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Nelson Pediatric Symptom-Based Diagnosis E-Book

Nelson Pediatric Symptom-Based Diagnosis E-Book

Robert M. Kliegman | Patricia S Lye | Brett J. Bordini | Heather Toth | Donald Basel

(2017)

Additional Information

Book Details

Abstract

Nelson Pediatric Symptom-Based Diagnosis uses a unique, step-by-step, symptom-based approach to differential diagnosis of diseases and disorders in children and adolescents. Conveniently linked to the world’s best-selling pediatric reference, Nelson Textbook of Pediatrics, 20th Edition, it focuses on the symptoms you’re likely to see in general practice, as well as uncommon disorders. You’ll find clear guidance on exactly what to consider and how to proceed when faced with a host of common symptoms such as cough, fever, headache, chest pain, gait disturbances, and many more.

  • Features a practical, symptom-based approach that enables you to form an accurate diagnosis.
  • Uses the same consistent, step-by-step presentation in every chapter: History, Physical Examination, Diagnosis (including laboratory tests), Imaging, Diagnosis, and Treatment.
  • Covers new approaches to diagnostic imaging and genetic testing, new diagnostic guidelines, BRUE (brief resolved unexplained event), stroke in children, behavior disorders, syncope, recurrent fever syndromes, and much more.
  • Includes full-color illustrations, algorithms, tables, and "red flags" to aid differential diagnosis.
  • Serves as an ideal companion to Nelson Textbook of Pediatrics, 20th Edition.

Table of Contents

Section Title Page Action Price
Front Cover cover
Inside Front Cover ifc1
Nelson Pediatric Symptom-Based Diagnosis i
Copyright Page iv
Dedication v
Contributors vii
Preface ix
Table Of Contents xi
1 Respiratory Disorders 1
1 Sore Throat 1
Viral Pharyngitis 1
Infectious Mononucleosis 4
Pathogenesis 4
Clinical Features 4
Diagnosis 4
Group A Streptococcal Infection 6
Epidemiology 6
Clinical Features 6
Scarlet Fever 7
Diagnosis 7
Treatment 8
Suppurative Complications 9
Nonsuppurative Sequelae 10
Treatment Failure and Chronic Carriage 11
Recurrent Acute Pharyngitis 12
Infection With Streptococci That Are Not Group A (Non-A Streptococci) 12
Fusobacterium Necrophorum 12
Arcanobacterium Infection 12
Epiglottitis and Bacterial Tracheitis 13
Diphtheria 13
Pathogenesis 14
Clinical Features 14
Diagnosis 14
Gonococcal Pharyngitis 14
Chlamydial and Mycoplasmal Infections 14
Summary and Red Flags 14
References 14
References 14.e1
Group A Streptococci 14.e1
Other Causes 14.e1
Complications 14.e1
Treatment 14.e1
2 Cough 15
Introduction 15
Pathophysiology 15
History 15
Demographics 15
Characteristics of the Cough 15
Associated Symptoms 15
Family and Patient’s Medical History 15
Physical Examination 16
Inspection 16
Fingers. 16
Chest, abdomen, and spine. 16
Palpation 17
Percussion 18
Auscultation 19
Diagnostic Studies 20
Radiography 20
Hematology/Immunology 20
Bacteriology/Virology 22
Other Tests 22
Differential Diagnosis and Treatment 22
Infection 22
Infections in infants. 22
Viral upper respiratory infections (URI). 22
Croup (laryngotracheobronchitis). 23
Bronchiolitis. 23
Viral pneumonia. 23
Pertussis (whooping cough). 23
Chlamydial infection. 24
Ureaplasmal infection. 24
Bacterial pneumonia. 24
Infections in toddlers and children 24
Viral URIs. 24
Sinusitis. 24
Pneumonia. 26
Tuberculosis. 28
Aspiration 29
Foreign Body 29
Gastroesophageal Reflux 29
Asthma 30
Cystic Fibrosis 30
Anatomic Abnormalities 32
Vascular rings and slings. 32
Pulmonary sequestration. 32
Congenital pulmonary airway malformation (CPAM). 32
Congenital lobar emphysema. 32
Tracheoesophageal fistula. 33
Hemangiomas. 33
Enlarged lymph nodes. 33
Bronchial stenosis. 35
Bronchogenic cysts. 35
Habit (Psychogenic) Cough 35
Other Causes of Cough 36
Bronchiectasis. 36
Ciliary dyskinesia. 36
Interstitial lung disease. 36
Pulmonary hemosiderosis. 36
Tumors. 36
Tracheomalacia and bronchomalacia. 36
Spasmodic croup. 36
Obliterative bronchiolitis. 36
Hemoptysis 36
When Cough Itself Is a Problem 38
Summary and Red Flags 38
References 38
References 38.e1
Cough 38.e1
Upper Respiratory Infection 38.e1
Pneumonia 38.e1
Foreign Bodies 38.e1
Cystic Fibrosis 38.e1
Asthma 38.e1
Hemoptysis 38.e1
3 Respiratory Distress 39
Introduction 39
Diagnostic Approach 39
History 39
Physical Examination 39
Pulmonary Physical Examination 39
Other Parts of the Physical Examination 41
Laboratory Tests 41
Imaging 41
Radiography 41
Computed Tomography 42
Magnetic Resonance Imaging 43
Fluoroscopy 43
Endoscopy 43
Causes of Respiratory Distress 43
Wheezing 43
Asthma 44
Bronchiolitis 47
Mycoplasma pneumoniae Infections 48
Vocal Cord Dysfunction 48
Foreign Body Aspiration 49
Stridor 50
Croup 50
Bacterial Tracheitis 51
Epiglottitis 53
Laryngomalacia 54
Vocal Cord Paralysis 54
Vascular Rings 54
Subglottic Stenosis 55
Cough 56
Viral and Bacterial Pneumonia 56
Hypersensitivity Pneumonitis 57
Allergic Bronchopulmonary Aspergillosis 57
Other Causes of Respiratory Distress 58
Aspiration of Oropharyngeal Contents 58
Gastroesophageal Reflux 59
Pneumothorax 59
Cystic Fibrosis 59
Dyskinetic Cilia Syndrome 59
Nonpulmonary Causes of Respiratory Distress 59
Cardiac 59
Neurologic 60
Other 60
Summary and Red Flags 60
References 60
References 60.e1
General 60.e1
Wheezing 60.e1
Stridor 60.e1
Cough 60.e1
4 Earache 61
Introduction 61
History 61
Physical Examination 61
Diagnostic Tests 65
Bacterial Cultures 65
Tympanometry 65
Acoustic Reflectometry 66
Diagnostic Imaging 66
Differential Diagnosis 66
Otitis Externa 67
Malignant Otitis Externa 67
Acute Otitis Media 68
Bacteriology/Virology 68
Treatment 68
Patients With Persistent Symptoms 71
Recurrent Acute Otitis Media 71
Otitis Media With Effusion 71
Mastoiditis 72
Cholesteatoma 72
Intracranial Complications 72
Summary and Red Flags 74
References 74
References 74.e1
5 Apparent Life Threatening Event–Brief Resolved Unexplained Event 75
Definition 75
Epidemiology 75
Etiology 75
Clinical Evaluation 75
History 75
Physical Examination 76
Diagnostic Evaluation 77
Differential Diagnosis by System 79
Gastrointestinal 79
Infectious Disease 79
Neurologic 80
Airway/Pulmonary 81
Child Maltreatment 81
Cardiac 81
Metabolic/Genetic 82
Summary and Red Flags 82
References 82
References 82.e1
Apparent Life-Threatening Event 82.e1
Brief Resolved Unexplained Event 82.e1
Gastrointestinal 82.e1
Infectious 82.e1
Neurologic 82.e1
Airway/Pulmonary 82.e1
Child Maltreatment 82.e1
Cardiac 82.e1
2 Cardiac Disorders 83
6 Syncope and Dizziness 83
Syncope 83
Neurocardiogenic Syncope 84
Orthostatic Syncope 84
Postural Orthostatic Tachycardia Syndrome (Pots) 85
Cardiac Syncope/Sudden Cardiac Death 87
Neurologic Causes of Syncope-Like Episodes 90
Metabolic Causes of Syncope 92
Psychiatric Causes of Syncope 92
Evaluation of the Syncopal Child 92
History 92
Physical Examination 92
Diagnostic Tests 92
Summary and Red Flags 92
Vertigo 92
Evaluation of the Patient with Vertigo 94
History 94
Physical Examination 95
Diagnostic Tests 95
Summary and Red Flags 95
Disequilibrium 95
Evaluation of the Patient with Disequilibrium 98
History 98
Physical Examination 99
Diagnostic Tests 99
Summary and Red Flags 99
Lightheadedness 101
Evaluation of the Patient with Lightheadedness 102
History 102
Physical Examination 102
Diagnostic Tests 103
Summary and Red Flags 103
References 103
References 103.e1
General 103.e1
Syncope 103.e1
Vertigo 103.e1
Disequilibrium 103.e1
Lightheadedness 103.e1
7 Chest Pain 104
Causes of Chest Pain 104
Approach to the Patient With Chest Pain 104
History 104
Musculoskeletal 106
Respiratory 106
Psychogenic/Idiopathic 107
Gastrointestinal 108
Other 108
Cardiac 111
Physical Examination 112
Electrocardiogram 114
Further Diagnostic Testing 114
Treatment 115
References 115
References 115.e1
8 Murmurs 116
Thorax 116
Origins of the Heart Sounds 116
Cardiac Cycle 116
Changes in the Circulation at Birth 116
Normal Intracardiac Pressures 117
Pediatric Cardiovascular Evaluation 117
History 117
Symptoms and Signs of Heart Disease 119
Physical Examination 119
Overall Appearance 119
Vital Signs 120
Respiratory Assessment 122
Cardiovascular Assessment 122
Arterial Examination 122
Venous Examination 122
Precordial Examination 122
