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  • MR Neuroimaging: Brain, Spine, Peripheral Nerves
  • Title Page
  • Copyright
  • Contents
  • Preface
  • Contributors
  • Abbreviations
  • Part I Brain
    • 1 Anatomy
      • 1.1 Introduction
      • 1.2 Brain Structures
        • 1.2.1 Cerebrum
        • 1.2.2 Cerebellum
        • 1.2.3 Brainstem
        • 1.2.4 Magnetic Resonance Imaging of Brain Structures
      • 1.3 Brain Surface
        • 1.3.1 Illustrative Cases
          • Case 1
          • Case 2
          • Case 3
          • Case 4
      • 1.4 Sectional Imaging Anatomy
        • 1.4.1 White Matter
        • 1.4.2 Commissures
          • Corpus Callosum
          • Anterior Commissure
          • Posterior Commissure
          • Commissura Habenularum
        • 1.4.3 Deep Gray Matter
        • 1.4.4 Brainstem and Cerebellum
          • Midsagittal Plane
          • Parasagittal Planes
          • Axial Planes
          • Coronal Planes
        • 1.4.5 Cranial Nerves
          • Olfactory Nerves and Olfactory Bulb (Cranial Nerve I)
          • Optic Nerve (Cranial Nerve II)
          • Oculomotor Nerve (Cranial Nerve III)
          • Trochlear Nerve (Cranial Nerve IV)
          • Trigeminal Nerve (Cranial Nerve V)
          • Abducens Nerve (Cranial Nerve VI)
          • Facial Nerve (Cranial Nerve VII)
          • Vestibulocochlear Nerve (Cranial Nerve VIII)
          • Glossopharyngeal Nerve (Cranial Nerve IX)
          • Vagus Nerve (Cranial Nerve X)
          • Accessory Nerve (Cranial Nerve XI)
          • Hypoglossal Nerve (Cranial Nerve XII)
      • 1.5 Variants of Brain Anatomy without Clinical Significance
      • Further Reading
    • 2 Vascular Diseases
      • 2.1 Cerebral Ischemia
        • 2.1.1 Epidemiology
        • 2.1.2 Clinical Manifestations and Treatment
        • 2.1.3 Pathogenesis and Pathophysiology
          • Large-Vessel Disease
          • Small-Vessel Disease
          • Rare Causes of Stroke
        • 2.1.4 MRI Findings
          • Large-Vessel Infarcts
          • Small-Vessel Infarcts
          • Cerebral Amyloid Angiopathy
          • Posterior Reversible Encephalopathy
          • Other Nonatherosclerotic Vascular Diseases
      • 2.2 Intracerebral Hemorrhage
        • 2.2.1 Epidemiology
        • 2.2.2 Clinical Manifestations and Treatment
        • 2.2.3 Pathogenesis and Pathophysiology
        • 2.2.4 MRI Findings
          • Arteriovenous Angiomas
          • Dural Arteriovenous Fistulas
          • Cavernomas
          • Capillary Telangiectasia
          • Developmental Venous Anomaly
      • 2.3 Subarachnoid Hemorrhage
        • 2.3.1 Epidemiology
        • 2.3.2 Clinical Manifestations and Treatment
        • 2.3.3 Pathogenesis and Pathophysiology
        • 2.3.4 MRI Findings
      • 2.4 Cerebral Venous Sinus Thrombosis
        • 2.4.1 Epidemiology
        • 2.4.2 Clinical Manifestations and Treatment
        • 2.4.3 Pathophysiology and Pathogenesis
        • 2.4.4 MRI Findings
      • Further Reading
    • 3 Brain Tumors
      • 3.1 Introduction
      • 3.2 Astrocytic Tumors
        • 3.2.1 Pilocytic Astrocytoma
        • 3.2.2 Pleomorphic Xanthoastrocytoma
        • 3.2.3 Diffuse Astrocytoma
        • 3.2.4 Anaplastic Astrocytoma and Glioblastoma
        • 3.2.5 Gliosarcoma
        • 3.2.6 Gliomatosis Cerebri
      • 3.3 Nonastrocytic Gliomas
        • 3.3.1 Olidodendroglioma and Anaplastic Olidodendroglioma
        • 3.3.2 Oligoastrocytic Tumor
        • 3.3.3 Ependymoma
