology | 73 | ||
Rabies in Asia | 73 | ||
Rabies in Europe | 74 | ||
Rabies in America | 74 | ||
Rabies in Africa | 74 | ||
Rabies in Australia | 74 | ||
Symptomless Carrier | 74 | ||
Infectious agent | 74 | ||
Pathogenesis and pathophysiology of rabies | 75 | ||
Mode of Transmission | 75 | ||
Uptake of Virus after Peripheral Inoculation | 75 | ||
Route of Centripetal Spread of Virus Uptake | 76 | ||
Replication of Virus in Inoculated Muscle | 77 | ||
Propagation of Virus Occurs only at Chemical Synapses | 77 | ||
Centrifugal Spread of Rabies Virus | 77 | ||
Neuronal Receptors for Rabies Virus | 77 | ||
Relevance of Neuropathogenesis to Incubation Period | 78 | ||
Furious Versus Paralytic Rabies: What is the Underlying Mechanism? | 78 | ||
Specific Viral Variants | 78 | ||
Extent of Immune Response | 78 | ||
Brainstem Inflammation | 78 | ||
Poor Immune Response in Rabies-Infected CNS | 78 | ||
Preservation of Neuronal Integrity | 79 | ||
Pathogenesis of Paralytic Rabies | 79 | ||
Pathology | 79 | ||
Clinical features | 80 | ||
Incubation Period | 80 | ||
Prodrome and Early Symptoms | 80 | ||
Acute Neurological Involvement | 81 | ||
Encephalitic Type | 81 | ||
Paralytic Rabies | 81 | ||
Coma | 82 | ||
Recovery | 82 | ||
Laboratory diagnosis of rabies | 82 | ||
Conventional Diagnostic Tests | 82 | ||
Direct Microscopy | 82 | ||
Demonstration of Viral Antigen | 82 | ||
Isolation of Virus | 83 | ||
Demonstration of Antibodies | 83 | ||
Newer Diagnostic Tests | 83 | ||
Demonstration of Viral Antigen | 83 | ||
Detection of Nucleic Acid | 84 | ||
Conclusions | 84 | ||
Demonstration of Antibodies | 84 | ||
Practical Application of Available Tests in Current Era | 84 | ||
Neuroimaging of Rabies | 84 | ||
Prevention of rabies | 85 | ||
History of Rabies Vaccines | 85 | ||
Post-Exposure Prophylaxis (PEP) | 86 | ||
Local Wound Care | 86 | ||
Estimation of Risk | 86 | ||
Different Types of Rabies Vaccines | 86 | ||
PEP for Previously Unvaccinated Patient | 87 | ||
PEP in Previously Vaccinated Patients | 88 | ||
PEP Failures | 89 | ||
Pre-Exposure Prophylaxis | 89 | ||
Management of rabies | 89 | ||
Therapy for Rabies | 89 | ||
New Approaches | 90 | ||
References | 90 | ||
Chapter 11 - Measles Pathobiology and Central Nervous System Complications | 93 | ||
Measles complications | 93 | ||
Pathogenesis | 94 | ||
Viral Entry into Brain | 95 | ||
PIE or ADEM | 95 | ||
Measles Inclusion Body Encephalitis (MIBE) | 95 | ||
Subacute sclerosing panencephalitis (SSPE) | 97 | ||
Epidemiology | 97 | ||
Pathogenesis | 98 | ||
Pathology | 99 | ||
Clinical features | 100 | ||
Long-term survivors | 101 | ||
Fulminant SSPE | 101 | ||
Diagnosis and treatment of SSPE | 101 | ||
CSF findings | 102 | ||
EEG | 103 | ||
Neuroimaging | 104 | ||
Treatment | 104 | ||
Prognosis | 104 | ||
Acknowledgements | 105 | ||
References | 105 | ||
Chapter 12 - Ebola Virus Disease | 109 | ||
Epidemiology | 109 | ||
Aetiology | 109 | ||
Transmission | 110 | ||
Immounology and pathogenesis | 110 | ||
Clinical characteristics | 110 | ||
Diagnosis and differential diagnosis | 111 | ||
Differential Diagnoses of EVD | 111 | ||
Treatment | 112 | ||
Prognosis | 112 | ||
References | 113 | ||
Chapter 13 - Leprosy | 114 | ||
Epidemiology | 114 | ||
Aetiology | 115 | ||
M. lepromatosis | 116 | ||
Pathogenesis of Leprosy | 116 | ||
Pathogenesis of Nerve Involvement in Leprosy | 116 | ||
Stages of Nerve Involvement | 117 | ||
Clinical features of leprosy | 118 | ||
Classification of leprosy | 118 | ||
Other Forms of Leprosy | 120 | ||
Neuropathy in leprosy | 121 | ||
Chronic Neuropathic Pain | 122 | ||
Diagnosis | 122 | ||
Differential Diagnosis | 122 | ||
Neurological Disorders | 122 | ||
Laboratory diagnosis | 122 | ||
Slit-Skin Smears | 123 | ||
Skin/Nerve Biopsy | 123 | ||
Immunohistochemistry | 123 | ||
Serology and PCR | 123 | ||
Reactions in Leprosy | 123 | ||
Type 1 Reaction | 123 | ||
Pathogenesis of Type 1 Reaction | 124 | ||
Type 2 Reaction | 124 | ||
Pathogenesis of Type 2 Reaction | 124 | ||
Systemic involvement | 124 | ||
Treatment | 125 | ||
Other regimens for special situations | 125 | ||
Immunotherapy | 125 | ||
Management of Lepra Reactions | 125 | ||
Treatment and Prophylaxis for Nerve Damage | 126 | ||
Prognosis | 126 | ||
References | 126 | ||
Chapter 14 - Leprosy in Africa | 128 | ||
Introduction | 128 | ||
Epidemiology | 128 | ||
Clinical features | 130 | ||
Tuberculoid Leprosy | 130 | ||
Lepromatous Leprosy | 130 | ||
Borderline Leprosy (Borderline Tuberculoid, Mid-Borderline and Borderline Lepromatous) | 131 | ||
Disabilities | 131 | ||
Diagnosis | 132 | ||
Treatment of leprosy | 132 | ||
Stigmatization | 133 | ||
Rehabilitation | 133 | ||
Prevention and Control | 133 | ||
References | 133 | ||
Chapter 15 - Pyogenic Meningitis | 134 | ||
Introduction | 134 | ||
Epidemiology | 134 | ||
Aetiology | 134 | ||
Neonatal | 135 | ||
Infancy and Childhood | 135 | ||
Adults | 135 | ||
Pre-Disposing Factors | 135 | ||
Pathogenesis | 136 | ||
Pathology (by Bishen D. Radotra Professor of Neuropathology, PGIMER, Chandigarh) | 136 | ||
Clinical features | 139 | ||
Investigations | 139 | ||
Differential diagnosis | 140 | ||
Management | 140 | ||
Empirical Antibiotic Therapy | 140 | ||
Meningococcal Meningitis | 142 | ||
Fulminant Meningococcemia | 143 | ||
H. influenzae Meningitis | 143 | ||
Antibiotic Therapy | 143 | ||
Seizures | 143 | ||
Pneumococcal Meningitis | 143 | ||
Alternative Antibiotics | 144 | ||
Streptococcal and Staphylococcal Meningitis | 144 | ||
Gram-Negative Bacillary Meningitis33 | 144 | ||
Listeria Meningitis | 144 | ||
Neonatal Meningitis | 144 | ||
Role of Corticosteroids | 145 | ||
Raised Intracranial Pressure | 145 | ||
Non-Antibiotic Aspects of Therapy | 145 | ||
Circulatory and Electrolyte Changes | 145 | ||
Partially Treated Pyogenic Meningitis37 | 145 | ||
Recurrent Bacterial Meningitis38,39 | 145 | ||
Prophylaxis | 146 | ||
Prognosis | 146 | ||
References | 146 | ||
Chapter 16 - Neurobrucellosis | 148 | ||
Introduction | 148 | ||
Epidemiology | 148 | ||
Aetiology | 148 | ||
Immunology and pathogenesis | 149 | ||
Clinical characteristics | 149 | ||
Clinical Features of Brucellosis | 149 | ||
Common Neurological Clinical Features | 149 | ||
Rare Neurological Clinical Features | 150 | ||
Diagnosis and differential diagnosis | 150 | ||
Treatment | 152 | ||
Prognosis | 152 | ||
References | 152 | ||
Chapter 17 - Neuroleptospirosis | 155 | ||
Introduction | 155 | ||
History | 155 | ||
Aetiological agents | 155 | ||
Epidemiology | 156 | ||
Transmission of infection | 156 | ||
High-risk groups | 156 | ||
Pathogenesis | 156 | ||
Clinical manifestations | 157 | ||
Neurological manifestations | 158 | ||
Leptospiral Meningitis | 159 | ||
Encephalitis and Encephalomyelitis | 159 | ||
Transverse Myelitis | 159 | ||
Intracranial Haemorrhage | 159 | ||
Ocular Manifestations | 159 | ||
Peripheral Nerves | 159 | ||
Other Neurological Manifestations | 159 | ||
Investigations | 160 | ||
Differential diagnosis | 161 | ||
Treatment | 161 | ||
Prognosis | 161 | ||
Prevention | 161 | ||
Summary | 161 | ||
References | 162 | ||
Chapter 18 - Neurological Manifestations of Syphilis | 164 | ||
History and epidemiology | 164 | ||
Overview of neurosyphilis | 164 | ||
Early manifestations of syphilis | 165 | ||
Introduction | 165 | ||
Case Report 1 | 165 | ||
Case Report 2 | 166 | ||
Case Report 3 | 166 | ||
Case Report 4 | 167 | ||
Asymptomatic Neurosyphilis and Early Meningeal Syphilis | 167 | ||
Case Report 5 | 167 | ||
Case Report 6 | 168 | ||
Meningovascular syphilis | 168 | ||
Late neurosyphilis | 170 | ||
General Paresis of the Insane (Dementia Paralytica) | 170 | ||
Tabes Dorsalis (or Locomotor Ataxia) | 171 | ||
Other Spinal Manifestations | 171 | ||
Other Ophthalmological Problems | 172 | ||
Syphilitic Osteitis and Gummas | 172 | ||
HIV and syphilis | 172 | ||
Congenital syphilis | 173 | ||
Early Manifestations | 173 | ||
Late Manifestations | 174 | ||
Diagnosis | 174 | ||
Interpretation of Serological Testing for Syphilis | 174 | ||
False-Positive Syphilis Serology Tests | 174 | ||