Auscultation 122
Heart Sounds 123
First Heart Sound 123
Second Heart Sound 123
Third Heart Sound 124
Fourth Heart Sound 124
Ejection Click 124
Opening Snap 124
Non-Ejection Click 124
Classification of Cardiac Murmurs 124
Pediatric Murmur Evaluation 125
Systolic Murmurs 125
Diastolic Murmurs 125
Continuous Murmurs 125
Murmurs in Children With Normal Hearts 127
Vibratory Still Murmur 127
Pulmonary Flow Murmur 127
Peripheral Pulmonary Arterial Stenosis Murmur 127
Supraclavicular or Brachiocephalic Systolic Murmur 127
Aortic Systolic Murmur or “Athlete’s Murmur” 128
Normal Continuous Murmurs 128
Venous Hum 128
Mammary Arterial Soufflé 128
Physical Examination of Common Lesions With Left-to-Right Shunt 128
Atrial Septal Defects 128
Patent Ductus Arteriosus 129
Ventricular Septal Defects 129
Size 129
Location 130
Shunt Flow 130
Pulmonary Hypertension 130
Associated Anomalies 130
Complete Atrioventricular Septal Defects 131
Physical Examination of Common Lesions With Right-to-Left Shunt: Cyanosis 131
Tetralogy of Fallot 131
Tricuspid Valve Atresia 132
Pulmonary Atresia With Intact Ventricular Septum 133
Transposition of the Great Arteries 133
Hypoplastic Left Heart Syndrome 134
Physical Examination of Common Lesions With Simple Obstruction 134
Pulmonary Valve Stenosis 134
Aortic Valve Stenosis 134
Coarctation of the Aorta 136
Mitral Valve Stenosis 136
Atrioventricular Valve and Semilunar Valve Insufficiency 137
Tricuspid Valve Regurgitation 137
Mitral Valve Insufficiency 137
Mitral Valve Prolapse 137
Pulmonary Valve Insufficiency 138
Aortic Valve Insufficiency 138
Miscellaneous Cardiac Anomalies 139
Pericardial Disease 139
Pulmonary Hypertension 139
Approach to Congenital Heart Disease 139
Acute Rheumatic Fever and Rheumatic Heart Disease 140
Infective Endocarditis 140
Summary and Red Flags 143
References 143
References 143.e1
Introduction 143.e1
Origins of Heart Sounds 143.e1
Cardiovascular Assessment 143.e1
Murmurs in Children with Normal Hearts 143.e1
Vibratory Still Murmur 143.e1
Peripheral Pulmonary Arterial Stenosis 143.e1
The Supraclavicular Murmur 143.e1
Aortic Systolic Murmur 143.e1
Venous Hum 143.e1
Mammary Arterial Soufflé 143.e1
Congenital Heart Disease 143.e1
Acute Rheumatic Fever and Rheumatic Heart Disease 143.e1
Infective Endocarditis 143.e2
3 Gastrointestinal Disorders 144
9 Failure to Thrive 144
Normal Growth 144
Definitions 144
Interpretation of Growth Charts 145
Epidemiology 146
Clinical Presentation 146
Approach to Determining Etiology 147
History 148
History of the Present Illness 149
Medical History 150
Family History 150
Social History 151
Review of Systems 151
Physical Examination 152
Laboratory Evaluation 152
Overall Approach to Management 154
Steps to Improve Calorie Intake 154
Mealtime Behavior 154
Beverages 154
Food Selection 155
Daily Routines and Snacks 157
Calculating Caloric Need 157
Nutritional Supplementation for the Older Infant and Child 158
Referral Resources and Other Options 158
Multidisciplinary Team 158
Recording or Direct Observation 158
Involvement of Social Service Agencies 158
Behavioral Strategies 159
Non-Oral Enteral Feeding 159
Children With Special Health Care Needs 159
Criteria for Hospitalization 159
Monitoring 159
Long-Term Outcomes 160
Summary and Red Flags 160
References 160
References 160.e1
Reviews 160.e1
Treatment and Outcomes 160.e1
10 Abdominal Pain 161
Pathophysiology of Abdominal Pain 161
Visceral Pain 161
Parietal Pain 161
Acute Abdominal Pain 161
History 161
Essential Components of the History 161
Time of onset of pain. 161
Location of pain. 162
Character of pain. 162
Child’s activity level. 162
Gastrointestinal symptoms. 163
Associated symptoms. 166
Family history and personal medical history. 166
Physical Examination 166
Laboratory Evaluation 169
Complete Blood Cell Count 169
Urinalysis 169
Other Laboratory Tests 169
Imaging Evaluation 169
Plain Radiography 170
Ultrasonography 170
Contrast Studies 170
Computed Tomography 171
Management 171
Specific Causes of Acute Abdominal Pain 171
Appendicitis 171
Diagnosis 172
Laboratory and Radiographic Testing 172
Treatment 173
Pancreatitis 173
Manifestations 173
Complications 174
Management 174
Cholelithiasis 175
Diagnosis 176
Treatment 176
Peptic Ulcer Disease 176
Chronic Abdominal Pain 176
Making a Diagnosis of Functional Abdominal Pain 178
Severity and Location of Pain 179
Approach to Treatment 179
Red Flags 180
References 181
References 181.e1
Acute Abdominal Pain 181.e1
Peptic Ulcer Disease 181.e1
Appendicitis 181.e1
Pancreatitis 181.e1
Hepatobiliary Tract Disease 181.e1
Chronic Abdominal Pain 181.e2
11 Diarrhea 182
Acute Diarrhea 182
History 182
Physical Examination 182
Viral Diarrhea 182
Rotavirus infection. 182
Norovirus infection. 182
Bacterial Diarrhea 184
Salmonella infection. 184
Shigella infection. 184
Campylobacter infection. 184
Yersinia infection. 184
Escherichia coli infection. 185
Clostridium difficile infection. 187
Aeromonas infection. 187
Plesiomonas infection. 187
Parasitic Diarrhea 188
Giardiasis. 188
Entamoeba histolytica infection. 188
Cryptosporidium infection. 188
Other Causes of Acute Diarrhea 188
Parenteral secondary diarrhea. 188
Medications. 188
Food poisoning (Table 11.9; see Fig. 11.1). 188
Chronic Diarrhea 188
History 188
Physical Examination 190
Diagnostic Evaluation 190
Disorders of Carbohydrate Malabsorption 190
Disaccharidase Deficiency 191
Congenital sucrase-isomaltase deficiency (CSID). 191
Maltase-glucoamylase deficiency. 193
Congenital glucose-galactose malabsorption (CGGM). 193
Congenital lactase deficiency. 193
Primary lactase deficiency (lactose intolerance). 193
Secondary lactase deficiency. 194
Chronic NonSpecific Diarrhea 194
Small Intestinal Bacterial Overgrowth (SIBO) 194
Irritable Bowel Syndrome (IBS) 197
Celiac Disease 198
Inflammatory Bowel Disease (IBD) 199
Clinical presentation. 199
Diagnosis. 199
Summary and Red Flags 203
References 203
References 203.e1
Acute Gastroenteritis 203.e1
Chronic Diarrhea 203.e1
12 Vomiting and Regurgitation 204
Definitions 204
Neuroanatomy of Vomiting 204
Data to Guide the Diagnosis 204
History 204
Demographics 204
Characteristics of Vomiting 204
Associated symptoms. 205
Medical, family, and social history. 205
Physical Examination 205
Abdominal Examination 205
Rectal Examination 208
Laboratory Data 208
Radiographic and Procedure Data 208
Differential Diagnosis 208
General Approach 208
Gastrointestinal Obstruction 210
Esophageal Obstruction 210
Esophageal atresia. 210
Esophageal stenosis. 210
Esophageal strictures. 210
Pyloric Stenosis 210
Intestinal Obstruction 210
Duodenal atresia, stenosis, and web; annular pancreas. 215
Duodenal hematoma. 215
Jejunal atresia, ileal atresia, and ileal stenosis. 215
Intestinal strictures. 215
Adhesions. 215
Duplications. 215
Meconium ileus and distal intestinal obstruction syndrome (DIOS). 216
Incarcerated hernia. 216
Malrotation and volvulus. 216
Meckel diverticulum. 217
Intussusception. 217
Superior mesenteric artery syndrome. 217
Constipation, meconium plug, and anal stenosis. 218
Gastrointestinal Dysmotility 218
Achalasia 218
Gastroesophageal Reflux 218
Gastric Stasis and Gastroparesis 218
Ileus 218
Pseudoobstruction 219
Gastrointestinal Inflammation 219
Esophagitis 219
Gastroenteritis 219
Peptic Ulcer Disease 220
Meckel Diverticulitis 220
Mesenteric Adenitis 220
Appendicitis 220
Inflammatory Bowel Disease 220
Allergic Enteropathy, Eosinophilic Gastroenteropathy, and Eosinophilic Esophagitis 220
Gastrointestinal Ischemia and Vascular Insufficiency 221
Abdominal Migraine 221
Vasculitis 221
Volvulus and Intussusception 221
Mesenteric Ischemia 221
Gastrointestinal Perforation and Peritonitis 221
Hepatobiliary Disorders 221
Hepatitis 221
Biliary Colic and Cholecystitis 222
Pancreatitis 222
Gynecologic and Urologic Disorders 222
Pyelonephritis 222
Ureteropelvic Junction Obstruction and Hydronephrosis 222
Renal Colic 222
Dysmenorrhea, Endometriosis, and Pelvic Inflammatory Disease 222
Ovarian Torsion 222
Hyperemesis Gravidarum 222
Testicular Torsion 222
Respiratory Disorders 222
Sinusitis, Pharyngitis, and Otitis 222
Pneumonia 222
Central Nervous System Disorders 222
Increased Intracranial Pressure 222
Abdominal Epilepsy 222
Vestibular Disorders, Motion Sickness 223
