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Neurology in Tropics (E-book)

Neurology in Tropics (E-book)

Jagjit Chopra | Indermohan Sawhney

(2015)

Additional Information

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
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