Future Tests | 175 | ||
Treatment | 175 | ||
Recommended Treatment Regimens | 175 | ||
Key messages | 175 | ||
References | 176 | ||
Chapter 19 - Neurological Manifestation of Enteric Fever | 177 | ||
Introduction | 177 | ||
Epidemiology | 177 | ||
Transmission and Risk Factors | 177 | ||
Global Burden of Disease | 177 | ||
Asia and the Indian Subcontinent | 177 | ||
Pathogenesis | 179 | ||
Clinical manifestation | 179 | ||
Neurological Complications of Enteric Fever | 179 | ||
Typhoid Delirium | 179 | ||
Meningitis | 180 | ||
Specific Neurological Syndromes | 180 | ||
Focal Cortical Dysfunction | 180 | ||
Cerebellar Ataxia | 181 | ||
Psychiatric Disorder | 181 | ||
Myelopathy | 181 | ||
Peripheral Neuropathy | 181 | ||
Extrapyramidal Syndrome | 181 | ||
Outcome | 182 | ||
Conclusions | 182 | ||
References | 182 | ||
Chapter 20 - Tuberculous Meningitis | 183 | ||
Section A: Introduction and Epidemiology | 183 | ||
Introduction | 183 | ||
Epidemiology | 183 | ||
Section B: Pathophysiology and Pathology | 184 | ||
Pathophysiology | 184 | ||
Pathology | 185 | ||
Section C: Clinical Features and Diagnosis | 188 | ||
Clinical features | 188 | ||
Diagnosis | 189 | ||
Microscopy | 189 | ||
Bacteriology | 190 | ||
CSF examination and other diagnostic aids | 191 | ||
Section D: Role of Imaging | 192 | ||
Imaging features | 192 | ||
CT | 192 | ||
MRI | 193 | ||
Differential diagnosis | 194 | ||
Imaging of Complications | 194 | ||
Clinical algorithms | 195 | ||
Treatment | 196 | ||
Antituberculosis Treatment | 196 | ||
Adjunctive Immunomodulatory Treatment | 198 | ||
Antiretroviral Therapy | 198 | ||
Managing hyponatrAemia | 199 | ||
Section E: Role of Surgery in TBM | 199 | ||
Managing hydrocephalus | 199 | ||
Management | 199 | ||
Surgical Management | 199 | ||
Role of endoscopy | 200 | ||
Endoscopic Third Ventriculostomy | 200 | ||
Septum Pellucidotomy | 201 | ||
Adhesiolysis | 201 | ||
Prognostic factors and outcome | 201 | ||
Prevention – vaccination | 202 | ||
Summary | 202 | ||
References | 202 | ||
Chapter 21 - CNS Tuberculomas | 206 | ||
Section A: Epidemiology and Clinical Features | 206 | ||
Introduction | 206 | ||
Epidemiology | 206 | ||
Section B: Pathology of Tuberculomas | 207 | ||
Pathogenesis | 207 | ||
Pathology | 208 | ||
Clinical features | 209 | ||
Appearance of New Lesion and Paradoxical Expansion of Intracranial Tuberculomas During Chemotherapy | 210 | ||
Diagnosis | 211 | ||
Section C: Brain Imaging | 211 | ||
CT | 211 | ||
MRI | 212 | ||
Role of Advanced Imaging | 214 | ||
Section D: Surgery in Tuberculomas | 214 | ||
Indications for surgery | 215 | ||
To Obtain a Definitive Diagnosis | 215 | ||
Stereotactic Biopsy | 216 | ||
Stereotactic Craniotomy | 217 | ||
Microsurgery | 217 | ||
Intracranial Pressure | 217 | ||
Tissue for Culture and Sensitivity Studies | 217 | ||
Tuberculomas with Intractable Epilepsy | 217 | ||
Complications of surgery | 217 | ||
Microbiological studies | 218 | ||
Section E: Medical Management | 218 | ||
Antitubercular therapy | 218 | ||
Role of steroids | 219 | ||
Prognosis | 219 | ||
References | 219 | ||
Chapter 22 - Amoebic Infections of Central Nervous System | 222 | ||
Introduction | 222 | ||
Acanthamoeba | 222 | ||
Epidemiology and Life Cycle | 222 | ||
Human Infections | 224 | ||
Granulomatous amoebic encephalitis | 224 | ||
Epidemiology | 224 | ||
Pathogenesis and Pathology | 224 | ||
Clinical Features | 224 | ||
Laboratory Diagnosis | 224 | ||
Neuroimaging | 224 | ||
Microscopic Methods | 225 | ||
Culture Methods | 225 | ||
Serology | 225 | ||
PCR | 225 | ||
Management | 226 | ||
B. mandrillaris | 226 | ||
Epidemiology and Life Cycle | 226 | ||
Human Infections | 226 | ||
Balamuthia amoebic meningitis | 226 | ||
Epidemiology, Pathogenesis and Pathology | 226 | ||
Clinical Features | 227 | ||
Laboratory Diagnosis | 227 | ||
Neuroimaging | 227 | ||
Microscopic Method | 227 | ||
Culture Methods | 227 | ||
Serology | 228 | ||
PCR | 228 | ||
Treatment | 228 | ||
N. fowleri | 229 | ||
Epidemiology and Life Cycle | 229 | ||
Primary amoebic meningoencephalitis | 230 | ||
Epidemiology | 230 | ||
Pathogenesis and Pathology | 230 | ||
Clinical Features | 230 | ||
Laboratory Diagnosis | 230 | ||
Light Microscopy | 230 | ||
CSF | 230 | ||
Brain tissue | 230 | ||
Neuroimaging | 230 | ||
Culture methods | 230 | ||
PCR | 230 | ||
Management | 230 | ||
Conclusions | 231 | ||
References | 231 | ||
Chapter 23 - Neurological Complications of Malaria | 233 | ||
Introduction | 233 | ||
Epidemiology | 233 | ||
Biology | 233 | ||
Clinical features | 234 | ||
Cerebral Malaria | 234 | ||
Definition | 234 | ||
Clinical Presentation | 234 | ||
Pathogenesis | 236 | ||
Brain Pathology (by Bishen D. Radotra, Professor of Neuropathology, PGIMER, Chandigarh) | 237 | ||
Diagnosis and assessment | 238 | ||
Neuroimaging | 238 | ||
Management | 239 | ||
Adjunctive Therapy | 239 | ||
Malaria Vaccine | 240 | ||
Future research | 240 | ||
References | 240 | ||
Chapter 24 - Human African Trypanosomiasis | 241 | ||
Introduction | 241 | ||
Epidemiology | 241 | ||
History | 241 | ||
Parasites | 242 | ||
Vectors | 242 | ||
Reservoirs | 242 | ||
Geographical Repartition | 243 | ||
Immunology and pathogenesis | 243 | ||
General Features | 243 | ||
Pathological Manifestations in the CNS | 244 | ||
Clinical characteristics | 244 | ||
Lymphaticosanguine Stage or Stage 1 | 245 | ||
Meningoencephalitic Stage or Stage 2 | 245 | ||
Clinical Forms | 246 | ||
Diagnosis | 246 | ||
Diagnosis of HAT (Screening) | 247 | ||
Diagnosis of Stage (Staging) | 247 | ||
Treatment | 247 | ||
Treatment of Stage 1 | 248 | ||
Treatment of Stage 2 | 248 | ||
Post-Treatment Follow-Up | 248 | ||
References | 248 | ||
Chapter 25 - Neurocysticercosis | 251 | ||
Introduction | 251 | ||
Life cycle of T. solium | 251 | ||
Evolutionary stages of cysticercus | 252 | ||
Clinical presentations | 253 | ||
Classification and Diagnostic Criteria | 254 | ||
Seizures and Epilepsy | 255 | ||
Meningeal–Subarachnoid NCC | 256 | ||
Heavy Multilesional Parenchymal Cysticerci | 256 | ||
Cysticercotic encephalitis | 256 | ||
Heavy non-encephalitic NCC | 256 | ||
Disseminated cysticercosis | 256 | ||
Intraventricular NCC | 258 | ||
Solitary Cysticercus Granuloma | 258 | ||
Uncommon Manifestations | 260 | ||
Serological diagnosis of NCC | 260 | ||
Radiology and imaging | 260 | ||
Treatment of NCC | 260 | ||
Anticysticercal Agents | 260 | ||
Corticosteroids | 261 | ||
Antiepileptic Drugs | 261 | ||
Overview of Treatment Decisions | 262 | ||
Treatment of SCG | 262 | ||
References | 262 | ||
Chapter 26 - Hydatid Disease of the Central Nervous System | 264 | ||
Introduction | 264 | ||
Aetiopathogenesis | 264 | ||
E. granulosus Infection | 265 | ||
Structure of the Intracranial E. granulosus Hydatid Cyst | 265 | ||
E. multilocularis Infection | 266 | ||
Intracranial hydatid cysts | 266 | ||
Clinical Presentation | 267 | ||
Radiological Diagnosis | 267 | ||
Skull X-Ray | 267 | ||
CT | 267 | ||
Magnetic Resonance Imaging | 267 | ||
Magnetic Resonance Spectroscopy | 268 | ||
Serological Diagnosis | 268 | ||
Differential Diagnosis | 269 | ||
Treatment | 269 | ||
Surgical Considerations | 271 | ||
Pitfalls in Management and their Avoidance | 271 | ||
Complications | 271 | ||
Medical Treatment | 273 | ||
Prognosis | 273 | ||
Prophylaxis | 273 | ||
Spinal and vertebral hydatid cysts | 273 | ||
Clinical Presentation | 274 | ||
Radiological Diagnosis | 274 | ||
Treatment | 274 | ||
Extradural Lesions | 274 | ||
Intradural Lesions | 276 | ||
Calvarial and intracranial epidural hydatid disease | 276 | ||
Orbital hydatid cyst | 276 | ||
Acknowledgements | 277 | ||
References | 277 | ||
Chapter 27 - Neurofilariasis | 279 | ||
Introduction | 279 | ||
Epidemiology | 280 | ||
Global Scenario | 281 | ||
Indian Scenario | 281 | ||
Aetiology | 281 | ||
Immunology and pathogenesis | 282 | ||
Host–Parasite Interaction and Mode of Invasion | 283 | ||
Immunobiology and Typical Immune Signalling | 283 | ||
Molecular biology | 284 | ||
Clinical characteristics | 284 | ||
Diagnosis and differential diagnosis of NF | 284 | ||