Ventriculoperitoneal Shunt Complications 223
Psychobehavioral Disorders 223
Psychogenic Vomiting 223
Rumination 223
Eating Disorders 223
Management 223
Metabolic Disorders 223
Poisonings and Drugs 223
Hematemesis 223
Other Causes of Vomiting 224
Chemotherapy 224
Radiation Therapy 224
Cyclic Vomiting 224
Porphyria 225
Familial Mediterranean Fever (Benign Paroxysmal Peritonitis, Periodic Peritonitis, Polyserositis) 225
Familial Dysautonomia 225
Complications of Vomiting 225
Metabolic Complications 225
Nutritional Complications 225
Mallory-Weiss Tear 225
Peptic Esophagitis 225
Therapy 232
Treatment of Behavioral Aspects 232
Antiemetic Drugs 232
Summary and Red Flags 234
References 234
References 234.e1
General 234.e1
Gastrointestinal Obstruction 234.e1
Gastroesophageal Reflux 234.e1
Other Etiologies 234.e1
Therapy 234.e1
13 Gastrointestinal Bleeding 235
Definitions 235
Hematemesis 235
Hematochezia and melena 235
Approach to Gastrointestinal Bleeding 235
Hematemesis and Melena: Upper Gastrointestinal Bleed 235
History 235
Physical Examination 236
Differential Diagnosis 237
Hematochezia: Lower Gastrointestinal Bleed 238
History 238
Physical Examination 238
Differential Diagnosis 238
Occult Blood Loss 239
Laboratory Evaluation 239
Imaging 239
Radiographs 239
Abdominal Ultrasound 240
Computed Tomography 240
Magnetic Resonance Enterography 240
Angiography 240
Nuclear Imaging 240
Imaging 241
Capsule Endoscopy 241
Treatment 241
Resuscitation 241
Vasoactive Agents 242
Endoscopic Modalities 243
Interventional Radiology 243
Summary and Red Flags 243
References 243
References 243.e1
14 Hepatomegaly 244
Assessment of the Liver 244
History and Physical Examination 244
Pathophysiology 246
Evaluation of the Child With Hepatomegaly 246
Laboratory Studies 246
Hepatocellular Injury 247
Biliary Injury 247
Exocrine Function 247
Synthetic Function 247
Metabolic Function 247
Extrahepatic Involvement 248
Imaging Studies 249
Liver Biopsy 249
Specific Issues in the Diagnosis and Treatment of Hepatomegaly 249
Hepatomegaly in the Infant 249
Hepatomegaly in the Child and Adolescent 251
Steatohepatitis 251
Viral Hepatitis 251
Toxins 252
Alpha-1-Antitrypsin Deficiency 252
Wilson Disease 252
Autoimmune Liver Disease 252
Primary Sclerosing Cholangitis 252
Acquired Immunodeficiency Syndrome 253
Other Infections 253
Fitz-Hugh–Curtis Syndrome 253
Hepatic Abscess 253
Endocrine Disorders 253
Liver Tumors 253
Hepatic Cysts 254
Hepatic Venous Outflow Obstruction 254
Summary and Red Flags 254
References 254
References 254.e1
General Review 254.e1
Clinical Assessment of Liver Size 254.e1
Biochemical Studies of Liver Function and Injury 254.e1
Neonatal Cholestasis 254.e1
Viral Hepatitis 254.e1
Metabolic Liver Disease 254.e1
Autoimmune Liver Disease 254.e1
Liver Tumors 254.e1
Miscellaneous Disorders Causing Hepatomegaly 254.e1
15 Jaundice 255
Diagnostic Strategies 255
Bilirubin 255
Aminotransferases 255
Alkaline Phosphatase 255
γ-Glutamyltransferase 259
Bile Acids 259
Albumin 259
Prothrombin Time 259
Ultrasonography 259
Scintigraphy 259
Computed Tomography 259
Magnetic Resonance 259
Endoscopic Retrograde Cholangiopancreatography 259
Percutaneous Transhepatic Cholangiography 259
Liver Biopsy 259
Jaundice in the Neonate and Infant 260
History 260
Physical Examination 261
Differential Diagnosis 261
Physiologic and Breast Milk Jaundice 261
Unconjugated Hyperbilirubinemia 263
Polycythemia. 263
Hemolytic disorders. 264
Isoimmune hemolytic disease. 264
Erythrocyte membrane defects. 264
Other considerations. 264
Familial disorders of bilirubin metabolism 264
Gilbert syndrome. 264
Crigler-Najjar syndrome. 264
Lucey-Driscoll syndrome. 264
Therapy. 265
Neonatal Conjugated Hyperbilirubinemia 265
Obstructive/anatomic abnormalities, idiopathic cholestasis, and idiopathic neonatal hepatitis 265
Biliary atresia. 265
Alagille syndrome. 266
Choledochal cysts. 266
Treatable infections 267
Bacterial infection. 267
Herpes simplex. 267
Enteroviruses. 267
Cytomegalovirus infection. 267
Hepatitis B. 267
Syphilis. 267
Toxoplasmosis. 267
Treatable metabolic disorders. 267
Galactosemia. 267
Other identifiable infectious and metabolic causes of cholestasis 268
α1-Antitrypsin deficiency. 268
Cystic fibrosis. 268
Hypothyroidism and hypopituitarism. 268
Progressive Familial Intrahepatic Cholestasis 268
Idiopathic neonatal hepatitis. 269
Treatment of cholestasis. 269
Jaundice in the Child and Adolescent 269
History 269
Physical Examination 269
Differential Diagnosis 269
Unconjugated Hyperbilirubinemia 269
Conjugated Hyperbilirubinemia 270
Obstruction. 270
Gallstones. 270
Primary sclerosing cholangitis. 270
Infection. 271
Hepatitis A. 272
Hepatitis B. 272
Hepatitis C. 272
Hepatitis D. 273
Hepatitis E. 273
Epstein-Barr virus. 273
Other viruses. 273
Wilson disease. 273
Drugs and toxins. 273
Autoimmune hepatitis. 273
Summary and Red Flags 274
References 274
References 274.e1
General 274.e1
Diagnostic Strategies 274.e1
Neonatal Jaundice 274.e1
Alagille Syndrome, Primary Intrahepatic Cholestasis 274.e1
α1-Antitrypsin Deficiency 274.e1
Biliary Atresia 274.e1
Crigler-Najjar Syndromes 274.e1
Cystic Fibrosis 274.e1
Erythrocyte Enzyme Defects 274.e1
Gilbert Syndrome 274.e1
Lucey-Driscoll Syndrome 274.e1
Physiologic and Breast Milk Jaundice 274.e1
Jaundice in Older Children and Adolescents 274.e1
Autoimmune Hemolytic Anemia 274.e1
Autoimmune Hepatitis 274.e1
Drugs 274.e1
Gallstones 274.e1
Hepatitis 274.e1
Primary Sclerosing Cholangitis 274.e1
Wilson Disease 274.e1
16 Constipation 275
Physiology of Normal Defecation and Constipation 275
Data Collection and Assessment 275
History 275
Physical Examination 277
Diagnostic Evaluation 278
Differential Diagnosis 278
Hirschsprung Disease 278
Chronic Intestinal Pseudoobstruction 281
Anterior Anal Displacement 281
Anal Stenosis 281
Imperforate Anus 281
Spina Bifida and Spina Bifida Occulta 281
Metabolic Diseases 281
Neurologic Disease 282
Medication-Related Constipation 282
Encopresis 282
Summary and Red Flags 282
References 282
References 282.e1
17 Abdominal Masses 283
Diagnostic Strategies 283
Clinical History 283
Physical Examination 283
Laboratory and Imaging Studies 285
Splenomegaly 286
History 287
Physical Examination 289
Approach to the Child with Splenomegaly 289
Laboratory Investigation 289
Complete Blood Cell Count 289
Leukocyte Count and Differential. 289
Hemoglobin, Erythrocyte Morphology, and Reticulocyte Count. 289
Platelet Count. 289
Pancytopenia. 289
Erythrocyte Sedimentation Rate 289
Liver Function Tests 291
Immunologic Evaluation 291
Viral Antibody Titers 291
Cultures 291
Bone Marrow Examination 291
Imaging 292
Splenectomy 292
Neuroblastoma 292
Renal Masses 294
Congenital Hydronephrosis 294
Cystic Abnormalities of the Kidney 294
Wilms Tumor (Nephroblastoma) 295
Liver Tumors 295
Hepatoblastoma 295
Hepatocellular Carcinoma 296
Congenital Dilatation of the Bile Ducts 296
Intestinal and Pancreatic Masses 296
Appendiceal Phlegmon and Abscess 296
Bezoar 298
Duplications 298
Neoplasms of the Gastrointestinal Tract 298
Mesenteric, Omental, and Retroperitoneal Cysts 299
Pancreatic Pseudocyst and Neoplasms 299
Ovarian Tumors 300
Summary and Red Flags 301
References 301
References 301.e1
Diagnostic Strategies 301.e1
Splenomegaly 301.e1
Neuroblastoma 301.e1
Renal Masses 301.e1
Wilms Tumor 301.e1
Liver Tumors 301.e1
Congenital Dilatation of the Bile Ducts 301.e1
Intestinal and Pancreatic Masses 301.e1
Duplications 301.e1
Ovarian Tumors 301.e2
4 Genitourinary Disorders 302
18 Dysuria 302
Neonates 302
Children 2-24 Months of Age 302
Preschool Children 304
School-Aged/Prepubertal Children 304
Adolescents 305
Summary and Red Flags 310
References 311
References 311.e1
19 Proteinuria 312
Nephrotic Syndrome in Young Children 312
Differential Diagnosis 312
Minimal Change Disease 314
Diagnosis 314
Treatment 315
Complications of Nephrotic Syndrome 316
Infection. 316
Thrombosis. 317
Hyperlipidemia. 317
Other Forms of Nephrotic Syndrome 317
Focal Segmental Sclerosis 317
Diagnosis 317
Treatment 317
Membranous Nephropathy 317
Treatment 318
Nephrotic Syndrome in Infants Younger Than 1 Year 318
Congenital Nephrotic Syndrome 318
Diffuse Mesangial Sclerosis 318
Asymptomatic Proteinuria Disorders 318
Summary and Red Flags 320