        • 3.3.4 Subependymoma
        • 3.3.5 Anaplastic Ependymoma
      • 3.4 Neuroepithelial Tumors
        • 3.4.1 Gangliocytoma and Ganglioglioma
        • 3.4.2 Desmoplastic Infantile Ganglioglioma
        • 3.4.3 Central Neurocytoma
        • 3.4.4 Dysembryoplastic Neuroepithelial Tumor
        • 3.4.5 Dysplastic Cerebellar Gangliocytoma (Lhermitte–Duclos Disease)
        • 3.4.6 Hypothalamic/Tuber Cinereum Hamartoma
      • 3.5 Embryonal Tumors
        • 3.5.1 Medulloblastoma
        • 3.5.2 Supratentorial Primitive Neuroectodermal Tumor
      • 3.6 Meningeal Tumors
        • 3.6.1 Meningioma
        • 3.6.2 Nonmeningeal Mesenchymal Tumors
        • 3.6.3 Hemangiopericytoma
        • 3.6.4 Primary Melanocytic Lesion
      • 3.7 Pineal Tumors
        • 3.7.1 Pineoblastoma
        • 3.7.2 Pineocytoma
        • 3.7.3 Pineal Cyst
        • 3.7.4 Germinoma
        • 3.7.5 Pineal Teratoma
      • 3.8 Tumors of the Sellar Region
        • 3.8.1 Pituitary Adenoma
        • 3.8.2 Craniopharyngioma
        • 3.8.3 Dysontogenetic Lesions
          • Pars Intermedia and Colloid Cysts
          • Rathke Cleft Cyst
          • Epidermoid
          • Dermoid
          • Ectopic Neurohypophysis
        • 3.8.4 Germinoma
        • 3.8.5 Chordoma and Chondroma
          • Chordoma
          • Chondroma
        • 3.8.6 Optic Nerve Glioma
        • 3.8.7 Paraganglioma
        • 3.8.8 Infundibular Tumor
      • 3.9 Metastases
        • 3.9.1 Meningeal Metastases
          • Dural Metastases
          • Leptomeningeal Metastases
        • 3.9.2 Parenchymal Metastases
      • 3.10 Miscellaneous Tumors
        • 3.10.1 Primary Cerebral Lymphoma
        • 3.10.2 Choroid Plexus Tumors (Choroid Plexus Papilloma and Carcinoma)
          • Choroid Plexus Cyst
          • Xanthogranulomas
        • 3.10.3 Choroid Plexus Papilloma
        • 3.10.4 Hemangioblastoma
        • 3.10.5 Peripheral Nerve Sheath Tumor
          • Schwannoma
          • Neurofibroma
          • Neurofibrosarcoma
        • 3.10.6 Esthesioneuroblastoma
      • 3.11 Nonneoplastic Cysts and Tumorlike Lesions
        • 3.11.1 Arachnoid Cyst
        • 3.11.2 Neuroepithelial Cyst
        • 3.11.3 Colloid Cyst
        • 3.11.4 Epidermoid
        • 3.11.5 Dermoid
        • 3.11.6 Lipoma
      • Further Reading
    • 4 HeadTrauma
      • 4.1 Introduction and Epidemiology
      • 4.2 Classification and Clinical Grading
      • 4.3 Magnetic Resonance Imaging of Head Trauma
        • 4.3.1 Role of MRI in Trauma Diagnosis
        • 4.3.2 Examination Technique
        • 4.3.3 MRI Detection of Intracranial Hemorrhage
        • 4.3.4 Prognostic Value of MRI
      • 4.4 Primary Traumatic Lesions
        • 4.4.1 Skull Fractures
        • 4.4.2 Epidural Hematoma
          • Acute Epidural Hematoma
          • Chronic Epidural Hematoma
        • 4.4.3 Subdural Hematoma
          • Acute Subdural Hematoma
          • Chronic Subdural Hematoma
        • 4.4.4 Subdural Hygroma
        • 4.4.5 Traumatic Subarachnoid Hemorrhage
        • 4.4.6 Intraventricular Hemorrhage
        • 4.4.7 Cranial Nerve Injuries
        • 4.4.8 Brain Contusions
        • 4.4.9 Shearing Injuries (Diffuse Axonal Injury)
        • 4.4.10 Intracerebral Hematomas
        • 4.4.11 Traumatic Lesions of the Brainstem and Basal Ganglia
        • 4.4.12 Primary Vascular Lesions
      • 4.5 Secondary Traumatic Lesions
        • 4.5.1 Brain Edema
        • 4.5.2 Herniation Syndromes
          • Subfalcine Herniation
          • Descending Transtentorial Herniation