Direct Visualization Using Microscopic Technique | 284 | ||
Microscopic Detection of mf | 285 | ||
Electroclinical Techniques | 285 | ||
Neuroimaging (Especially MRI, electroencephalography (EEG)) | 285 | ||
Cerebrospinal Fluid Analysis | 285 | ||
Immunodiagnosis | 286 | ||
Serodiagnosis | 286 | ||
Antigen Test | 286 | ||
Mazzotti or Patch Test (Inflammation After DEC Administration) | 286 | ||
Antibody Test | 286 | ||
Western Blotting and Immunoprecipitation | 286 | ||
Histopathology | 286 | ||
Molecular diagnosis | 286 | ||
PCR | 286 | ||
Differential Diagnosis of NF | 287 | ||
Metabolomics-Based Diagnosis | 287 | ||
Treatment | 287 | ||
Anthelmintics | 287 | ||
Antibiotics | 288 | ||
Vaccines | 288 | ||
Prognosis | 288 | ||
Concluding remarks and future perspectives | 289 | ||
References | 289 | ||
Chapter 28 - Neuroangiostrongylosis | 291 | ||
Introduction | 291 | ||
Epidemiology | 291 | ||
Aetiology | 292 | ||
Agent | 292 | ||
Incubation Period | 292 | ||
Immunology and pathogenesis | 292 | ||
Life Cycle of A. cantonensis | 292 | ||
Hosts of A. cantonensis | 293 | ||
Intermediate Hosts | 293 | ||
Paratenic Hosts | 293 | ||
Definite Hosts | 293 | ||
Accidental Hosts (Infection of Humans) | 293 | ||
Immunological Aspects | 295 | ||
Molecular biology | 295 | ||
Clinical characteristics | 295 | ||
Eosinophilic Meningitis/Encephalitis | 295 | ||
Adults | 295 | ||
Children | 295 | ||
Ocular Angiostrongylosis | 296 | ||
Diagnosis and differential diagnosis | 296 | ||
Probable Diagnosis | 297 | ||
Definite Diagnosis | 297 | ||
Neuropathology | 297 | ||
Treatment | 298 | ||
Prevention | 298 | ||
Medication | 298 | ||
Applicable to Humans | 298 | ||
Experimental | 298 | ||
Prognosis | 298 | ||
References | 298 | ||
Chapter 29 - Neuroschistosomiasis | 301 | ||
Introduction | 301 | ||
Epidemiology | 301 | ||
Aetiology | 301 | ||
Immunology and Pathogenesis | 302 | ||
Molecular Biology | 304 | ||
Clinical characteristics | 304 | ||
Diagnosis and differential diagnosis | 306 | ||
Routine laboratory diagnosis | 306 | ||
Treatment | 306 | ||
Prognosis | 307 | ||
References | 307 | ||
Chapter 30 - Neurognathostomiasis | 309 | ||
Introduction | 309 | ||
Epidemiology | 309 | ||
Aetiology | 309 | ||
Pathogenesis | 310 | ||
Immunity | 311 | ||
Clinical features | 311 | ||
Diagnosis | 312 | ||
Differential diagnosis | 313 | ||
Treatment | 313 | ||
Prognosis | 313 | ||
References | 313 | ||
Chapter 31 - Onchocerciasis and its Potential Association with Epilepsy | 315 | ||
Introduction | 315 | ||
Prevalence of Onchocerciasis | 315 | ||
Life Cycle of O. volvulus | 315 | ||
Clinical Manifestations of Onchocerciasis | 315 | ||
Onchocerciasis and Epilepsy: Epidemiology | 318 | ||
Onchocerciasis and Nodding Syndrome: Epidemiology, Clinical Description and Classification | 318 | ||
Onchocerciasis and Epilepsy/Nodding Syndrome: Suggested Pathomechanisms | 319 | ||
Diagnosis of Onchocerciasis | 321 | ||
Treatment of Onchocerciasis and its Potentially Associated Epilepsy/Nodding Syndrome | 322 | ||
Acknowledgement | 323 | ||
References | 323 | ||
Chapter 32 - Fungal Infections of Central Nervous System in Tropics | 327 | ||
Introduction | 327 | ||
Epidemiology | 327 | ||
Pathogenesis | 327 | ||
Clinical syndromes | 328 | ||
Meningitis | 328 | ||
Focal Mass Lesions | 328 | ||
Rhinocerebral Syndromes | 328 | ||
Stroke Syndromes | 328 | ||
Spinal Syndromes | 328 | ||
CNS fungal infections common in tropical countries | 328 | ||
Cryptococcal Meningitis | 328 | ||
CNS aspergillosis | 330 | ||
Mucormycosis | 331 | ||
Other Rare CNS Fungal Infections in Tropical Countries | 332 | ||
References | 334 | ||
Section II - Nutritional disordersand neurotoxicology | 337 | ||
Chapter 33 - Malnutrition and Nervous System in Children | 339 | ||
Introduction | 339 | ||
Epidemiology | 339 | ||
Nature and evolution of malnutrition | 339 | ||
Scenario in South Asia | 341 | ||
Nutritional deficiency | 343 | ||
Classification | 343 | ||
Protein energy malnutrition | 343 | ||
Malnutrition and nervous system | 345 | ||
Malnutrition and Brain Development | 345 | ||
Clinical features | 346 | ||
Radiology | 346 | ||
Electroencephalographic Findings | 347 | ||
Evoked Potentials | 347 | ||
Visual-Evoked Potentials | 347 | ||
Brainstem Auditory-Evoked Potentials (BAEP) | 348 | ||
Somatosensory-Evoked Potentials | 348 | ||
Motor-Evoked Potential | 348 | ||
Endogenous Event-Related Potentials | 348 | ||
Malnutrition and PNS | 348 | ||
Nerve Conduction Studies and Electromyography | 348 | ||
Malnutrition and Autonomic Nervous System | 348 | ||
Micronutrient deficiencies associated with malnutrition | 349 | ||
Management of malnutrition | 349 | ||
Prevention | 349 | ||
Dietary Management of Malnutrition | 350 | ||
Conclusions | 350 | ||
References | 351 | ||
Chapter 34 - Nutrition Rehabilitation of Children with Protein Energy Malnutrition (PEM) in Developing Countries | 353 | ||
Introduction | 353 | ||
Epidemiology | 353 | ||
Aetiology | 353 | ||
Classification of Protein Energy Malnutrition | 355 | ||
Diagnosis of PEM | 355 | ||
Moderate Malnutrition | 356 | ||
Severe Malnutrition | 356 | ||
Management of PEM | 357 | ||
Assessment of Children with PEM | 357 | ||
Weight for Height | 358 | ||
Height for Age | 358 | ||
Weight for Age | 358 | ||
Practical Guidelines for Management of Children with SAM in India at the Community/Family Based Level | 360 | ||
Prevention of PEM | 360 | ||
Key Messages | 361 | ||
References | 361 | ||
Chapter 35 - Infantile Tremor Syndrome | 362 | ||
Introduction | 362 | ||
Epidemiology | 362 | ||
Aetiopathogenesis | 363 | ||
Clinical features | 364 | ||
Mental and Physical Retardation or Regression | 364 | ||
Tremor | 364 | ||
Hair Changes | 364 | ||
Skin Pigmentation | 364 | ||
Pallor | 364 | ||
Other Features | 364 | ||
Course of the Disease | 365 | ||
Investigations | 365 | ||
Haematologic | 365 | ||
Radiology | 366 | ||
Neuro-Radiology | 366 | ||
Virological Studies | 366 | ||
Electroencephalography (EEG) | 366 | ||
Brain Biopsy | 366 | ||
Liver Biopsy | 366 | ||
Rectal Biopsy | 366 | ||
Muscle Biopsy | 366 | ||
Trace Element Study | 366 | ||
Differential diagnosis | 366 | ||
Treatment | 366 | ||
Prognosis | 367 | ||
Future Trends | 367 | ||
References | 367 | ||
Chapter 36 - Lathyrism | 369 | ||
Introduction | 369 | ||
History and epidemiology | 369 | ||
Aetiology | 371 | ||
Lathyrus sativus L. | 371 | ||
Lathyrus Toxins | 372 | ||
Pathogenesis | 372 | ||
Nuero Pathology | 372 | ||
Clinical and electrophysiological features | 373 | ||
Clinical Presentation of Lathyrism | 373 | ||
Associated Disorders | 374 | ||
Diagnosis | 374 | ||
Prognosis | 375 | ||
Prevention and treatment | 375 | ||
Regulatory Aspects | 375 | ||
Treatment | 375 | ||
Prevention | 375 | ||
Utilization | 376 | ||
Conclusions | 376 | ||
References | 376 | ||
Chapter 37 - Konzo: A Permanent, Non-Progressive Motor Neuron Disorder | 379 | ||
Introduction | 379 | ||
Epidemiology | 379 | ||
Aetiology | 381 | ||
Clinical characteristics | 383 | ||
Diagnosis | 385 | ||
Differential Diagnosis | 385 | ||
Treatment, prognosis and prevention | 385 | ||
References | 386 | ||
Chapter 38 - Tropical Ataxic Neuropathy | 389 | ||
Introduction | 389 | ||
Historical aspects | 389 | ||
Nosology | 390 | ||
Epidemiology | 390 | ||
Clinical features | 391 | ||
Demographic Characteristics | 391 | ||
Neurological Symptoms and Signs | 391 | ||
Laboratory Findings | 393 | ||
Diagnosis and Differential Diagnosis | 394 | ||
Aetiopathogenesis | 394 | ||
Treatment | 395 | ||
Conclusions | 395 | ||
References | 395 | ||
Chapter 39 - Minamata Disease | 397 | ||
Introduction | 397 | ||
Epidemiology | 397 | ||
Pathology | 398 | ||
Clinical features | 398 | ||
Diagnosis | 399 | ||
Congenital or fOetal minamata disease | 399 | ||
Treatment | 400 | ||
References | 400 | ||
Chapter 40 - Neurotoxins in Tropics/India: An Overview | 401 | ||
Introduction | 401 | ||
Classification | 402 | ||
Non-Biological | 403 | ||
Others | 404 | ||
Insects | 406 | ||
Reptiles | 408 | ||
Amphibians | 408 | ||
Marine and Aquatic Creatures | 409 | ||