References 320
References 320.e1
20 Hematuria 321
Gross Hematuria 321
History 321
Physical Examination 323
Evaluation 323
Laboratory Tests 323
Imaging and Cystoscopy 325
Microscopic Hematuria 325
More Common Causes of Hematuria 326
Postinfectious Glomerulonephritis 326
Immunoglobulin A (IgA) Nephropathy 326
Hereditary Nephritis 327
Polycystic Kidney Disease 327
Uncommon Causes of Hematuria in Childhood 327
Red Flags 328
References 329
References 329.e1
21 Acute and Chronic Scrotal Swelling 330
Scrotal and Inguinal Anatomy 330
Inguinal Region 330
Testis Descent 330
Scrotum 330
Testis 330
Diagnostic Strategies 330
History 330
Physical Examination 331
Pubertal development. 331
Scars in the inguinal region. 331
Scrotal skin changes and fixation. 331
Testis position within the scrotum. 332
Cremasteric reflex. 332
Laboratory Data 332
Imaging Studies 332
Differential Diagnosis 333
Testicular Torsion 333
Torsion of the Appendix Testis 334
Epididymitis, Epididymoorchitis, and Orchitis 335
Trauma and Hematocele 335
Varicocele 336
Inguinal Hernia 336
Hydrocele 336
Testicular Tumors 337
Meconium Peritonitis 338
Scrotal Wall Swelling 338
Henoch-Schönlein Purpura 338
Acute Idiopathic Scrotal Wall Edema 338
Idiopathic Fat Necrosis 338
Fournier Gangrene 338
Referred Pain 338
Red Flags 338
References 338
References 338.e1
Testicular Torsion 338.e1
Torsion of the Appendix Testis 338.e1
Epididymoorchitis 338.e1
Trauma 338.e1
Varicocele 338.e1
Testicular Tumors 338.e1
Other Diagnoses 338.e1
Diagnostic Strategies 338.e2
Imaging 338.e2
22 Menstrual Problems and Vaginal Bleeding 339
Prepubertal Vaginal Bleeding 339
Abnormal Bleeding in Adolescence 341
Review of the Menstrual Cycle 341
Pregnancy 342
Coagulopathy 342
Ovulatory Dysfunction 342
Endometrial Causes 344
Iatrogenic Causes 344
Not Yet Classified 344
Structural Causes: PALM 344
Congenital Anomalies 345
Treatment 345
Menstrual Pain in Adolescents 346
Summary and Red Flags 347
References 347
References 347.e1
23 Disorders of Sex Development 348
Overview of Sex Differentiation 348
Overview of Gonadal Function 348
Testes 348
Ovaries 351
Diagnostic Approach to the Patient With Atypical or Ambiguous Genitalia 356
Basic Approaches to the Diagnosis and Management of Disorders of Sex Development 358
Specific Types of Disorders of Sex Development 359
46,XX Disorders of Sex Development 359
Androgen Exposure/Fetoplacental Source 359
Congenital adrenal hyperplasia. 359
Aromatase deficiency. 360
Cortisol resistance due to glucocorticoid receptor gene mutation. 360
Androgen Exposure: Maternal Source 360
Virilizing maternal tumors. 360
Administration of androgenic drugs to women during pregnancy. 360
Disorders of Ovarian Development 360
46,XX testicular DSD. 360
46,XX gonadal dysgenesis. 360
Undetermined/unknown. 361
46,XY Disorders of Sex Development 361
Defects in Testicular Development 361
Wilms tumor suppressor gene (WT1) mutations: Denys-Drash, Fraser and WAGR syndromes. 361
Campomelic syndrome. 361
Steroidogenic Factor 1 (SF1) Gene Mutations 361
Other Known Genetic Causes of 46,XY DSD 361
XY pure gonadal dysgenesis (Swyer syndrome). 361
XY gonadal agenesis syndrome (embryonic testicular regression syndrome). 361
Deficiency of Testicular Hormone Production 362
Leydig cell aplasia. 362
Congenital adrenal hyperplasia (CAH). 362
Deficiency of 17-ketosteroid reductase. 362
Persistent müllerian duct syndrome. 363
Smith-Lemli-Opitz syndrome. 363
Defects in Androgen Action 363
Dihydrotestosterone deficiency. 363
Androgen receptor defects: androgen insensitivity syndromes (AISs). 364
Undetermined Causes of 46,XY Disorders of Sex Development 365
Ovotesticular Disorders of Sex Development 365
Sex Chromosome Disorders of Sex Development 366
Red Flags 366
References 366
References 366.e1
5 Developmental and Psychiatric Disorders 367
24 Intellectual and Developmental Disability 367
Definitions 367
Epidemiology 367
Intellectual Disability 367
Developmental Disability 367
Diagnosis 368
Identification 368
Developmental Risk Factors 369
Developmental Protective Factors 369
Screening for Specific Abnormalities 370
Visual Deficits 370
Loss of Hearing 370
Speech and Language Disorders 370
Other Conditions 371
Prenatal and Newborn Screening Programs 371
Prenatal Screening 371
Newborn Screening 371
Identification of Children With Developmental Disabilities in Primary Health Care Settings 371
Developmental Screening 372
Developmental Surveillance 372
Comprehensive Developmental Assessment 372
Neurodevelopmental Pediatric Assessment 372
History 372
Physical Examination 375
Neurodevelopmental Examination 378
Formal Neurodevelopmental Assessments 378
Psychologic Evaluation 378
Speech-Language and Oral Motor Evaluation 378
Diagnostic Strategy 378
Laboratory Testing 379
Genetic Tests 382
Metabolic Tests 382
Neuroimaging 384
Ultrasonography 384
Computed Tomography Scans 385
Magnetic Resonance Imaging 385
Indications for Various Imaging Modalities 385
Other Tests 386
Discussing a Developmental Diagnosis with Parents 386
Specific Conditions 386
Cerebral Palsy 386
Autism Spectrum Disorder 387
Fragile X Syndrome 387
Inborn Errors of Metabolism and Storage Diseases 388
Congenital Infections 388
Postnatal Infections 388
Treatment 388
Complementary and Alternative Therapies 391
Pitfalls and Hazards in Developmental Diagnosis 391
Summary and Red Flags 392
References 392
References 392.e1
25 Dysmorphology 393
Diagnostic Approaches 393
Human Variation 393
Teratology 394
Embryogenesis 396
Birth Defects 396
Clinical Classification 396
Single-System Defects 396
Association 396
Sequence 396
Syndrome 396
Complex 396
Dysmorphic Evaluation 397
Components of Dysmorphic Evaluation 397
Detailed History 397
Family health history. 398
Pregnancy and birth history. 398
Developmental history. 401
Examination 401
Initial Inspection 403
Anthropometrics 403
Head and Neck 404
Face 405
General “Rules” 405
Assembling the Data 405
Minimal Diagnostic Criteria 405
Tools to Assist the Diagnostic Odyssey 405
Genetic Testing 408
References 410
References 410.e1
Bone Age and Physical Measurements 410.e1
Syndrome References 410.e1
26 Irritable Infant 411
Diagnostic Approach 411
Addressing Caregivers’ Response to Crying 416
Specific Diagnoses 418
Child Maltreatment 418
Infantile Colic 419
Feeding and Gastrointestinal Dysfunction 419
Teething 419
Drug Reactions 420
Summary and Red Flags 420
References 420
References 420.e1
Child Maltreatment 420.e1
Infantile Crying and Colic 420.e1
Gastrointestinal Causes of Irritability 420.e1
Teething 420.e1
Medication or Drug Reactions 420.e1
27 Unusual Behaviors 421
Conditions Characterized by Disruptive Behaviors 421
Conditions That Do Not Violate the Rights of Others 421
Attention-deficit/hyperactivity disorder. 421
Inattention 421
Hyperactivity/Impulsivity 422
Tic disorders. 424
Disruptive mood dysregulation disorder. 425
Substance Use Disorder. 425
Conditions That Violate the Rights of Others 425
Oppositional defiant disorder. 425
Conduct disorder. 425
Conditions Characterized by Disruption in Mood 426
Conditions Characterized by Depressed Mood 426
Major depressive disorder. 426
Premenstrual dysphoric disorder. 427
Substance-induced mood disorders. 427
Adjustment disorder. 427
Conditions Characterized by Extremes of Mood Lability 428
Addressing Suicidal Thoughts and Attempts 428
Conditions Characterized by Worry, Fear, and Panic 428
Conditions Characterized by Worry 428
Worry Without Unusual Behaviors 429
Adjustment disorder with anxiety. 429
Worry With Unusual Behaviors 429
Pediatric autoimmune neuropsychiatric disorders associated with Streptococcus pyogenes (PANDAS). 430
Conditions Characterized by Fear 430
Fears Arising Spontaneously 430
Specific phobias. 430
Social anxiety disorder (social phobia). 430
Separation anxiety disorder. 430
Selective mutism. 430
Fears Arising from Traumatic Events 430
Conditions Characterized by Panic 431
Panic disorder. 431
Agoraphobia. 431
Conditions Characterized by Mental Status Abnormalities 431
Conditions Characterized by Hallucinations 431
Fantasy-based hallucinations. 432
Grief-induced hallucinations. 432
Hallucinations associated with sleep. 432
Phobic hallucinations. 432
Febrile hallucinations. 432
Schizophrenia. 433