          • Ascending Transtentorial Herniation
          • Tonsillar Herniation
        • 4.5.3 Secondary Brainstem Lesions
        • 4.5.4 Brain Death
        • 4.5.5 Secondary Vascular Lesions
          • Transfalcial Herniation
          • Descending Transtentorial Herniation
          • Combined Subfalcine and Transtentorial Herniation
        • 4.5.6 Infection
        • 4.5.7 Growing Fracture
        • 4.5.8 Chronic Changes After Head Trauma
      • Further Reading
    • 5 Infections
      • 5.1 Infectious Diseases of the Meninges
      • 5.2 Infectious Diseases of the Brain Parenchyma
        • 5.2.1 Viral Encephalitis
          • Herpes Simplex Viral Encephalitis
          • Cytomegalovirus Encephalitis
          • Epstein–Barr Virus Encephalitis
          • Varicella Zoster Virus Encephalitis
          • Progressive Multifocal Leukoencephalopathy
          • Congenital Rubella Encephalitis
          • Tick-Borne Encephalitis
          • Rabies Encephalitis
          • Measles
          • HIV Encephalitis and Encephalopathy
          • Other, Less Common Viral Encephalitides
          • Differential Diagnosis
        • 5.2.2 Bacterial Infections
          • Pyogenic Cerebritis and Bacterial Brain Abscess
          • Neurotuberculosis
          • Lyme Disease
          • Neurosyphilis
          • Listeriosis
          • Whipple's Disease
        • 5.2.3 Parasitic Brain Diseases
          • Toxoplasmosis
          • Neurocysticercosis
          • Paragonimiasis
          • Echinococcosis
          • Amebiasis
          • Sparganosis
        • 5.2.4 Fungal Infections
          • Aspergillosis
          • Candidiasis
          • Mucormycosis
          • Histoplasmosis
          • Coccidioidomycosis
          • Cryptococcosis
        • 5.2.5 Rickettsioses
        • 5.2.6 Transmissible Spongiform Encephalopathies (Creutzfeldt–Jakob Disease)
      • 5.3 Special Aspects of Postnatal (Congenital) Infections
        • 5.3.1 Infectious Meningitis
          • Neonates
          • Infants and Small Children
        • 5.3.2 Tuberculous Meningitis
        • 5.3.3 Brain Abscess
        • 5.3.4 Encephalitis in Children
        • 5.3.5 Less Common Pediatric Encephalitides
        • 5.3.6 Fungal Diseases in Children
      • Further Reading
    • 6 Multiple Sclerosis and Related Diseases
      • 6.1 Introduction
      • 6.2 Epidemiology
      • 6.3 Clinical Manifestations and Treatment
        • 6.3.1 Clinical Course
          • Categories
        • 6.3.2 Diagnosis
        • 6.3.3 Treatment and Response
      • 6.4 Pathology
      • 6.5 Magnetic Resonance Imaging
        • 6.5.1 Examination Technique
          • Conventional Magnetic Resonance Imaging
          • New Techniques
        • 6.5.2 MRI Findings
          • Primary Demyelinating Diseases
          • Diseases with Secondary Demyelination or Destruction of White Matter
      • 6.6 Differential Diagnosis
      • Further Reading
    • 7 Metabolic Disorders
      • 7.1 Introduction
      • 7.2 Magnetic Resonance Imaging in Metabolic Brain Disorders
        • 7.2.1 Diffusion-WeightedMRI
        • 7.2.2 Magnetic Resonance Spectroscopy
      • 7.3 Normal Myelination in Children
      • 7.4 Metabolic Disorders Primarily Affecting the White Matter
        • 7.4.1 Leukodystrophies Primarily Affecting the DeepWhite Matter
          • Adrenoleukodystrophy
          • Metachromatic Leukodystrophy
          • Krabbe's Disease (Globoid Cell Leukodystrophy)
          • Merosin-Deficient Congenital Muscular Dystrophy