Microorganisms (Bacteria) | 410 | ||
Non-Biological Neurotoxins | 410 | ||
Lead | 411 | ||
Mercury | 411 | ||
Manganese | 412 | ||
Arsenic | 412 | ||
Cadmium | 413 | ||
Tin | 413 | ||
Gold | 413 | ||
Man-Made Neurotoxic Chemicals | 413 | ||
Pesticides | 415 | ||
Organic Solvents | 416 | ||
Gases | 418 | ||
Plastics and Polymers | 419 | ||
Food Additives Beverages | 419 | ||
Contaminated Drinking Water in Pune | 420 | ||
Cosmetics and Related Products | 420 | ||
Waste from Electrics and Electronics Equipment (WEEE) | 421 | ||
Mobile Towers and Cell Phone | 422 | ||
Acknowledgements | 424 | ||
References | 424 | ||
Chapter 41 - Marine Neurotoxins | 428 | ||
Introduction | 428 | ||
Food chain toxins | 428 | ||
Ciguatera | 428 | ||
Ciguatoxin (CTX), Maitotoxin (MTX) and Scaritoxin (SCTX) | 428 | ||
Palytoxin (PTX) | 430 | ||
Domoic Acid (DA) | 430 | ||
Saxitoxin (STX) | 431 | ||
Neurotoxic (Non-Paralytic) Shellfish Poisoning (NSP) | 431 | ||
Tetrodotoxin (TTX) | 431 | ||
Cyanobacterial Neurotoxins | 433 | ||
Envenomations and Contact Toxins | 434 | ||
Venomous Fish Toxins | 434 | ||
Stingray Toxins | 435 | ||
Scorpionfish Toxins | 436 | ||
Weeverfish Toxins | 437 | ||
Catfish Toxins | 437 | ||
Sea-Snake Toxins | 437 | ||
Conotoxins | 439 | ||
Octopus Toxins | 440 | ||
Coelenterate Toxins | 441 | ||
Echinotoxins | 443 | ||
Environmental Interactions | 444 | ||
References | 444 | ||
Chapter 42 - Fluorosis | 448 | ||
Introduction | 448 | ||
Epidemiology | 450 | ||
Recent Clinical and Experimental Observations on the Effect of Fluoride on Bones | 450 | ||
Role of Strontium and Other Trace Elements in the Incidence of Skeletal Fluorosis in Endemic Areas of Fluorosis in Prakasam... | 451 | ||
Clinical features | 451 | ||
Dental Fluorosis | 451 | ||
Pre-Skeletal Stage | 452 | ||
Skeletal Fluorosis | 452 | ||
Endemic Genu Valgum | 453 | ||
Neurological Manifestations of Skeletal Fluorosis | 453 | ||
Myelopathy | 453 | ||
Radiculopathy | 453 | ||
Cranial Nerve Lesions | 454 | ||
Peripheral Neuropathies | 454 | ||
Cerebrovascular Accidents | 454 | ||
Laboratory investigations | 454 | ||
Electrophysiological Studies | 454 | ||
Pulmonary Function Tests | 455 | ||
Scintigraphic Studies | 456 | ||
Radiology of Fluorosis | 456 | ||
Computed Tomography | 458 | ||
Magnetic Resonance Imaging | 459 | ||
Pathology | 460 | ||
Histopathology of Bones | 461 | ||
Muscle and Nerve Pathology | 461 | ||
Muscle Pathology | 461 | ||
Conclusion of Muscle and Nerve Studies | 466 | ||
Differential Diagnosis | 466 | ||
Treatment | 468 | ||
Optimum water fluoride concentration | 468 | ||
Prevention of Endemic Skeletal Fluorosis | 468 | ||
Medical Therapy | 469 | ||
Surgical Management of Skeletal Fluorosis with Neurological Manifestations | 469 | ||
Conclusions | 471 | ||
References | 471 | ||
Chapter 43 - Organophosphorous Poisoning | 473 | ||
Introduction | 473 | ||
History | 473 | ||
Epidemiology | 473 | ||
Pathophysiology | 474 | ||
Clinical features | 475 | ||
Laboratory manifestations | 476 | ||
Clinical Neurophysiology | 476 | ||
Treatment | 479 | ||
Decontamination | 480 | ||
Pharmocological therapy | 480 | ||
References | 482 | ||
Chapter 44 - Snake Bites | 483 | ||
Introduction | 483 | ||
Prevention of Snake Bites | 483 | ||
Epidemiology | 484 | ||
Africa | 484 | ||
Asia | 484 | ||
Oceania | 484 | ||
Americas | 484 | ||
Europe | 485 | ||
Snake Bite as an Occupational Disease | 487 | ||
Aetiology | 487 | ||
Venomous Snakes: Numbers of Species | 487 | ||
Classification | 487 | ||
Distinguishing Snakes from Other Snake-Like Animals | 488 | ||
Distinguishing Venomous from Non-Venomous Snakes | 488 | ||
Venom Apparatus | 489 | ||
Distribution of Venomous Snakes | 489 | ||
Venomous Snake Bite Without Envenoming (Dry Bites) | 490 | ||
Immunology and pathogenesis | 491 | ||
Venom Composition | 491 | ||
Venom Enzymes | 491 | ||
Cardiovascular Toxins | 491 | ||
Neurotoxins | 491 | ||
Pathogenesis of the Clinical Effects of Envenoming | 492 | ||
Local Swelling | 492 | ||
Hypotension and Shock | 492 | ||
Anti-Haemostatic Disturbances | 492 | ||
Intravascular Haemolysis | 492 | ||
Acute Kidney Injury (AKI) | 492 | ||
Neurotoxicity | 493 | ||
Descending Flaccid Paralysis | 493 | ||
Autonomic Nervous System Effects | 493 | ||
Drowsiness | 493 | ||
Myotoxicity | 493 | ||
Clinical characteristics | 493 | ||
Envenoming by Different Groups of Venomous Snakes | 493 | ||
Colubrid (Back-fanged Snakes), Families Colubridae and Dipsadidae | 493 | ||
Atractaspidinae (Burrowing Asps or Stiletto Snakes and Natal Black Snake) | 494 | ||
Elapidae (Cobras, Kraits, Mambas, Coral Snakes, Sea Snakes) | 494 | ||
Local Envenoming | 494 | ||
Systemic Envenoming | 495 | ||
Neurotoxic Effects | 495 | ||
Other Features of Systemic Envenoming | 495 | ||
Viperidae (Old World Vipers and Adders, New World Pit Vipers, Rattlesnakes, Moccasins and Lance-Headed Vipers, Asian Pit Vi... | 497 | ||
Local Envenoming | 497 | ||
Antihaemostatic Abnormalities | 497 | ||
Intravascular Haemolysis | 500 | ||
Hypotension and Shock | 500 | ||
Acute Kidney Injury | 500 | ||
Neurotoxicity and Generalized Rhabdomyolysis | 500 | ||
Diagonsis and differential diagnosis | 501 | ||
Immunodiagnosis and PCR | 501 | ||
Laboratory Investigations Blood Count | 502 | ||
Twenty-Minute Whole Blood Clotting Test (20WBC) | 502 | ||
Serum Biochemistry | 502 | ||
Electrocardiography | 502 | ||
Radiology and Imaging | 502 | ||
Histopathology | 504 | ||
Treatment | 504 | ||
First Aid | 504 | ||
Recommendations | 505 | ||
Methods for Delaying the Onset of Potentially Fatal Systemic Envenoming | 505 | ||
Pressure-Immobilization Methods | 505 | ||
Inhibition of the Lymphatic Pump | 505 | ||
Dangerous and Rejected First-Aid Methods | 505 | ||
Pre-Hospital Treatment of Early Symptoms | 505 | ||
Hospital Treatment | 506 | ||
Clinical Assessment | 506 | ||
Antivenom | 506 | ||
Indications | 507 | ||
Cautions | 507 | ||
Prediction of Antivenom Reactions | 507 | ||
Prevention of Antivenom Reactions | 507 | ||
Specific and Para-Specific Neutralization by Antivenoms | 507 | ||
Shelf-Life of Antivenoms | 507 | ||
How Soon to Start Antivenom Treatment | 507 | ||
Antivenom Administration | 507 | ||
Dosage | 508 | ||
Recurrent Envenoming | 508 | ||
Indications for Second and Subsequent Doses | 508 | ||
Antivenom Reactions | 508 | ||
Treatment for Failing Systems and Organs | 508 | ||
Respiratory Failure | 508 | ||
Circulatory Failure | 509 | ||
Renal Failure (AKI) | 509 | ||
Treatment of Other Complications | 509 | ||
Wound Infection | 509 | ||
Intracompartmental Syndrome and Fasciotomy | 509 | ||
Dangerous and Unproven Treatments | 510 | ||
Snake Venom Ophthalmia | 510 | ||
Clinical course and prognosis | 510 | ||
Risk of Death from Envenoming | 510 | ||
Interval Between Bite and Death | 510 | ||
References | 510 | ||
Chapter 45 - Tetanus | 514 | ||
Introduction | 514 | ||
Historical aspect | 514 | ||
C. tetani and Its Toxin: Chemistry, Biological Action, Transport and Pathogenesis | 514 | ||
Epidemiology | 515 | ||
Clinical feature | 516 | ||
Severity of tetanus | 517 | ||
Diagnosis | 517 | ||
Electromyographic studies | 517 | ||
Differential diagnosis | 517 | ||
Neonatal tetanus (NT) | 518 | ||
Management | 519 | ||
Supportive Intensive Care | 519 | ||
Control of Rigidly and Spasm | 519 | ||
Control of Autonomic Dysfunction | 519 | ||
Neutralizing Circulating Toxin | 520 | ||
Removal of Source of Tetanospasmin | 520 | ||
Prevention | 520 | ||
Complications | 520 | ||
Prognosis and sequel | 520 | ||
Conclusions | 521 | ||
References | 521 | ||
Section III - Neuromuscular diseases | 523 | ||
Chapter 46 - Tropical Neuropathies | 525 | ||
Introduction | 525 | ||
Nutritional neuropathies | 525 | ||
Protein Calorie Malnutrition (PCM) | 525 | ||
Clinical, Electrophysiological and Histological Derangements | 526 | ||
Histology | 526 | ||
Vitamin Deficiency | 526 | ||
Thiamine (B1) | 527 | ||
Niacin | 528 | ||
Vitamin B6 (Pyridoxine) | 528 | ||
Vitamin B12 (Cobalamine) | 529 | ||
Epidemic neuropathy in Cuba (1992–3) | 529 | ||
Tropical sprue | 530 | ||
Tropical myeloneuropathies | 531 | ||