Conditions Characterized by Fluctuating Mental Status 434
Delirium. 434
Substance intoxication. 434
Serotonin syndrome. 435
Neuroleptic malignant syndrome. 435
Conditions Characterized by Persistent Delay in Development 435
Autism spectrum disorder. 435
Conditions Characterized by Physical Findings or Complaints 435
Conditions Characterized by Parental Concerns 435
Parental worry. 435
Factitious disorder imposed on another (formerly Munchausen syndrome by proxy) (see also Chapter 26). 436
Conditions Characterized by the Patient’s Physical Complaints 436
Illness anxiety disorder (hypochondriasis). 436
Somatic symptom disorder. 436
Factitious disorder. 436
Conversion disorder (functional neurologic symptom disorder). 436
Conditions Characterized by Changes in Eating or Weight 436
Anorexia nervosa. 436
Bulimia nervosa. 437
Binge eating disorder. 437
Avoidant/restrictive food intake disorder (ARFID). 437
Summary and Red Flags 438
References 438
References 438.e1
General References 438.e1
History Taking 438.e1
Disruptive Behaviors 438.e1
Mood Disorders 438.e1
Anxiety 438.e1
Altered Mental Status 438.e1
Physical Symptoms 438.e1
6 Neurosensory Disorders 439
28 Headaches 439
Introduction 439
History 439
Physical Examination 442
Neuroimaging 443
Laboratory Investigations 444
Classification of Headaches 444
Primary Headaches 444
Tension-Type Headaches 444
Migraine Headaches 447
Migraine without aura. 447
Migraine with aura. 447
Complications of migraine. 448
Trigeminal Autonomic Cephalgias 448
Cluster headache. 448
Paroxysmal Hemicrania 449
Secondary Headaches 449
Headache Associated with Trauma 449
Acute headache. 449
Persistent headache. 449
Headaches Associated with Vascular Disorders 449
Acute ischemic stroke. 449
Aneurysms and Arteriovenous Malformations 449
Arteritis, Cerebral Venous Thrombosis, and Vascular Dissection 449
Vasculitis 449
Genetic Vasculopathies 449
Headaches Associated With Nonvascular Intracranial Disorders 449
Disorders Associated with Increased CSF Pressure 450
Disorders Associated with Decreased CSF Pressure 451
Intracranial Masses 451
Headaches Associated with Epileptic Seizures 451
Chiari I Malformations 451
Headaches Related to a Substance 451
Medication-Overuse Headaches 452
Caffeine Withdrawal Headaches 452
Intracranial and Systemic Infections 452
Disorders Affecting Homeostasis 452
Headaches and/or Facial Pain Related to Dysfunction of Head and Neck Structures (Table 28.17) 452
Psychologic Factors 453
Summary and Red Flags 454
References 454
References 454.e1
29 Hypotonia, Weakness, and Stroke 455
Muscle Weakness and Hypotonia 455
Hypotonic Infant 455
Clinical Evaluation 455
Muscle Strength 455
Passive Tone 455
Joint Extensibility 457
Postural Reflexes 457
Traction response (pull-to-sit). 457
Axillary suspension. 463
Ventral suspension. 463
Diagnostic Approach 464
Common Disorders 464
Hypoxic-ischemic encephalopathy. 464
Brain malformations. 467
Uncommon Disorders 467
Progressive encephalopathies of infancy. 467
Mitochondrial diseases. 468
Brain malformation syndromes. 468
Hypotonic Older Child 468
Clinical Evaluation 468
Posture and Strength 468
Passive Tone 468
Joint Extensibility 468
Diagnostic Approach 468
Anatomic Localization 468
Is the Problem a Systemic Disorder? 472
Diagnostic Considerations 472
Common Disorders 473
Down syndrome. 473
Prader–Willi syndrome. 473
Uncommon Disorders 473
Metabolic disorders. 473
Neurologic disorders. 473
Congenital malformation syndromes. 474
Connective tissue disorders. 474
Is the Problem in the Cerebrum or Cerebellum? 475
Is the Problem in the Spinal Cord? 475
Common Disorders 475
Meningomyelocele. 475
Transverse myelitis. 476
Uncommon Disorders 476
Is the Problem in the Motor Unit? 476
Diagnostic Considerations 476
Common Disorders 476
Anterior horn cell disease. 476
Neuropathies. 477
Muscle and neuromuscular junction disorders. 478
Myopathies. 478
Neuromuscular junction disorders. 483
Stroke in Childhood 484
Neonates 488
Perinatal Ischemic Stroke 488
Polycythemia 493
Neonatal Cerebral Sinovenous Thrombosis (CSVT) 496
Intracranial Hemorrhage in the Neonate 497
Subdural Hemorrhage 497
Subarachnoid Hemorrhage 498
Intraparenchymal and Intraventricular Hemorrhage 498
Evaluation of Stroke in Infants 498
Children Aged 1-13 Years 499
Ischemic Stroke in Children 500
Congenital Heart Disease 500
Procoagulopathies 501
Autoimmune Disorders 501
Metabolic Disorders Causing Stroke 502
Moyamoya Disease 503
Sickle Cell Disease 503
Intracranial Hemorrhage 504
Coagulopathies 504
Thrombocytopenia 504
Vascular Malformations 504
Evaluation of Stroke in Children 505
Adolescents 506
Fibromuscular Dysplasia 506
Sexual Activity, Oral Contraception, and the Puerperium 506
Cocaine Use 506
Causes of Stroke Unrelated to Age 507
Pharyngeal Infection 507
Head and Neck Trauma 507
Migraine Headache 507
Summary and Red Flags 507
References 507
References 507.e1
Hypotonic Infant 507.e1
Arthrogryposis 507.e1
Hypoxic-Ischemic Encephalopathy 507.e1
Central Nervous System 507.e1
Systemic Disorders 507.e1
Spinal Muscular Atrophy 507.e1
Peripheral Neuropathy 507.e1
Neuromuscular Junction 507.e1
Myopathies 507.e2
Stroke: General 507.e2
Stroke: Neonate 507.e2
Polycythemia 507.e3
Neonatal Cerebral Venous Thrombosis 507.e3
Intracranial Hemorrhage in the Neonate 507.e3
Children Aged 1-13 Years: Congenital Heart Disease 507.e3
Children Aged 1-13 Years: Procoagulopathies 507.e3
Children Aged 1-13 Years: Autoimmune Disorders 507.e3
Children Aged 1-13 Years: Metabolic Disorders Causing Stroke 507.e3
Moyamoya Disease 507.e3
Sickle Cell Disease 507.e3
Children Aged 1-13 Years: Thrombocytopenia 507.e3
Children Aged 1-13 Years: Vascular Malformations 507.e3
Adolescents 507.e3
Causes of Stroke Unrelated to Age: Pharyngeal Infection 507.e3
Causes of Stroke Unrelated to Age: Head and Neck Trauma 507.e4
Causes of Stroke Unrelated to Age: Migraine Headache 507.e4
Causes of Stroke Unrelated to Age: Conditions Resembling Stroke 507.e4
30 Paroxysmal Disorders 508
Introduction 508
History 508
Physical Examination 508
Red Flags 509
Increased Intracranial Pressure or Large Intracranial Mass 509
Ongoing Status Epilepticus 509
Stroke or Complicated Migraine 510
Meningitis 510
Paroxysmal Spells of Altered Behavior or Movement 510
Epileptic Seizures 510
Epidemiology and Causes of Seizures and Epilepsy 510
Genetics 510
Seizure Classification and Terminology 511
Focal Seizures 512
Localization-Related Seizures, Partial Seizures 512
Generalized Seizures 515
Diagnostic Evaluation of a Seizure Disorder 515
Electroencephalographic Studies 515
Neuroimaging Studies 516
Evaluation of the First Seizure 516
Status Epilepticus 518
Classification of Epilepsies and Epileptic Syndromes 518
Neonatal Period 518
Paroxysmal Nonepileptic Disorders 518
Jitteriness. 518
Benign neonatal sleep myoclonus. 520
Acute Symptomatic Seizures and Occasional Seizures 520
Diagnostic investigations. 520
Prognosis. 520
Treatment. 521
Epileptic Syndromes 521
Benign idiopathic neonatal convulsions, familial and nonfamilial. 521
Vitamin-dependent seizures. 521
Structural focal epilepsy. 524
Early-onset generalized epileptic syndromes with encephalopathy. 524
Infancy 524
Paroxysmal Nonepileptic Disorders 524
Infantile syncope 524
Cyanotic infant syncope (breath-holding spells). 524
Pallid infant syncope. 525
Hyperekplexia. 525
Sleep disorders. 525
Shivering attacks. 525
Paroxysmal torticollis. 526
Infantile masturbation. 526
Spasmus nutans. 526
Benign paroxysmal vertigo. 527
Benign myoclonus of early infancy. 527
Alternating hemiplegia of childhood. 527
Acute Symptomatic Seizures and Occasional Seizures 527
Febrile convulsions. 527
Epileptic Syndromes 528
West syndrome 528
Evaluation: EEG, MRI. 529
Severe myoclonic epilepsy in infancy (Dravet syndrome) 529
Childhood 529
Paroxysmal Nonepileptic Disorders 529
Migraine and migraine equivalents. 529
Tic disorders 530
Sleep disorders 531
Night terrors and confusional arousals. 531
Somnambulism. 531
Self-stimulatory behavior/stereotypies. 531
Acute Symptomatic Seizures and Occasional Seizures 531
Epileptic Syndromes 531
Benign partial epilepsies of childhood. 531
Acquired epileptic aphasia and continuous spike-and-wave patterns in slow-wave sleep. 533