          • Homocystinuria (Hyperhomocysteinemia)
          • Maple Syrup Disease
          • Phenylketonuria
          • Lowe's Syndrome
        • 7.4.2 Leukodystrophies Primarily Affecting the White Matter
          • Megalencephalic Leukoencephalopathy with Subcortical Cysts (Van der Knaap's Disease)
          • Alexander's Disease
          • Cockayne's Syndrome
          • Canavan's Disease
          • Vanishing White Matter Disease (Leukoencephalopathy with Vanishing White Matter)
          • Galactosemia
        • 7.4.3 Hypomyelination Syndromes
          • Pelizaeus–Merzbacher Disease
          • Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum
          • Hypomyelination with Congenital Cataract
          • Hypomyelinating Leukodystrophy with Hypodontia and Hypogonadotropic Hypogonadism
      • 7.5 Metabolic Disorders Primarily Affecting the Gray Matter
        • 7.5.1 Huntington's Disease (Huntington's Chorea)
        • 7.5.2 Sydenham's Chorea (Chorea Minor)
        • 7.5.3 Neurodegeneration with Brain Iron Accumulation
          • Pantothenate Kinase-Associated Neurodegeneration
          • Infantile Neuroaxonal Dystrophy
        • 7.5.4 Neuronal Ceroid Lipofuscinosis
        • 7.5.5 Creatine Metabolism Disorders
        • 7.5.6 Aicardi–Goutieres Syndrome
        • 7.5.7 Niemann–Pick Disease
        • 7.5.8 Rett's Syndrome
        • 7.5.9 Fucosidosis
      • 7.6 Metabolic Diseases of the White and Gray Matter
        • 7.6.1 Wilson's Disease
        • 7.6.2 Mitochondrial Encephalomyelopathy with Lactic Acidosis and Stroke (MELAS)
        • 7.6.3 Myoclonic Epilepsy with Ragged Red Fibers (MERRF)
        • 7.6.4 Leigh's Disease
        • 7.6.5 Glutaric Aciduria
          • Glutaric Aciduria Type 1
          • Glutaric Aciduria Type 2
        • 7.6.6 Kearns–Sayre Syndrome
        • 7.6.7 Zellweger's Syndrome
        • 7.6.8 GM1 and GM2 Gangliosidosis
      • Further Reading
    • 8 Degenerative Diseases
      • 8.1 Introduction
      • 8.2 Magnetic Resonance Imaging
      • 8.3 Neurodegenerative Diseases of the Central Motor System
        • 8.3.1 Wallerian Degeneration
        • 8.3.2 Hypertrophic Olivary Degeneration
        • 8.3.3 Amyotrophic Lateral Sclerosis
        • 8.3.4 Huntington's Disease
        • 8.3.5 Fahr's Disease (Calcification of the Basal Ganglia)
        • 8.3.6 Friedreich's Ataxia
      • 8.4 Parkinson's Disease and Atypical Parkinsonian Syndromes
        • 8.4.1 Parkinson's Disease
        • 8.4.2 Multiple System Atrophy
        • 8.4.3 Corticobasal Degeneration
        • 8.4.4 Progressive Supranuclear Palsy
      • 8.5 Neurodegenerative Forms of Dementia
        • 8.5.1 Alzheimer's Disease
        • 8.5.2 Lewy Body Dementia
        • 8.5.3 Frontotemporal Dementia
      • Further Reading
    • 9 Malformations and Developmental Abnormalities
      • 9.1 Embryology
      • 9.2 Abnormalities of Cortical Development
        • 9.2.1 Group I Malformations
          • Microcephaly and Microcephaly with a Simplified Gyral Pattern
          • Megalencephalies (Group I.B) and Hemimegalencephalies
          • Focal Cortical Dysplasias Type II (Group I.C)
        • 9.2.2 Group II Malformations
          • Periventricular (Subependymal) Heterotopias (Group II.A) and Focal Subcortical Heterotopias (Group II.C)
          • Lissencephalies (Group II.B)
          • Cobblestone Malformations (Group II.D)
        • 9.2.3 Group III Disorders
          • Polymicrogyria and Schizencephaly (Group III.A) and Polymicrogyria without Schizencephaly (Group III.B)