Tropical Ataxic Neuropathy (TAN) | 532 | ||
Tropical Spastic Paraparesis (TSP) | 533 | ||
Acute/Epidemic Spastic Paraparesis | 534 | ||
Lathyrism | 534 | ||
Konzo | 534 | ||
Infections and post-infectiuous neuropathies | 535 | ||
Directly Infectious Syndromes | 535 | ||
Leprosy | 535 | ||
Rabies | 536 | ||
Enterovirus 70 (EV70) | 536 | ||
HIV Infection | 537 | ||
Parasites | 538 | ||
Infectious Toxin-Mediated Syndromes | 538 | ||
Diphtheric Neuropathy | 538 | ||
Tetanus | 539 | ||
Post-infective polyneuropathy | 539 | ||
Acute Motor Axonal Neuropathy (AMAN) or Chinese Paralytic Syndrome | 539 | ||
Toxic neuropathies | 540 | ||
Clinical features | 540 | ||
Aetiology of Toxic Neuropathies | 541 | ||
Heavy Metals | 541 | ||
Arsenic | 541 | ||
Lead | 542 | ||
Drugs | 543 | ||
Post-Vaccinal Encephaloneuropathies | 544 | ||
Insecticides | 545 | ||
Industrial Chemicals | 546 | ||
Methyl-iso-cyanide (MIC) | 547 | ||
Plant and Animal Toxins | 547 | ||
Animal Poisons | 548 | ||
Neuropathies due to physical injury | 548 | ||
Entrapment and traumatic neruopathies | 548 | ||
Conclusions | 549 | ||
References | 549 | ||
Chapter 47 - Motor Neuron Disease in Tropics | 553 | ||
Introduction | 553 | ||
Environment and MND | 553 | ||
Diagnostic Criteria for ALS | 553 | ||
Classification | 554 | ||
Aetiopathogenesis | 555 | ||
Pathology | 555 | ||
Intracellular Inclusions | 556 | ||
Aetiology | 556 | ||
SOD1-Mediated Toxicity | 557 | ||
Inflammatory Responses | 557 | ||
Excitotoxicity | 557 | ||
Abnormalities of RNA Metabolism | 557 | ||
Cytoskeletal Derangements | 557 | ||
Mitochondrial Dysfunction | 557 | ||
Viral Infections | 557 | ||
Apoptosis | 557 | ||
Growth Factors | 557 | ||
Clinical features | 558 | ||
Differential diagnosis | 558 | ||
Investigations | 559 | ||
Treatment | 559 | ||
Symptom-based management | 560 | ||
Respiratory Management | 560 | ||
Dysarthria | 560 | ||
Dysphagia | 560 | ||
Disease-modifying treatment of ALS | 561 | ||
Mechanism of Action | 561 | ||
Other Drugs Tried | 561 | ||
Current and Future Trials | 561 | ||
Gene Therapy | 561 | ||
Monomelic variants of MND | 561 | ||
Hirayama disease | 563 | ||
Wasted leg syndrome | 563 | ||
MND in Western India | 563 | ||
MND in South India | 563 | ||
Conclusions | 564 | ||
References | 564 | ||
Chapter 48 - Motor Neuron Disease in Africa | 566 | ||
Introduction | 566 | ||
Epidemiology | 566 | ||
Aetiology and risk factors | 567 | ||
Molecular pathogenesis | 567 | ||
Pathology | 568 | ||
Clinical characteristics | 568 | ||
Diagnosis | 569 | ||
Differential Diagnoses of MND | 569 | ||
Treatment | 569 | ||
Prognosis | 571 | ||
References | 571 | ||
Chapter 49 - Tropical Pyomyositis | 573 | ||
Introduction | 573 | ||
Epidemiology | 573 | ||
Aetiopathogenesis | 574 | ||
Microbiology | 574 | ||
Role of Trauma | 574 | ||
Anatomical Distribution | 575 | ||
Predisposing Factors | 575 | ||
Age and Sex | 575 | ||
Malnutrition | 575 | ||
Parasitic and Viral Myositis | 575 | ||
Immune Deficiency | 575 | ||
Pyomyositis and HIV Infection | 575 | ||
Medical Diseases | 576 | ||
Pathological features | 576 | ||
Clinical characteristics | 576 | ||
Clinical Types of Pyogenic Myositis | 577 | ||
Tropical and Non-Tropical Pyomyositis | 577 | ||
Psoas Abscess | 577 | ||
Piriformis Pyomyositis | 577 | ||
Diagnosis and differential diagnosis | 577 | ||
Investigations | 577 | ||
Routine Laboratory Parameters | 577 | ||
Imaging Studies | 578 | ||
Needle Aspiration | 579 | ||
Treatment | 579 | ||
Initial Choice of Antibiotics | 579 | ||
Immunocompetent Patients | 579 | ||
Immunocompromized Patients | 580 | ||
Duration of Therapy and Follow-Up | 580 | ||
Prognosis | 580 | ||
Conclusions | 580 | ||
References | 580 | ||
Section IV - Cerebrovascular diseases | 583 | ||
Chapter 50 - Epidemiology of Stroke in Tropics | 585 | ||
Introduction | 585 | ||
Stroke in Latin American countries | 585 | ||
Prevalence and Incidence | 585 | ||
Risk Factors of Stroke in Latin America | 585 | ||
Stroke from Asian countries: Association of South-East Asian Nations | 586 | ||
Singapore | 586 | ||
Other Asian Countries | 586 | ||
South Asia | 586 | ||
Indian Scenario | 586 | ||
Prevalence | 586 | ||
Incidence Rates | 587 | ||
Case-Fatality Rates (CFR) | 587 | ||
Mean Age of Stroke | 587 | ||
Risk Factors | 587 | ||
Subtypes of Stroke | 588 | ||
Long-term sequel of stroke survivors | 589 | ||
Stroke Awareness | 589 | ||
Stroke in countries other than India | 589 | ||
Stroke in Africa | 590 | ||
Stroke in Australia, New Zealand and French West Indies | 590 | ||
Disease Burden | 591 | ||
References | 591 | ||
Chapter 51 - Transient Ischaemic Attack (TIA): Recent Concepts | 594 | ||
Epidemiology | 594 | ||
Definition of transient ischaemic attack | 594 | ||
Stroke risk after TIA | 595 | ||
TIA mimics | 596 | ||
Management | 596 | ||
Lifestyle Modifications | 597 | ||
Antiplatelet Therapy | 597 | ||
Anticoagulation Therapy | 597 | ||
Antihypertensive Therapy | 597 | ||
Statins | 597 | ||
Control of Diabetes Mellitus | 598 | ||
Carotid Endarterectomy | 598 | ||
Conclusions | 598 | ||
References | 598 | ||
Chapter 52 - Current Concepts of Ischaemic Stroke | 600 | ||
Introduction | 600 | ||
Pathology | 600 | ||
Subacute and Chronic Infarcts with Glial Scar | 602 | ||
Lacunar Infarcts and Multi-Infarct Dementia | 602 | ||
Arterial Vasospasm and Delayed Cerebral Ischaemia | 602 | ||
Pathobiology of Ischaemic Lesions of the Brain | 603 | ||
Stroke imaging | 606 | ||
Imaging in Hyperacute Ischaemic Stroke | 606 | ||
CT Scan | 606 | ||
MRI | 607 | ||
Imaging in Ischaemic Stroke – Beyond the Hyperacute Stage | 609 | ||
Diagnosis and management | 609 | ||
Triage and Initial Evaluation | 610 | ||
History | 611 | ||
Physical Examination | 611 | ||
Neurological Examination | 611 | ||
Hyperacute Thrombolysis with Recombinant Tissue Plasminogen Activator | 612 | ||
Other New Interventions | 613 | ||
Aspirin | 613 | ||
General Treatment Recommendations | 613 | ||
Brain Oedema and Increased Intracranial Pressure | 614 | ||
Management in a Stroke Unit | 614 | ||
Stroke Outcome | 614 | ||
Stroke Mortality and Disability | 615 | ||
Stroke Recurrence | 615 | ||
Thrombolysis in Tropical Countries | 615 | ||
Asia | 615 | ||
Africa | 615 | ||
Latin America | 616 | ||
Australasia | 616 | ||
Acknowledgements | 616 | ||
References | 616 | ||
Chapter 53 - Uncommon Causes of Ischaemic Stroke | 618 | ||
Introduction | 618 | ||
Moyamoya disease | 618 | ||
Clinical Features | 618 | ||
Other Symptoms | 618 | ||
Diagnosis | 619 | ||
Medical Management | 619 | ||
Surgery | 620 | ||
Treatment of Acute Symptoms | 620 | ||
Prognosis | 620 | ||
Takayasu arteritis | 620 | ||
Clinical Features | 620 | ||
Diagnosis | 620 | ||
Non-Invasive Imaging | 621 | ||
Treatment | 621 | ||
Medical Management | 621 | ||
Surgical Treatment | 621 | ||
Follow-Up | 621 | ||
Arterial dissection | 621 | ||
Stroke Mechanisms of Dissection | 622 | ||
Clinical Manifestations | 622 | ||
Diagnosis | 623 | ||
Treatment | 623 | ||
Fibromuscular dysplasia | 623 | ||
Pathology | 624 | ||
Diagnosis | 624 | ||
Management | 624 | ||
Infections and stroke | 624 | ||
Tuberculosis | 624 | ||
Diagnosis of TBM | 626 | ||
Imaging | 626 | ||
Management | 626 | ||
Bacterial Infections | 626 | ||
Fungal Infections | 626 | ||
Parasitic Infections | 627 | ||
Viral Infections | 627 | ||
Varicella Zoster Virus Vasculopathy | 627 | ||
HIV | 628 | ||
CADASIL | 628 | ||
Hypercoagulable states | 629 | ||
References | 630 | ||
Chapter 54 - Secondary Prevention of Transient Ischaemic Attack and Ischaemic Stroke | 633 | ||
Introduction | 633 | ||
Events in ischaemic brain injury | 633 | ||
Symptoms of ischaemic brain injury (TIA/early stroke) | 633 | ||
Risk factors | 634 | ||
Differential Diagnosis | 634 | ||
Key Points on Guidelines | 635 | ||
Therapeutic considerations in stroke prevention | 636 | ||
Secondary Prevention Strategies of Ischaemic Stroke (TIA and Early Infarct) | 636 | ||
Antiplatelet Agents in Prevention of Non-Cardioembolic Stroke/TIA | 636 | ||
Aspirin | 636 | ||
Aspirin and Dipyridamole | 637 | ||