Symptomatic focal (localization-related) epilepsy. 534
Childhood absence epilepsy. 534
Epilepsia partialis continua and Rasmussen encephalitis. 534
Lennox-Gastaut syndrome. 535
Adolescence 535
Paroxysmal Nonepileptiform Disorders 535
Syncope. 535
Paroxysmal psychiatric events. 535
Acute Symptomatic Seizures and Occasional Seizures 536
Epileptic Syndromes 537
Juvenile myoclonic epilepsy. 537
Juvenile absence epilepsy. 537
Epilepsy with generalized tonic-clonic seizures on awakening. 537
Principles of Antiepileptic Drug Use 538
Choice of Antiepileptic Drugs 538
Focal Epilepsies 538
Focal seizures and secondary generalized tonic-clonic seizures. 538
Idiopathic Generalized Epilepsy 538
Primary generalized tonic-clonic seizures. 538
Absence seizures. 538
Myoclonic seizures. 538
Symptomatic Generalized Epilepsies 540
Tonic, atonic, and atypical absence seizures. 540
Stopping Antiepileptic Drugs 542
Lifestyle 542
References 542
References 542.e1
General 542.e1
Neonatal Period 542.e1
7 Musculoskeletal Disorders 594
33 Arthritis 594
Introduction 594
History 594
Pain Location 594
Pain Character 594
Pain Timing 596
Pain Acuity 596
Signs of Inflammation 596
Disability 596
Medical History 597
Medications 597
Family History 597
Social History 597
Review of Systems 597
Constitutional Symptoms 597
Skin Changes 598
Additional Symptoms 598
Physical Examination 600
Laboratory Studies 602
Antinuclear Antibody 602
Rheumatoid Factor 602
Additional Antibody Testing 602
Complement 603
Diagnostic Imaging 603
Radiographs 603
Magnetic Resonance Imaging (MRI) 603
Bone Scan 604
Additional Imaging Studies 604
Joint Fluid Aspiration 604
Invasive Testing 605
Juvenile Idiopathic Arthritis 606
Oligoarticular Juvenile Idiopathic Arthritis 606
Polyarticular Juvenile Idiopathic Arthritis 606
Enthesitis-Related Arthritis 606
Psoriatic Arthritis 607
Systemic Juvenile Idiopathic Arthritis 607
8 Hematologic Disorders 647
36 Lymphadenopathy and Neck Masses 647
Mechanism of Lymphadenopathy 647
History 647
Physical Examination 650
Size 650
Quality 650
Distribution 650
Differential Diagnosis 650
Differential Diagnosis of Head and Neck Lymphadenopathy: Head and Neck Masses 651
Evaluation and Management Strategies 651
Regional Lymphadenopathy 651
Generalized Lymphadenopathy 651
Lymphadenopathy Patterns 653
Infections of the oropharynx. 653
Infections of the extremities. 655
Epstein–barr virus infection. 655
Cytomegalovirus infection. 657
Cat-scratch disease. 657
Chronic granulomatous disease. 657
Human immunodeficiency virus. 657
Mycobacterial infections. 657
Toxoplasmosis. 658
Syphilis. 659
Acute leukemia, lymphoma, and other malignancies. 659
Ulceroglandular disorders. 660
Kimura disease. 660
Kikuchi-Fujimoto disease (histiocytic necrotizing lymphadenitis). 660
Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease). 660
Castleman disease. 660
Summary and Red Flags 660
References 660
References 660.e1
General References 660.e1
Medication-Related Causes of Lymphadenopathy 660.e1
Cervical Adenopathy 660.e1
Epstein–Barr Viral Infections 660.e1
Cat-Scratch Disease 660.e1
Human Immunodeficiency Virus 660.e1
Mycobacterial Infections 660.e1
Toxoplasmosis 660.e1
Sexually Transmitted Diseases 660.e1
Other Disorders 660.e1
37 Pallor and Anemia 661
Introduction 661
History 661
Physical Examination 661
Laboratory Evaluation 662
Classification of Anemia 663
Reticulocyte Count 663
Red Blood Cell Size 663
Red Blood Cell Morphology 664
Other Laboratory Abnormalities Associated with Anemia 665
Diagnostic Work-up 665
Differential Diagnosis of Anemia 667
Anemia Secondary to Acute Blood Loss 667
Anemia Secondary to Underproduction 668
Microcytic Anemias 669
Iron deficiency anemia. 669
Thalassemia syndromes. 670
Lead poisoning. 671
Anemia of inflammation. 671
Rare causes of microcytic anemia. 671
Normocytic Anemia Secondary to Underproduction 671
Macrocytic Anemia (Figs. 37.1 and 37.4) 673
Megaloblastic anemia (vitamin B12 deficiency or folate deficiency). 673
Anemia caused by increased red blood cell destruction. 674
Membrane defects. 674
Enzyme defects. 675
Hemoglobinopathies. 675
Acquired autoimmune hemolytic anemia. 676
Anemia in the Neonate 677
Neonatal Anemia Caused by Blood Loss 677
Neonatal Anemia Caused by Decreased Red Blood Cell Production 678
Neonatal Anemia Caused by Increased Red Blood Cell Destruction 678
Summary and Red Flags 681
References 681
References 681.e1
Work-up of Anemia 681.e1
Anemia with Acute and Chronic Disease 681.e1
Hemolytic Anemia 681.e1
Hypoplastic Anemia 681.e1
Iron Deficiency 681.e1
Macrocytic Anemia 681.e1
38 Bleeding and Thrombosis 682
Coagulation Cascade 682
Coagulation Inhibitors 682
Antithrombin 682
Protein C/Protein S System 682
Fibrinolytic System 682
Platelet-Endothelial Cells Axis 683
Developmental Hemostasis 685
Clues From History and Physical Examination 685
History 685
Physical Examination 685
Coagulation Screening Tests 687
Prothrombin Time and Partial Thromboplastin Time 687
Bleeding Time 688
Platelet Function Analysis 688
Thrombin Time and Reptilase Time 688
Mucocutaneous Bleeding 688
Neonatal Thrombocytopenia 691
Child Abuse 692
Chronic/Insidious Onset of Mucocutaneous Bleeding 692
Platelet Function Defects 693
Chronic Thrombocytopenic Syndromes 693
Deep Bleeding 694
Surgical Bleeding 695
Generalized Bleeding 695
Disseminated Intravascular Coagulation 695
Neonatal Purpura Fulminans 697
Other Causes of Generalized Bleeding 697
Thrombosis 698
Venous Thromboembolic Disease 698
Diagnostic Approach 698
Specific Diagnostic Studies 698
Thrombophilia Testing 698
Arterial Thrombosis 699
Anticoagulant Therapy 699
Heparin 699
Fibrinolytic Therapy 699
Warfarin 700
Summary and Red Flags 700
References 700
References 700.e1
General 700.e1
Coagulopathy 700.e1
Platelets 700.e1
Thrombosis 700.e1
Therapy 700.e1
9 Infectious Diseases 701
39 Fever 701
Pathophysiology of Fever 701
Fever Without Source 701
History 702
Fever: Temperature Measurement 702
Physical Examination 702
Observational Scales 702
Differential Diagnosis 702
Urinary Tract Infections (UTIs) 703
Bacteremia 703
Role of Diagnostic Testing in Patients with Fever Without Source 704
Complete Blood Count and Other Markers of Inflammation 704
Polymerase Chain Reaction (PCR) 704
Blood Cultures 705
Urinalysis and Urine Culture 705
Lumbar Puncture 705
Chest Radiographs 705
Stool Cultures 705
Evaluation and Management 705
Children Younger Than 3 Months 705
Children Aged 3 to 36 Months 706
Children Older Than 36 Months 707
Central Nervous System Infections 707
Bacterial Meningitis 707
Diagnostic Studies 708
Lumbar Puncture and Cerebrospinal Fluid Analysis 708
Computed Tomography 712
Other Laboratory Tests 712
Aseptic Meningitis 712
Viral Meningitis 712
Tuberculous Meningitis 712
Encephalitis 714
Fever of Unknown Origin 714
Evaluation 716
History 716
Physical Examination 719
Eyes 719
Ears, Nose, and Throat 719
Neck 719
Heart, Lungs, and Abdomen 720
Musculoskeletal Evaluation 720
Skin 721
Diagnostic Studies 721
Cause 721
Infections 721
Bacterial endocarditis. 721
Urinary tract infection. 721
Sinusitis. 721
Abscesses. 722
Osteomyelitis. 722
Rheumatic fever. 722
Bacterial Syndromes 722
Lyme disease. 722
Cat-scratch disease. 722
Q fever. 722
Rat bite fever. 722
Tularemia. 722
Brucellosis. 722
Leptospirosis. 722
Fungal Infections 722
Chlamydial Infection 723
Rickettsial Infections 723
Rocky mountain spotted fever. 723
Ehrlichiosis and Anaplasmosis. 723
Viral Infections 723
Cytomegalovirus infection. 723
Infectious mononucleosis. 723
Human immunodeficiency virus infection. 723
Parasites 723
Infections in Children Who Live in or Have Traveled to Developing Countries 723
Malaria 723
Hepatitis 723
Typhoid Fever (Enteric Fever) 723
Tuberculosis 723
Amebiasis 724
Rheumatic Causes of Fever of Unknown Origin 724
Juvenile Idiopathic Arthritis 724
Polyarteritis 724
Systemic Lupus Erythematosus 724
Behçet Syndrome 724
Neoplasms 724
Hodgkin Disease 724
Lymphoma 724
Neuroblastoma 724
Leukemia 724
Pheochromocytoma 724
Miscellaneous Causes of Fever of Unknown Origin 724
Genetic Diseases (See Chapter 41) 724
Drug Fever 724
Kawasaki Disease 724
Inflammatory Bowel Disease 724
Thyrotoxicosis 725
Factitious Disorders 725
Patients in Whom No Diagnosis Is Made 725
Summary and Red Flags 725