          • Focal Cortical Dysplasia Types I and III (Group III.C)
      • 9.3 Malformations of the Corpus Callosum and Commissures
        • 9.3.1 Malformations and Syndromes Associated with Agenesis of the Corpus Callosum
        • 9.3.2 Intracranial Lipomas with Corpus CallosumAgenesis
        • 9.3.3 Interhemispheric Cysts with Corpus CallosumAgenesis
      • 9.4 Holoprosencephaly
        • 9.4.1 Alobar Holoprosencephaly
        • 9.4.2 Semilobar Holoprosencephaly
        • 9.4.3 Lobar Holoprosencephaly
        • 9.4.4 Septo-optic Dysplasia
        • 9.4.5 Arhinencephaly
      • 9.5 Encephaloceles
        • 9.5.1 Occipital Encephaloceles
        • 9.5.2 Frontoethmoidal Encephaloceles
        • 9.5.3 Nasopharyngeal Encephaloceles
        • 9.5.4 Atretic Cephaloceles
      • 9.6 Chiari Malformations
        • 9.6.1 Chiari Malformation Type I
        • 9.6.2 Chiari Malformation Type II
      • 9.7 Dandy–Walker Malformation
        • 9.7.1 Classic Dandy–Walker Malformation
        • 9.7.2 Hypoplastic Vermis with Rotation
        • 9.7.3 Blake Pouch Cyst
        • 9.7.4 Mega Cisterna Magna
      • 9.8 Hypogenesis, Atrophy, and Dysplasia of the Cerebellum
      • 9.9 Rhombencephalosynapsis
      • 9.10 Lhermitte–Duclos Syndrome
      • 9.11 Joubert's Syndrome and Molar Tooth Malformations
      • 9.12 Neurocutaneous Syndromes
        • 9.12.1 Tuberous Sclerosis
        • 9.12.2 Neurofibromatosis
          • Neurofibromatosis Type 1 (von Recklinghausen's Disease)
          • Neurofibromatosis Type 2
        • 9.12.3 Sturge–Weber Disease
        • 9.12.4 Von Hippel–Lindau Disease
        • 9.12.5 Rare Phacomatoses
      • Further Reading
    • 10 Hydrocephalus and Intracranial Hypotension
      • 10.1 Brief Historical Review
      • 10.2 Fundamentals of Anatomy and Physiology
        • 10.2.1 Functions of the CSF
        • 10.2.2 Anatomy of the CSF Spaces
        • 10.2.3 Production and Transport of CSF
        • 10.2.4 CSF Equilibrium and Hydrocephalus
        • 10.2.5 CSF and Intracranial Hypotension
      • 10.3 Epidemiology
      • 10.4 Imaging
        • 10.4.1 Modalities
          • Computed Tomography
          • Magnetic Resonance Imaging
        • 10.4.2 Imaging Findings
          • General Findings
          • Congenital Hydrocephalus
          • Hypersecretory Hydrocephalus
          • Obstructive Hydrocephalus
          • Malresorptive Hydrocephalus
          • Normal-Pressure Hydrocephalus
          • Intracranial Hypotension
      • Further Reading
  • Part II Spinal Cord
    • 11 Anatomy
      • 11.1 Examination Technique
        • 11.1.1 Imaging Planes in MRI
        • 11.1.2 MRI Sequences
        • 11.1.3 Contrast Agents
      • 11.2 Spinal Column
        • 11.2.1 Vertebrae
          • Cervical Vertebrae
          • Thoracic Vertebrae
          • Lumbar Vertebrae
          • MRI Signal Characteristics of the Vertebral Bodies
        • 11.2.2 Intervertebral Disks
        • 11.2.3 Ligaments
        • 11.2.4 Normal Variants and Malformations
      • 11.3 Spinal Meninges and Intraspinal Compartments
        • 11.3.1 Epidural Space
        • 11.3.2 Subdural Space
        • 11.3.3 Subarachnoid Space
      • 11.4 Spinal CSF Circulation
        • 11.4.1 Subarachnoid Space
        • 11.4.2 Central Canal
      • 11.5 Spinal Cord and Spinal Nerves
        • 11.5.1 Anatomy
        • 11.5.2 Normal Variants
        • 11.5.3 Internal Structure of the Spinal Cord
          • Gray Matter
          • White Matter