Aspirin Plus Clopidogrel | 638 | ||
Thienopyridine | 638 | ||
Antiplatelet Agents for Secondary Prevention of Stroke | 638 | ||
Key Points | 638 | ||
Anticoagulation Therapy in Cerebral Ischaemia | 638 | ||
Trials with New/Novel Oral Anticoagulants | 638 | ||
Cardioembolic Strokes – Anticoagulation in Prevention | 639 | ||
Non-Cardioembolic Stroke – Anticoagulation Therapy | 639 | ||
Concluding remarks | 640 | ||
Antithrombotic Agents in Cerebral Ischaemia | 640 | ||
Raised Homocysteine (tHcy) Level –‘An Independent Risk Factor’ for Vascular Disease | 640 | ||
Statins and Stroke – Current Views | 640 | ||
Recommendations | 640 | ||
Stenting and Angioplasty in Symptomatic Carotid Stenosis | 640 | ||
Summary/recommendations | 641 | ||
Acknowledgements | 641 | ||
References | 641 | ||
Chapter 55 - Intracerebral Haemorrhage | 644 | ||
Introduction and epidemiology | 644 | ||
Aetiology | 644 | ||
Pathophysiology and cascade of brain damage | 644 | ||
Clinical features | 644 | ||
Management of ICH | 646 | ||
Emergency Department and In-Hospital Care | 646 | ||
Laboratory Investigations | 646 | ||
Monitoring | 646 | ||
Immediate Management | 647 | ||
Neuroimaging | 647 | ||
Haematoma Size Estimation | 647 | ||
Predicting Haematoma Expansion and the Spot Sign | 648 | ||
Prognostic ICH Scoring System | 650 | ||
Treatment | 650 | ||
Raised Intracranial Pressure | 650 | ||
Oral Anticoagulant–Associated ICH | 651 | ||
Heparin-Induced ICH | 653 | ||
Post-Thrombolytic ICH | 653 | ||
Glucose Monitoring | 653 | ||
Seizure | 653 | ||
BP Management | 654 | ||
Evidences Towards Lowering BP in ICH | 654 | ||
Surgical Management of ICH | 655 | ||
To Do Surgical Intervention or Not and Which Patient? Major Craniotomy Trials | 655 | ||
Minimally Invasive Surgical Removal | 656 | ||
Timing of Surgery | 657 | ||
Intraventricular Haemorrhage | 658 | ||
Non-Neurological Complications of ICH | 660 | ||
GI Haemorrhage | 660 | ||
Temperature | 660 | ||
Prognosis | 660 | ||
End-of-Care Issues | 661 | ||
Rehabilitation and Recovery | 661 | ||
ICH future therapies | 661 | ||
References | 661 | ||
Chapter 56 - Cerebral Venous Sinus Thrombosis | 665 | ||
Introduction | 665 | ||
Epidemiology of CVT in Asia | 665 | ||
Aetiology | 666 | ||
Genetic Causes of CVT | 666 | ||
Factor V | 666 | ||
Factor V Leiden | 666 | ||
Factor V A4070G | 666 | ||
Prothrombin | 667 | ||
Factor XII | 667 | ||
Protein Z | 667 | ||
Plasminogen Activator Inhibitor-1 | 667 | ||
Tissue Factor Pathway Inhibitor 1 | 667 | ||
Methylene Tetrahydrofolate Reductase | 668 | ||
Janus Kinase-2 | 668 | ||
Factor VIII | 668 | ||
Protein C, Protein S and Antithrombin | 668 | ||
Clinical features and presentation | 668 | ||
Syndrome of Raised Intracranial Hypertension without Focal Deficit | 669 | ||
Syndrome of Focal Motor Deficit with or without Raised Intracranial Hypertension | 669 | ||
Syndrome of Early Altered Consciousness with Involuntary Movements | 669 | ||
Syndrome of Cavernous Sinus Thrombosis | 669 | ||
Pathology | 669 | ||
Gross Pathology | 670 | ||
Histology | 671 | ||
Pathogenesis | 672 | ||
Investigation and diagnosis | 673 | ||
MRI and Angiography | 673 | ||
Management | 675 | ||
Chemical and Mechanical Thrombolysis | 676 | ||
Decompressive Craniectomy | 676 | ||
Outcome | 677 | ||
References | 678 | ||
Chapter 57 - Stroke Unit in the Tropics | 680 | ||
Introduction | 680 | ||
Rising Burden of Stroke in Tropics | 680 | ||
Why Stroke Unit Care? | 680 | ||
What is a stroke unit? | 681 | ||
Key Components of a Stroke Unit | 681 | ||
Inside a Stroke Unit | 681 | ||
Development (history) of stroke units | 683 | ||
What are the different types of stroke units? | 683 | ||
Efficacy of stroke unit care in developed nations | 683 | ||
Applicability of Stroke Units in Low-/Middle-Income Countries | 683 | ||
Challenges of stroke unit care delivery (barriers to implementation) in low-/middle-income countries | 686 | ||
Lessons learnt – summary | 687 | ||
Areas where further studies are needed | 687 | ||
Hope for tomorrow | 688 | ||
References | 688 | ||
Chapter 58 - Stroke in the Young | 689 | ||
Introduction | 689 | ||
Epidemiology | 689 | ||
Vascular risk factors in young adult stroke | 689 | ||
Smoking | 690 | ||
Alcohol Consumption | 690 | ||
Oral Contraceptives | 690 | ||
Illicit Drugs | 690 | ||
Migraine | 690 | ||
Differential diagnosis | 690 | ||
Aetiology | 690 | ||
Diagnosis of Cardioembolism | 691 | ||
Diagnosis of Extracranial or Intracranial Large Vessel Arterial Disease | 691 | ||
Diagnosis of Small Vessel Disease | 692 | ||
Diagnosis of Other Identifiable Causes | 692 | ||
Infections | 692 | ||
Arterial Dissection | 692 | ||
Primary and Secondary Vasculitis and Connective Tissue Disorders | 693 | ||
Other Rare Non-Inflammatory Arteriopathies | 693 | ||
Monogenic Diseases | 693 | ||
Pregnancy and Puerperium | 693 | ||
Undetermined Cause or Cryptogenic Stroke | 693 | ||
Treatment | 694 | ||
Acute Treatment | 694 | ||
Secondary Prevention | 694 | ||
Prognosis | 694 | ||
Stroke in the young: Indian perspective | 695 | ||
Risk Factors | 695 | ||
References | 696 | ||
Section V - Epilepsy | 699 | ||
Chapter 59 - Epilepsy in the Tropics | 701 | ||
Introduction | 701 | ||
Epidemiology | 701 | ||
Aetiology | 703 | ||
Pathogenesis | 703 | ||
Clinical Characteristics, Diagnosis and Differential Diagnosis | 704 | ||
Pharmacological treatment | 705 | ||
The Treatment Gap and Social Aspects | 705 | ||
Surgical Treatment | 705 | ||
Prognosis | 706 | ||
References | 706 | ||
Chapter 60 - Central Nervous System Infections and Epilepsy | 707 | ||
Introduction | 707 | ||
Burden of epilepsy with CNS infections | 707 | ||
Pathophysiological considerations | 708 | ||
Anatomical Compartmentalization of the Infection | 708 | ||
CNS infections | 709 | ||
Bacterial Meningitis | 709 | ||
Viral Encephalitis | 709 | ||
Malaria | 709 | ||
Neurocysticercosis | 710 | ||
Uncommon CNS Infections | 710 | ||
Association between CNS infections and epilepsy | 713 | ||
Prevalence Studies | 713 | ||
Incidence Studies | 714 | ||
Therapeutic considerations in relation to CNS infections, seizures and epilepsy | 714 | ||
Optimal Choice of Antiepileptic Drugs in the Treatment of Epilepsy Associated with CNS Infections | 715 | ||
References | 716 | ||
Chapter 61 - Hot Water Epilepsy | 718 | ||
Introduction | 718 | ||
Epidemiology | 718 | ||
Clinical features | 718 | ||
Pathogenesis | 720 | ||
Genetics | 720 | ||
Electroencephalography (EEG) findings | 723 | ||
Autonomic changes | 724 | ||
SPECT observations | 724 | ||
fMRI study and network alterations | 724 | ||
Management | 724 | ||
Conclusions | 725 | ||
Acknowledgement | 725 | ||
References | 725 | ||
Chapter 62 - Reflex Seizures and Reflex Epilepsies in Tropical Countries | 727 | ||
Introduction | 727 | ||
Definition | 728 | ||
Classification | 729 | ||
Pathophysiology | 730 | ||
More frequently encountered reflex epilepsy syndromes in tropics | 730 | ||
Hot Water Epilepsy | 730 | ||
Epidemiology | 730 | ||
Clinical Features | 731 | ||
EEG Characteristics | 731 | ||
Pathophysiology | 733 | ||
Eating Epilepsy | 733 | ||
Startle Epilepsy | 734 | ||
Prevalence of Photosensitivity in Tropics | 734 | ||
Conclusions | 735 | ||
References | 735 | ||
Chapter 63 - Surgery for Epilepsy in Tropical Countries | 737 | ||
Introduction | 737 | ||
Challenges in establishing epilepsy surgery programs in tropics | 737 | ||
Identification of Potential Surgical Candidates | 738 | ||
Pre-Surgical Evaluation | 738 | ||
Present state of epilepsy surgery in tropical countries | 742 | ||
Epilepsy Surgery in Tropical Asia | 742 | ||
Epilepsy Surgery in Tropical Latin America | 742 | ||
Epilepsy Surgery in Tropical Africa | 744 | ||
Regionally Prevalent Lesional Epilepsy Syndromes | 744 | ||
Surgical Treatment Gap | 745 | ||
Temporal Trends in Epilepsy Surgery | 745 | ||
Epilepsy Surgery Outcome | 745 | ||
Is Epilepsy Surgery Cost-Effective? | 746 | ||
Pragmatic Epilepsy Surgery Models for Tropical Regions | 746 | ||
Conclusions | 748 | ||
References | 749 | ||
Section VI - Demyelinationand degeneration | 751 | ||