References 725
References 725.e1
General 725.e1
Fever Without Source 725.e1
Central Nervous System Infection 725.e1
Fever of Unknown Origin 725.e2
40 Fever and Rash 726
Fever and Rash 726
History 726
Examination 726
Specific Skin Lesions 727
Maculopapular Eruptions 727
Petechiae and Purpura 735
Vesiculobullous Eruptions 735
Nodules 736
Ulcers 736
Erythema 736
Other Physical Examination Findings 736
Joint Manifestations 736
Cardiac Manifestations 737
Ocular Manifestations 737
Neurologic Manifestations 737
Pulmonary Manifestations 737
Clusters of Findings 737
Diagnostic Studies 737
Laboratory Tests 738
Histopathology 738
Other Diagnostic Studies 738
Diagnosis and Decision Making 738
Clinical Syndromes 739
Kawasaki Disease 739
Toxic Shock Syndrome 739
Staphylococcal Toxic Shock Syndrome 739
Streptococcal Toxic Shock Syndrome 740
Erythema Multiforme 742
Stevens–Johnson Syndrome, Toxic Epidermal Necrolysis, and Staphylococcal Scalded Skin Syndrome 742
Serum Sickness and Serum Sickness-Like Reaction 743
Henoch-Schonlein Purpura 744
Other Disorders 744
Management 744
Summary and Red Flags 745
References 745
References 745.e1
41 Recurrent Fever, Infections, Immune Disorders, and Autoinflammatory Diseases 746
History and Physical Examination 746
History 746
Perinatal History 746
Medical History 746
Anatomic Abnormalities 747
Family History 750
Environmental History 750
Physical Examination 750
Diagnostic Categories 751
Patient Who Is Probably Healthy 751
Patient with Hereditary Inflammatory Disorders 751
Immunodeficient Patient 751
Diagnostic Approach to the Patient with Recurrent Infections 751
Humoral Immune Disorders 756
X-Linked Agammaglobulinemia (XLA) 756
Common Variable Immunodeficiency 756
Transient Hypogammaglobulinemia of Infancy 758
Immunoglobulin A Deficiency 758
Specific Antibody Deficiency 758
Hyperimmunoglobulin M Syndrome 758
Combined Immunodeficiency Disorders 759
Severe Combined Immunodeficiency 759
Combined Immune Deficiencies 759
Purine Nucleoside Phosphorylase Deficiency 762
Hyperimmunoglobulin E Syndrome 762
Immunodeficiencies With Syndromic Features 762
Wiskott-Aldrich Syndrome 762
Ataxia-Telangiectasia 762
DiGeorge Syndrome (22q Deletion Syndrome) and Other Thymic Defects 764
Cartilage-Hair Hypoplasia 764
Complement System Deficiencies 764
Diagnosis of Complement Deficiencies 766
Phagocyte Disorders 766
Disorders of Neutrophil Numbers 766
Inherited Forms of Neutropenia 766
Acquired Neutropenia 767
Disorders of Neutrophil Adhesion and Chemotaxis 767
Disorders of Neutrophil Function 767
Disorders of Macrophage Function 769
Asplenia 769
Autoinflammatory Disorders 770
Familial Mediterranean Fever 770
Pyogenic Arthritis, Pyoderma Gangrenosum, and Acne Syndrome 770
Cryopyrin-Associated Periodic Syndromes 770
Hyperimmunoglobulin D Syndrome 771
Deficiency of the Interleukin-1 Receptor Antagonist 771
TNF Receptor–Associated Periodic Syndrome (TRAPS) 771
Deficiency of Adenosine Deaminase 2 771
Blau Syndrome 771
Majeed Syndrome 771
Immune Dysregulation Syndromes 771
Hemophagocytic Lymphohistiocytosis 772
X-Linked Lymphoproliferative Disease Type 1 and Type 2 772
Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked and Related Disorders 772
CD25 Deficiency 772
Signal Transducer and Activator of Transcription Protein 5B Deficiency 772
Cytotoxic T Lymphocyte Antigen 4 Deficiency 772
Autoimmune Polyendocrinopathy-Candidiasis–Ectodermal Dystrophy 772
Autoimmune Lymphoproliferation Syndrome 773
Summary and Red Flags 773
References 773
References 773.e1
Overview, History, Exam, and Diagnostic Approach 773.e1
Complement System Deficiency 773.e1
Phagocyte Disorders 773.e1
Asplenia 773.e1
Humoral Immune Defects 773.e1
Combined Immune Deficiencies 773.e1
Autoinflammatory and Immune Dysregulation Disorders 773.e1
10 Endocrine and Metabolic Disorders 774
42 Disorders of Puberty 774
Normal Pubertal Development 774
Terminology 774
Anatomy 774
Physiology 774
Perinatal Period and Infancy 774
Childhood 774
Adolescence 774
Sex Steroid Effects 775
Chronology of Puberty 775
Females 775
Males 775
Clinical Staging of Puberty 776
Females 776
Males 776
Females and Males 776
Family Patterns 776
Precocious Puberty 776
Definition 776
Normal Variants 776
Idiopathic Isolated Premature Thelarche 776
Idiopathic Isolated Precocious Adrenarche 777
Isosexual Central Precocious Puberty 777
Incomplete Isosexual Precocity (Precocious Pseudopuberty) 778
Androgen Exposure or Overproduction 780
Females. 780
Males. 780
Estrogen Overproduction 780
McCune–Albright syndrome. 781
Vaginal Bleeding 781
Gynecomastia 781
Diagnostic Approach to Precocious Puberty 781
Treatment of Precocious Puberty 783
General Issues 783
Central Precocious Puberty 784
Precocious Pseudopuberty (Incomplete Isosexual Precocity) 784
Delayed or Absent Puberty 784
Differential Diagnosis 784
Constitutional Delay of Growth and Puberty 785
Hypogonadotropic Hypogonadism 786
Kallmann syndrome. 786
Hypergonadotropic Hypogonadism: Males 787
Klinefelter syndrome. 787
Hypergonadotropic Hypogonadism: Females 787
Turner syndrome. 787
Females with Delayed or Absent Adrenarche 787
Diagnostic Approach to Delayed Puberty 787
Treatment of Delayed Puberty 788
Summary and Red Flags 790
References 790
References 790.e1
Normal Pubertal Development 790.e1
Precocious Puberty 790.e1
Delayed or Absent Pubertal Development 790.e1
43 Short Stature 791
Definition 791
Normal Growth 791
Fetal Growth and Birth Size 791
Postnatal Growth Patterns 791
Measuring a Child 793
Body Proportions 793
Familial and Genetic Factors 795
Ethnic Factors and Secular Trend 795
General Well-Being 795
Psychologic Factors 795
Endocrine Regulation of Growth 795
Bone Age 796
Causes of Short Stature 796
Normal Variants 796
Familial Short Stature 796
Constitutional Delay of Growth and Puberty 798
Idiopathic Short Stature 799
Small for Gestational Age 799
Endocrine Disorders 799
Growth Hormone Deficiency 799
Growth Hormone Deficiency Presenting in the Neonatal Period 799
Growth Hormone Deficiency in Childhood 800
Acquired Growth Hormone Deficiency 800
Growth Hormone Insensitivity 801
Hypothyroidism 801
Glucocorticoid Excess (Cushing Syndrome) 803
Other Endocrine Disorders 803
Genetic Causes of Short Stature 803
Turner syndrome. 803
Down syndrome. 804
Prader–Willi syndrome (PWS). 804
Russell–Silver syndrome. 804
Short stature HomeoboX gene mutations. 804
Noonan syndrome. 805
Malnutrition 805
Chronic Illness 805
Emotional Deprivation 806
Iatrogenic Causes 806
Bone Dysplasias 806
Achondroplasia 806
Hypochondroplasia 807
Osteogenesis Imperfecta 807
Evaluating the Child With Short Stature 807
Important Considerations in the History 808
Pregnancy and Birth History 808
Infancy and Childhood 808
Review of Systems 808
Family History 808
Physical Examination 808
Therapeutic Options 808
Specific Treatment of the Primary Disorder 808
Sex Steroids 809
Counseling 809
Growth Hormone Therapy 809
Other Treatments 809
Summary and Red Flags 809
References 810
References 810.e1
44 Hypoglycemia 811
Definition of Hypoglycemia 811
Regulation of Blood Glucose Concentration 811
Clinical Manifestations 813
Causes of Transient Neonatal Hypoglycemia 813
Normal Newborns 813
Newborns Small for Gestational Age and Premature Infants 814
Infants of Diabetic Mothers 814
Perinatal Stress-Induced Hyperinsulinism 814
Erythroblastosis Fetalis 814
Intrapartum Maternal Glucose Administration 814
Maternal Drug Therapy 816
Beckwith-Wiedemann Syndrome 816
Causes of Persistent Hypoglycemia in Infants and Children 816
Hyperinsulinism 816
Recessive KATP Channel Hyperinsulinism 816
Focal KATP Channel Hyperinsulinism 816
Dominant KATP Channel Hyperinsulinism 816
Dominant Glutamate Dehydrogenase Hyperinsulinism 816
Dominant Glucokinase Hyperinsulinism 817
Insulinoma 817
Insulin Reaction, Oral Hypoglycemic Agents, and Surreptitious Insulin Administration 817
Counter-Regulatory Hormone Deficiencies 817
Hypopituitarism 817
Isolated Cortisol Deficiency 819
Epinephrine Deficiency 819
Metabolic Enzyme Defects 819
Hepatic Gluconeogenesis 819
Glucose-6-phosphatase deficiency (Glycogen storage disease type 1a and type 1b). 819
Glucose transporter 2 deficiency (Fanconi-Bickel syndrome). 820
Fructose-1,6-diphosphatase deficiency. 820