      • 11.6 Blood Supply to the Spinal Cord
      • Further Reading
    • 12 Degenerative Spinal and Foraminal Stenoses
      • 12.1 Introduction
      • 12.2 Disk Herniations
        • 12.2.1 Lumbar Disk Herniations
        • 12.2.2 Thoracic Disk Herniations
        • 12.2.3 Cervical Disk Herniations
        • 12.2.4 Postoperative Findings and Complications
          • Recurrent Disk Herniation and Epidural Scarring
          • Postoperative Pseudomeningocele
          • Postoperative Metal Artifacts in MRI
          • Spondylosis Deformans
      • 12.3 Spinal Stenosis
      • Further Reading
    • 13 Trauma
      • 13.1 Introduction
      • 13.2 Examination Technique
      • 13.3 Spinal Ligament Injuries
        • 13.3.1 Injuries of the Craniocervical Junction and Upper Cervical Spine
          • Atlanto-Occipital Dislocation and Subluxation
          • Fractures of the Atlas and Axis
          • Neural Arch Fractures of the Axis
          • Dissection of Arteries Supplying the Brain
        • 13.3.2 Injuries of the Lower Cervical Spine, Thoracic Spine, and Lumbar Spine
          • Classification and Stability of Fractures
          • Determining the Level of a Fracture
          • Age and Etiology of a Fracture
        • 13.3.3 Postoperative Examinations and Follow-Ups
      • 13.4 Spinal Cord Injuries
        • 13.4.1 Acute Spinal Cord Injuries
          • Spinal Cord Contusions
          • Narrowing of the Spinal Canal
          • Posttraumatic Spinal Hemorrhage
          • Stabbing and Gunshot Injuries
        • 13.4.2 Chronic Posttraumatic Spinal Cord Changes
          • Syringohydromyelia and Cysts
          • Transection, Atrophy, Malacia, and Tethering of the Spinal Cord
        • 13.4.3 Nerve Root Injuries
      • Further Reading
    • 14 Tumors and Tumorlike Masses
      • 14.1 Introduction
      • 14.2 Extradural Space
        • 14.2.1 Benign Tumors
          • Hemangioma
          • Giant Cell Tumor
          • Osteochondroma and Cartilaginous Exostosis
          • Chondroblastoma
          • Aneurysmal Bone Cyst
          • Eosinophilic Granuloma
          • Epidural Lipomatosis
          • Extradural Arachnoid Cyst
        • 14.2.2 Malignant Tumors
          • Metastases
          • Multiple Myeloma and Plasmacytoma
          • Lymphoma
          • Chordoma
          • Sarcomas
          • Paraspinal Tumors with Extension into the Spinal Canal
      • 14.3 Intradural Extramedullary Space
        • 14.3.1 Nerve Sheath Tumor
        • 14.3.2 Meningioma
        • 14.3.3 Paraganglioma
        • 14.3.4 Arachnoid Cyst
        • 14.3.5 Cavernoma and Capillary Hemangioma
        • 14.3.6 Metastases and Leptomeningeal Carcinomatosis
          • Metastases
          • Leptomeningeal Carcinomatosis
      • 14.4 Intramedullary Space
        • 14.4.1 Benign Masses
          • Hydrosyringomyelia
          • Hemangioblastoma
          • Intramedullary Neurinoma
          • Cavernous Hemangioma
          • Teratoma
          • Lipoma
          • Postirradiation Changes
        • 14.4.2 Malignant Masses
          • Ependymoma
          • Astrocytoma
          • Ganglioglioma
          • Primitive Neuroectodermal Tumor
          • Atypical Teratoid and Rhabdoid Tumors
          • Germinoma
          • Melanoma
          • Other Tumors
          • Metastases
      • 14.5 Management of Intradural Masses
      • 14.6 Mimics of Spinal Tumors
        • 14.6.1 Intraosseous Disk Herniation
        • 14.6.2 Sequestered Disk
        • 14.6.3 CSF Pulsation Artifact
        • 14.6.4 Spinal Fistulas