Chapter 64 - Multiple Sclerosis in Tropics | 753 | ||
Introduction | 753 | ||
Epidemiology | 753 | ||
Aetiology | 753 | ||
MS and Genes | 753 | ||
MS and the Environment | 754 | ||
EB Virus and MS | 754 | ||
Vitamin D Intake and MS | 755 | ||
Cigarette Smoking | 756 | ||
Pathology | 756 | ||
Clinical characteristics | 756 | ||
Diagnosis | 757 | ||
Differential Diagnosis of MS | 757 | ||
Treatment | 758 | ||
Disease-Modifying Therapies (DMT) | 759 | ||
Interferon Beta (IFN-beta) | 759 | ||
Glatiramer Acetate | 759 | ||
Natalizumab | 760 | ||
Oral Drugs | 760 | ||
Fingolimod | 760 | ||
Teriflunomide | 760 | ||
Dimethyl Fumarate | 760 | ||
Mitoxantrone | 760 | ||
Oral Immunosuppressant Agents | 760 | ||
Symptomatic Therapy | 761 | ||
Statins in MS | 761 | ||
References | 761 | ||
Chapter 65 - Neuromyelitis Optica Spectrum Disorders | 764 | ||
Introduction | 764 | ||
Original Concepts, Evolution of Diagnosis and Diagnostic Criteria | 764 | ||
Epidemiology | 764 | ||
Aetiology | 765 | ||
Clinical features | 765 | ||
Extra-Optico Spinal Manifestations of NMO | 766 | ||
Co-existing autoimmune disease and autoantibodies | 766 | ||
Clinical course and outcome | 766 | ||
Paediatric NMO | 766 | ||
Pathogenesis | 767 | ||
Pathology | 767 | ||
Histopathology | 767 | ||
Immunopathology | 767 | ||
Diagnosis | 767 | ||
Imaging of NMO | 767 | ||
Anti-Aquaporin Antibodies | 769 | ||
Cerebrospinal Fluid | 769 | ||
Differential Diagnosis | 770 | ||
Treatment | 770 | ||
Management of Acute Attacks | 770 | ||
Intravenous Steroids | 770 | ||
Plasma Exchange | 770 | ||
Attack Prevention | 770 | ||
General Principles | 770 | ||
Other Immunosuppressants | 771 | ||
Prognosis | 771 | ||
Acknowledgements | 772 | ||
References | 772 | ||
Chapter 66 - Post-Infectious and Post-Vaccine Acute Disseminated Encephalomyelitis | 775 | ||
Introduction | 775 | ||
Epidemiology | 775 | ||
Aetiology | 775 | ||
Viral Aetiologies | 775 | ||
Bacterial Aetiologies | 777 | ||
Non-Microbial Aetiologies | 777 | ||
Post-Vaccinal Acute Disseminated Encephalomyelitis | 777 | ||
Pathogenesis | 778 | ||
Clinical features | 778 | ||
Diagnosis | 779 | ||
Laboratory Diagnosis | 779 | ||
Cerebrospinal Fluid | 779 | ||
Electroencephalography | 779 | ||
Neuroimaging | 779 | ||
Brain Biopsy | 780 | ||
Differential diagnosis | 781 | ||
Treatment | 782 | ||
Prognosis | 783 | ||
References | 783 | ||
Chapter 67 - Neurological Manifestations of Behçet Disease | 788 | ||
Introduction | 788 | ||
Epidemiology | 788 | ||
Neuropathology | 789 | ||
Pathogenesis | 789 | ||
Clinical manifestations | 790 | ||
Parenchymal or Intra-Axial NBD | 790 | ||
Brainstem Syndrome | 790 | ||
Psychiatric and Cognitive Disorders | 790 | ||
Headache | 791 | ||
Epilepsy | 791 | ||
Isolated Spinal Cord Involvement | 791 | ||
Other rare manifestations | 791 | ||
Acute Meningeal Syndrome | 791 | ||
Movement Disorders | 791 | ||
Peripheral Nervous System Involvement | 791 | ||
Optic Neuropathy | 791 | ||
Subclinical Neuro-Behçet Syndrome | 791 | ||
Non-Parenchymal NBD | 792 | ||
Cerebral Venous Thrombosis | 792 | ||
Arterial Neuro-Behçet Syndrome | 792 | ||
Diagnosis of NBD | 792 | ||
Neuroimaging | 792 | ||
Cerebrospinal Fluid | 793 | ||
Other Diagnostic Methods | 794 | ||
Neurophysiological Tests | 794 | ||
Differential diagnosis | 794 | ||
Prognosis | 795 | ||
Management | 795 | ||
Treatment of Parenchymal NBD | 795 | ||
Treatment of Non-Parenchymal NBD | 795 | ||
References | 796 | ||
Chapter 68 - Dementia in Tropics | 798 | ||
Introduction | 798 | ||
Epidemiology | 798 | ||
Prevalence of Dementia: India | 798 | ||
Incidence of Dementia in India | 798 | ||
Causes of dementia | 799 | ||
Reversible dementias | 799 | ||
Clinical features | 799 | ||
Alzheimer Disease | 799 | ||
Frontotemporal lobar degeneration | 801 | ||
Frontotemporal Dementia | 801 | ||
Semantic Dementia | 802 | ||
Progressive Non-Fluent Aphasia (PNFA) | 802 | ||
Mixed Dementia (MD) | 802 | ||
Dementia with Lewy Bodies (DLBD) | 802 | ||
Vascular Dementia (VAD) | 802 | ||
Creutzfeldt–Jakob Disease | 803 | ||
Genetic factors in dementias | 803 | ||
Genetic Factors in AD | 803 | ||
Genetics Factors in FTLD | 804 | ||
Genetic Forms of Vascular Dementia | 804 | ||
Neuroimaging of dementias | 804 | ||
CT and MRI | 804 | ||
Magnetic Resonance Spectroscopy (MRS) | 804 | ||
Functional Activation Using MRI | 805 | ||
Functional Imaging | 805 | ||
Management of Dementia | 807 | ||
Pharmacological treatment | 807 | ||
Cholinesterase Inhibitors (ChEIs) | 807 | ||
Cholinesterase Inhibitors in Severe Alzheimer Disease | 808 | ||
Memantine in Alzheimer Disease | 808 | ||
Vascular Dementia | 808 | ||
Dementia with Lewy Bodies (DLBD) and Parkinson Disease Dementia | 808 | ||
Conclusions | 809 | ||
References | 809 | ||
Chapter 69 - Vascular Dementia | 812 | ||
Introduction | 812 | ||
Disease burden associated with vascular dementia | 812 | ||
Risk factors for vascular dementia | 813 | ||
Stroke and Vascular Dementia | 813 | ||
Vascular Risk Factors and Dementia | 814 | ||
Genetics and Vascular Dementia | 814 | ||
Subtypes of Vascular Dementia | 814 | ||
Large-Vessel Dementia or Multi-Infarct Dementia | 814 | ||
Small-Vessel Dementia or Subcortical Vascular Dementia | 815 | ||
Strategic Infarct Dementia | 815 | ||
Pathology and pathogenesis of vascular dementia | 815 | ||
Relation of vascular dementia with alzheimer’s disease | 816 | ||
Uncommon Causes of Vascular Dementia | 816 | ||
Diagnosis of vascular dementia | 816 | ||
Diagnostic Criteria for Vascular Dementia | 816 | ||
Clinical Assessment of Vascular Dementia | 819 | ||
Neuropsychology of Vascular Dementia | 819 | ||
Multi-Infarct Dementia | 820 | ||
Subcortical Vascular Dementia | 820 | ||
Strategic Infarct Dementia | 820 | ||
Behaviour in Vascular Dementia | 821 | ||
Investigations for Vascular Dementia | 822 | ||
Treatment of vascular dementia | 824 | ||
Prognosis for vascular dementia | 825 | ||
Conclusions | 825 | ||
References | 825 | ||
Chapter 70 - Rapidly Progressive Dementia | 830 | ||
Introduction | 830 | ||
Definition | 830 | ||
Epidemiology | 830 | ||
Aetiology | 830 | ||
Clinical characteristics | 831 | ||
Creutzfeldt–Jakob Disease (CJD) | 832 | ||
Degenerative Diseases | 833 | ||
Infections | 834 | ||
Bacterial Infections | 834 | ||
Neurosyphilis | 834 | ||
Tuberculosis | 835 | ||
Whipple Disease | 835 | ||
Viral infections | 835 | ||
Human Immunodeficiency Virus (HIV) | 835 | ||
Fungal infection | 836 | ||
Parasitic infections | 836 | ||
Neurocysticercosis | 836 | ||
Vascular Causes | 837 | ||
Autoimmune Disorders | 837 | ||
Hashimoto’ Encephalopathy | 837 | ||
Neurosarcoidosis | 838 | ||
Behcet Disease | 838 | ||
Metabolic Causes | 838 | ||
Normal Pressure Hydrocephalus | 838 | ||
Psychiatric Causes | 838 | ||
Neoplastic | 838 | ||
Diagnosis and differential diagnosis | 838 | ||
Clinical Assessment | 838 | ||
Laboratory Testing | 839 | ||
Electroencephalography | 840 | ||
Cerebrospinal Fluid | 840 | ||
Neuroimaging | 840 | ||
Brain Biopsy | 840 | ||
Differential diagnosis | 840 | ||
Treatment | 841 | ||
Prognosis | 841 | ||
Acknowledgement | 841 | ||
References | 841 | ||
Chapter 71 - Dementia in Africa | 844 | ||
Introduction | 844 | ||
Epidemiology | 844 | ||
Prevalence of Dementia in Africa | 844 | ||
Prevalent Dementia Subtypes | 846 | ||
Incidence of Dementia in Africa | 846 | ||
Analytic Studies of Dementia | 847 | ||
Aetiology | 847 | ||
Clinical characteristics | 848 | ||
Diagnosis and differential diagnosis | 848 | ||
Treatment | 848 | ||
Prognosis | 848 | ||
Conclusions | 849 | ||
References | 849 | ||
Chapter 72 - Hereditary Ataxia in the Tropical World | 850 | ||
Introduction | 850 | ||
Spinocerebellar ataxia | 850 | ||
SCA 1 | 850 | ||
SCA 2 | 851 | ||
SCA 3 | 851 | ||
SCA 6 | 852 | ||
SCA 12 | 852 | ||
Autosomal dominant episodic ataxia | 853 | ||
Friedreich ataxia | 853 | ||
Ataxia telangiectasia | 853 | ||
Ataxia with vitamin E deficiency | 853 | ||
Acknowledgements | 854 | ||
References | 854 | ||
Section VII - Miscellaneous | 857 | ||
Chapter 73 - History of Tropical Neurology | 859 | ||
Introduction | 859 | ||