Pyruvate carboxylase deficiency. 820
Hepatic Glycogenolysis 820
Debrancher enzyme deficiency (type 3 glycogen storage disease). 820
Phosphorylase/phosphorylase kinase deficiency. 820
Glycogen synthase deficiency. 820
Fatty Acid Oxidation Disorders 820
Other Metabolic Causes of Hypoglycemia 820
Glucose transporter 1 deficiency. 820
Hereditary fructose intolerance. 820
Galactosemia (galactose-1-phosphate uridyl transferase deficiency). 821
Reactive Hypoglycemia 821
Glutamate dehydrogenase-hyperinsulinism, hyperinsulinism/hyperammonemia syndrome. 821
Post–Nissen fundoplication hypoglycemia (late dumping syndrome). 821
Hereditary fructose intolerance. 821
Diagnosis of Hypoglycemia 821
Critical Samples 821
Fasting Study 821
Useful “Casual Specimen” Tests 823
Glucagon Stimulation 823
Acute Insulin Response Tests for Hyperinsulinism 823
Plasma Acyl-Carnitine Profile 823
Urinary Organic Acid Quantitation 823
Cultured Cells 823
Mutation Analysis 823
Treatment of Hypoglycemia 823
Summary and Red Flags 823
References 823
References 823.e1
General 823.e1
Hyperinsulinism 823.e1
Fatty Acid Oxidation Disorders 823.e1
45 Urinary Incontinence and Polyuria 824
Voiding Physiology 824
Toilet Training 824
Urine Volume and Solute Diuresis 824
History 825
Polyuria 825
Voiding History 825
Primary Nocturnal Enuresis 826
Behavioral Issues 826
Physical Examination 826
Diagnosis 826
Laboratory Assessment 827
Imaging and Cystometry 827
Differential Diagnosis 827
Primary Nocturnal Enuresis 827
Dysfunctional Voiding 827
Mild voiding dysfunction. 828
Moderate voiding dysfunction. 828
Severe dysfunctional voiding. 828
Neuropathic Bladder 828
Anatomic Defects 828
Posterior urethral valves and urethral obstruction. 828
Renal duplication. 828
Vesicoureteral reflux. 828
Metabolic Disorders 828
Hypercalcemia. 828
Hypokalemia. 828
Diabetes mellitus. 829
Central Diabetes Insipidus 829
Renal Concentrating Defects 829
Renal tubular acidosis. 829
Sickle cell disease. 829
Nephronophthisis. 829
Nephrogenic diabetes insipidus. 829
Treatment 829
Primary Nocturnal Enuresis 829
Dysfunctional Voiding 830
Polyuria 830
Neuropathic Bladder and Anatomic Disorders 830
Summary and Red Flags 830
References 830
References 830.e1
Voiding Physiology 830.e1
Signs and Symptoms 830.e1
Diagnostics 830.e1
Specific Disorders 830.e1
Treatment 830.e1
46 Acid–Base and Electrolyte Disturbances 831
Acid–Base Balance 831
Acid–Base Disorders 831
Symptoms of Acid–Base Disorders 831
Renal Regulation of Acid–Base Balance 831
Metabolic Acidosis 833
Normal Anion Gap (Hyperchloremic) Metabolic Acidosis 833
Renal Tubular Acidosis 833
Additional Causes of Renal Loss of Bicarbonate 834
Gastrointestinal Loss of Bicarbonate 834
Miscellaneous Causes of Hyperchloremic Acidosis 834
Recovery from ketoacidosis. 834
Dilutional acidosis. 834
Parenteral alimentation. 834
Increased Anion Gap Acidosis 834
Increased Acid Production 834
Diabetic ketoacidosis. 834
Lactic acidosis. 836
Inborn errors of metabolism. 836
Poisonings. 836
Failure of Acid Excretion 836
Treatment of Metabolic Acidosis 836
Metabolic Alkalosis 836
Factors Initiating Metabolic Alkalosis 836
Factors Responsible for Sustaining Alkalosis 836
Differential Diagnosis of Metabolic Alkalosis 837
Urinary Chloride Level Lower Than 15 mEq/L 837
Chloride-deficient diet. 837
Upper gastrointestinal losses. 837
Chloride secreting diarrhea. 837
Diuretic therapy. 837
Hypercapnia. 837
Urinary Chloride Level Higher Than 20 mEq/L with Hypertension 837
Urinary Chloride Level Higher Than 20 mEq/L with Normal Blood Pressure 837
Bartter syndrome and Gitelman syndrome. 837
Treatment of Metabolic Alkalosis 838
Respiratory Acidosis 838
Respiratory Alkalosis 838
Mixed Acid–Base Disorders 839
Potassium Disorders 839
Hypokalemia 839
Increased Renal Losses with Hypertension 839
Mineralocorticoid Excess 839
Liddle Syndrome 839
Increased Renal Losses with Normal Blood Pressure 839
Increased Extrarenal Losses 840
Redistribution 840
Consequences of Hypokalemia 840
Treatment of Hypokalemia 840
Hyperkalemia 841
Reduced Urinary Potassium Excretion 841
Renal Failure 841
Hypoaldosteronism 841
Drugs 841
Primary Tubular Defects 841
Increased Potassium Intake/Tissue Release 841
Redistribution 842
Consequences of Hyperkalemia 842
Treatment of Hyperkalemia 842
Sodium Disorders 842
Hyponatremia 843
Hypovolemic Hyponatremia 843
Euvolemic Hyponatremia 843
Hypervolemic Hyponatremia 843
Clinical Signs and Symptoms of Hyponatremia 844
Treatment of Hyponatremia 844
Hypernatremia 844
Hypovolemic Hypernatremia 844
Euvolemic Hypernatremia 844
Hypervolemic Hypernatremia 846
Clinical Signs and Symptoms of Hypernatremia 846
Treatment of Hypernatremia 846
Calcium Disorders 846
Hypocalcemia 846
Hypercalcemia 846
Rickets 846
Clinical Manifestations 846
Summary and Red Flags 848
References 850
References 850.e1
Acid–Base Disorders 850.e1
Potassium Disorders 850.e1
Sodium Disorders 850.e1
Calcium Disorders 850.e1
Rickets 850.e1
11 Dermatology 851
47 Congenital Cutaneous Lesions and Infantile Rashes 851
Rashes 851
Papules and Pustules—Diffuse or Scattered 851
Patches and Plaques 854
Fixed Lesions 855
Macules, Papules, and Pustules 855
Plaques and Patches 857
Pink (Vascular or Other) 857
Hyperpigmented or Darker Pigmented Lesions 861
Hypopigmented and Depigmented Lesions 862
Other 863
Transient and Physiologic Changes to the Skin 865
Cutis Marmorata 865
Harlequin Color Change 865
Acrocyanosis 865
Summary and Red Flags 865
References 865
References 865.e1
Rashes: Papules and Pustules 865.e1
Rashes: Patches and Plaques 865.e1
Fixed Lesions: Macules, Papules, and Pustules 865.e1
Fixed Lesions: Plaques and Patches 865.e1
Fixed Lesions: Hyperpigmented or Darker Pigment 865.e1
Fixed Lesions: Other 865.e2
Transient and Physiologic Changes of the Skin 865.e2
48 Acquired Rashes in the Older Child 866
History, Physical Examination, and Diagnostic Procedures 866
History 866
Physical Examination 866
Primary Lesions 866
Secondary Lesions 866
Diagnostic Techniques 866
Potassium Hydroxide Test 866
Tzanck Smear 867
Scabies Test 868
Gram Stain 868
Wood Lamp Examination 868
Skin Biopsy 868
Dermatologic Disorders in Older Infants and Children 868
Scaling Disorders 868
Pityriasis Rosea 868
Psoriasis 870
Pityriasis Lichenoides 871
Lichen Planus 871
Seborrheic Dermatitis 872
Atopic Dermatitis 872
Lumps and Bumps 873
Granuloma Annulare 874
Juvenile Xanthogranuloma 875
Vascular Lesions 876
Spider Angioma (Nevus Araneus) 876
Pyogenic Granuloma 878
Disorders of Pigmentation 878
Acquired Disorders of Hypopigmentation or Depigmentation 878
Postinflammatory Hypopigmentation 878
Pityriasis Alba 878
Vitiligo 878
Disorders of Hyperpigmentation 879
Lentigines 879
Café-Au-Lait Macules 879
Postinflammatory Hyperpigmentation 880
Acquired Melanocytic Nevi 880
Melanoma 880
Reactive Erythemas 880
Morbilliform Drug Eruption 880
Fixed Drug Eruption 880
Hypersensitivity Reactions 881
Urticaria 881
Erythema Multiforme 881
Stevens–Johnson Syndrome/Toxic Epidermal Necrolysis Complex 882
Allergic Contact Dermatitis 884
Bullous Lesions 884
Staphylococcal Scalded Skin Syndrome 884
Epidermolysis Bullosa 886
Purpura and Petechiae 887
Henoch–Schönlein Purpura 887
Hair Loss 888
Alopecia Areata 888
Tinea Capitis 889
Traction Alopecia 890
Trichotillomania 890
Telogen Effluvium 890
Infections and Infestations 890
Impetigo 890
Nonbullous Impetigo 890
Bullous Impetigo 890
Molluscum Contagiosum 891
Warts 891
Common Warts 891
Flat Warts 892
Plantar Warts 892
Genital Warts 892
Treatment of Warts 892
Herpes Simplex Virus 892
Varicella 892
Herpes Zoster 893
Scabies 893
Pediculosis 894
Candidiasis 894
Dermatophytoses 895
Tinea Capitis 895
Tinea Corporis 895
Tinea Pedis 895
Tinea Faciei 895
Tinea Cruris 895
Tinea Versicolor 895
Acne Vulgaris 896
Summary and Red Flags 896
References 896
References 896.e1
General Overview 896.e1
Scaling Disorders 896.e1
Lumps and Bumps 896.e1
Disorders of Pigmentation 896.e1
Reactive Erythemas and Hypersensitivity Reactions 896.e1
Bullous Lesions 896.e1
Purpura 896.e1
Hair Loss 896.e1
Infections and Infestations 896.e1
Index 897
A 897
B 900
C 901
D 904
E 906
F 907
G 909
H 910
I 912
J 914
K 914
L 914
M 915
N 917
O 918
P 919
Q 921
R 921
S 923
T 925
U 927
V 927
W 928
X 929
Y 929
Z 929
Inside Back Cover ibc1