        • 14.6.5 Epidural Hematoma
      • Further Reading
    • 15 Vascular Diseases
      • 15.1 Spinal Arterial Ischemia
      • 15.2 Spinal Hemorrhage
        • 15.2.1 Epidural Spinal Hemorrhage
        • 15.2.2 Subdural (Epiarachnoid) Spinal Hemorrhage
        • 15.2.3 Subarachnoid Spinal Hemorrhage
        • 15.2.4 Intramedullary Hemorrhage
        • 15.2.5 Superficial Siderosis of the Central Nervous System
      • 15.3 Cavernous Hemangioma (Cavernoma)
      • 15.4 Spinal Vascular Malformations with Arteriovenous Shunting
        • 15.4.1 Type 1: Spinal Dural Arteriovenous Fistula
        • 15.4.2 Spinal Arteriovenous Malformations Types 2 to 4
      • Further Reading
    • 16 Inflammations, Infections, and Related Diseases
      • 16.1 Introduction
      • 16.2 Intramedullary Space
        • 16.2.1 Multiple Sclerosis and Other Demyelinating Diseases
          • Multiple Sclerosis
          • Acute Disseminated Encephalomyelitis
          • Neuromyelitis Optica (Devic's Syndrome)
        • 16.2.2 Acute Transverse Myelitis
        • 16.2.3 Radiation Myelopathy
        • 16.2.4 Important Differential Diagnoses
          • Spinal Dural Arteriovenous Fistula
          • Funicular Myelosis (Vitamin B12 Deficiency)
      • 16.3 Intradural Extramedullary Space
        • 16.3.1 Meningitis
        • 16.3.2 Guillain–Barré Syndrome
        • 16.3.3 Sarcoidosis
      • 16.4 Extradural Space
        • 16.4.1 Spondylitis, Spondylodiskitis, Spondyloarthritis
        • 16.4.2 Epidural Abscess
      • Further Reading
    • 17 Malformations and Developmental Abnormalities
      • 17.1 Introduction
      • 17.2 Embryology
        • 17.2.1 Gastrulation
        • 17.2.2 Primary Neurulation
        • 17.2.3 Secondary Neurulation and Retrogressive Differentiation
      • 17.3 Classification
      • 17.4 Open Spinal Dysraphisms
        • 17.4.1 Myeloceles and Myelomeningoceles
        • 17.4.2 Hemimyeloceles and Hemimyelomeningoceles
        • 17.4.3 Postoperative Complications
      • 17.5 Closed Spinal Dysraphisms
        • 17.5.1 Closed Spinal Dysraphisms with Subcutaneous Swelling
          • Lipomyeloceles and Lipomyelomeningoceles
          • Myelocystoceles
          • Meningoceles
          • Sacrococcygeal Teratoma
        • 17.5.2 Closed Spinal Dysraphisms with Cutaneous Stigmata
          • Dermal Sinus
          • Dorsal–Enteric Fistula
          • Diastematomyelias
        • 17.5.3 Closed Spinal Dysraphisms without Cutaneous Stigmata
          • Simple Vertebral Arch Defects
          • Segmentation Disorders of the Spinal Column
          • Tight Filum Terminale
          • Lipomas of the Filum Terminale
          • Intradural Lipomas
          • Dermoids and Epidermoids
          • Enterogenous Cysts
          • Caudal Regression Syndrome
          • Segmental Spinal Dysgenesis
          • Anterior Sacral Meningocele
      • Further Reading
  • Part III Peripheral Nervous System
    • 18 Diseases of the Peripheral Nervous System
      • 18.1 Introduction
      • 18.2 Basic Technical Principles of Magnetic Resonance Neurography
      • 18.3 Pathologic Conditions
        • 18.3.1 Traumatic Neuropathies
        • 18.3.2 Nerve Compression Syndromes
        • 18.3.3 Inflammatory Neuropathies
        • 18.3.4 Neoplasms of Peripheral Nerves
        • 18.3.5 Polyneuropathies
      • 18.4 MRI of the Muscles in Neurogenic Muscle Diseases
      • 18.5 Summary
      • Further Reading
  • Index

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