Nutritional disorders and tropical neurology | 861 | ||
Notable features of some neurological disorders in India | 863 | ||
Degenerative and Demyelinating Disorders | 863 | ||
Congenital disorders | 866 | ||
The epilepsies | 866 | ||
Peripheral neuropathies | 867 | ||
Tuberculosis and other infections | 867 | ||
Study of tropical neurology in Africa and South America | 869 | ||
History of neurology in India | 870 | ||
References | 877 | ||
Chapter 74 - Neuroepidemiology for Planning of the Health Structure of the Country | 881 | ||
Introduction | 881 | ||
Common uses of epidemiology in general | 881 | ||
Role of Epidemiologist | 881 | ||
Epidemiological Framework for the Delivery of Health Care Services | 881 | ||
Epidemiological Transition | 882 | ||
Causation Framework | 882 | ||
Social Determinants of Health | 882 | ||
Environmental Challenges | 882 | ||
Challenges in neuroepidemiological researches | 882 | ||
Delivery of Neurological Services in Developing Countries | 883 | ||
Prevention | 884 | ||
Primary Prevention | 884 | ||
Secondary Prevention | 885 | ||
Tertiary Prevention | 885 | ||
References | 885 | ||
Chapter 75 - Headache Peculiarities in the Tropics | 887 | ||
Introduction | 887 | ||
Epidemiology | 888 | ||
Epidemiology of Headache in Africa | 888 | ||
Epidemiology of Headache in India | 890 | ||
Ophthalmoplegic Migraine | 890 | ||
Treatment | 892 | ||
Factors Influencing Headache Care in Tropics | 892 | ||
Management of Headache in Tropics | 893 | ||
Disability Impacts of Headaches | 894 | ||
Conclusions | 894 | ||
References | 894 | ||
Chapter 76 - Heat Stroke | 896 | ||
Introduction | 896 | ||
Epidemiology | 896 | ||
Aetiology | 897 | ||
Clothing and Equipment | 897 | ||
Environment | 898 | ||
Wet Bulb Globe Temperature | 898 | ||
Work Facilities | 898 | ||
Peer or Organizational Pressure | 898 | ||
Lack of Medical Personnel | 898 | ||
Dehydration | 898 | ||
Inappropriate Work-to-Rest Ratio | 898 | ||
History of Heat Stroke | 898 | ||
Predisposing Medical Condition, Illnesses and Fever | 898 | ||
Age | 899 | ||
Personality | 899 | ||
Poor Physical Fitness and Body Composition | 899 | ||
Lack of Heat Acclimatization | 899 | ||
Delayed Recognition of Warning Signs | 900 | ||
Sleep Loss | 900 | ||
Supplements | 900 | ||
Pathogenesis | 900 | ||
Normal Response to Heat Stress | 900 | ||
Thermoregulatory Failure Leading to Heat Stroke | 900 | ||
Influence of Hydration | 901 | ||
Clinical characteristics | 902 | ||
Recognition and diagnosis | 902 | ||
Treatment | 902 | ||
On-Site Treatment | 902 | ||
In-Hospital Treatment | 904 | ||
Vital Sign Assessment and Initial Management | 904 | ||
Cooling | 904 | ||
Haemodynamic Management | 904 | ||
Complications and Treatments | 905 | ||
Prognostic Indicators | 905 | ||
Emerging Treatment Options | 906 | ||
Prognosis | 906 | ||
Return to Participation and Work Considerations | 906 | ||
Recommendations for Heat Stroke Recovery | 906 | ||
Heat Tolerance Testing | 907 | ||
References | 907 | ||
Chapter 77 - Movement Disorders in Tropics | 909 | ||
Introduction | 909 | ||
Parkinson disease and parkinsonism | 909 | ||
Epidemiology | 909 | ||
Indian Scenario | 909 | ||
X-linked dystonia parkinsonism (Lubag syndrome) | 910 | ||
Toxin-induced parkinsonism (manganese-induced) | 910 | ||
Infectious causes of parkinsonism | 910 | ||
Common Infections | 910 | ||
Viral Infections | 910 | ||
Parasitic Infections | 910 | ||
Prion Disease | 910 | ||
Bacterial Causes | 910 | ||
Bacterial Infection | 910 | ||
Tubercular Meningitis | 910 | ||
Viral Infections | 911 | ||
SSPE | 911 | ||
Japanese B Encephalitis | 911 | ||
HIV and AIDS | 911 | ||
Parasitic Infections | 912 | ||
Malaria | 912 | ||
Neurocysticercosis | 912 | ||
Prion Diseases | 912 | ||
CJD and Other Prion Diseases | 912 | ||
Dystonia | 912 | ||
Wilson Disease | 912 | ||
Chorea | 912 | ||
Sydenham Chorea | 912 | ||
AIDS | 913 | ||
Wilson Disease | 914 | ||
Tremor | 914 | ||
Infantile Tremor Syndrome | 914 | ||
SCA12 | 914 | ||
Myoclonus | 914 | ||
Myoclonus in SSPE | 914 | ||
Myoclonus in Wilson Disease | 915 | ||
Tics | 915 | ||
References | 915 | ||
Chapter 78 - Future Developments in Tropical Neurology | 918 | ||
Introduction | 918 | ||
Disease pattern of neurological diseases in tropics | 918 | ||
Infective and Communicable Diseases Affecting Nervous System | 918 | ||
Non-Communicable Diseases Affecting Nervous System | 919 | ||
Development in diagnosis | 919 | ||
Future developments in treatment of tropical diseases | 920 | ||
Scope of Rehabilitation | 921 | ||
Prevention of tropical diseases | 921 | ||
Communicable Diseases | 921 | ||
Non-Communicable Disease | 921 | ||
Neurogenetics | 921 | ||
Improvement of Social Determinants of Health | 921 | ||
Conclusions | 922 | ||
Acknowledgement | 922 | ||
References | 922 | ||
Chapter 79 - Climate Change: What Neurologists Should Know | 923 | ||
Introduction | 923 | ||
The climate | 923 | ||
What Are Climate Change and Global Warming? | 923 | ||
Has Climate Change Begun? | 924 | ||
What About Regional Climate Change Effects? | 924 | ||
How Does the Climate System Work? | 924 | ||
What Is the Greenhouse Effect? | 924 | ||
What Are Greenhouse Gases? | 924 | ||
What Are the Causes of the Global Warming? | 925 | ||
Why Is Fossil Fuel Combustion Such an Important Factor? | 925 | ||
Environmental neurology | 925 | ||
Overview | 925 | ||
What Are the Neurological Outcomes of Climate Change? | 925 | ||
Stroke Impacted by Air Pollution and Climate Change | 926 | ||
CNS Infections: Encephalitis and Meningitis | 927 | ||
Hypertension and Salinity of Drinking Water | 928 | ||
Nervous System Responses to Toxic Factors | 928 | ||
Fungi and Mycotoxins | 928 | ||
Seafood Poisoning and Algal Blooms | 928 | ||
Myelopathies from Dietary Dependence on Neurotoxic Plants | 929 | ||
Neurodegenerative Diseases | 929 | ||
Conclusions | 930 | ||
Acknowledgements | 930 | ||
References | 930 | ||
Chapter 80 - Craniovertebral Junction Anomalies | 933 | ||
Introduction | 933 | ||
Anatomy | 933 | ||
Atlanto-Occipital Joints | 933 | ||
Atlanto-Axial Joints | 933 | ||
Ligamentous Connections | 933 | ||
Blood Supply of the Odontoid | 934 | ||
Atlas | 934 | ||
Axis | 935 | ||
Genetics | 936 | ||
Hox Genes: The Control of Rostrocaudal Specification | 936 | ||
Pax-1: The Resegmentation Gene | 936 | ||
CV junction anomalies | 936 | ||
Classification | 936 | ||
Radiological Measurement | 936 | ||
Kinematics | 938 | ||
Rotation | 938 | ||
Flexion–Extension | 939 | ||
Lateral Bending and Translational Movements | 939 | ||
Coupling | 939 | ||
Basilar Invagination | 939 | ||
Topographic Types of Basilar Invagination | 939 | ||
Clinical features | 940 | ||
Basilar Impression (Secondary Basilar Invagination) | 940 | ||
Atlanto-Axial Dislocation (Atlanto-Axial Instability) | 940 | ||
Classification | 940 | ||
Greenberg’s classification | 940 | ||
Wadia’s classification | 941 | ||
Congenital Odontoid Anomalies | 941 | ||
Os Odontoideum | 941 | ||
Clinical Features of Atlanto-Axial Instability | 942 | ||
Radiological Diagnosis of AAD | 943 | ||
Tuberculosis of the Craniovertebral Junction | 943 | ||
Clinical Presentation | 943 | ||
Aetiopathogenesis | 944 | ||
Investigations and diagnosis | 944 | ||
Management of CVJ TB | 944 | ||
Rheumatoid Arthritis | 945 | ||
Pathology (Rheumatoid Arthritis) | 945 | ||
Down Syndrome | 945 | ||
Inborn Errors of Metabolism | 946 | ||
Occipitalization or Assimilation of Atlas | 946 | ||
Klippel–Feil Syndrome | 946 | ||
Anomalies of Ring of Atlas | 947 | ||
Occipito-Atlantal Instability | 947 | ||
Traumatic Lesions Involving the Occipito-Atlanto-Axial Complex | 947 | ||
Clinical features of craniovertebral anomalies | 949 | ||
Age | 949 | ||
Familial Incidence | 949 | ||
Precipitating Factors | 949 | ||
Clinical Presentations | 949 | ||
Associated Congenital Malformations | 951 | ||
Skeletal Traction | 951 | ||
Reducible Lesions | 951 | ||
Posterior Decompression | 951 | ||
Management of Atlanto-Axial Dislocation and Basilar Invagination | 952 | ||
References | 957 | ||
Index | 961 | ||
Back Cover | Back Cover |