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Welcome to the new AJNR, Updated Hall of Fame, and more. Read the full announcements.


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Case of the Week Diagnoses

Section Editors: Matylda Machnowska1 and Anvita Pauranik2
1University of Toronto, Toronto, Ontario, Canada
2University of British Columbia, Vancouver, British Columbia, Canada

View the archive by date
  • A
  • B
  • C
  • D
  • E
  • F
  • G
  • H
  • I
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  • K
  • L
  • M
  • N
  • O
  • P
  • Q
  • R
  • S
  • T
  • U
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  • W
  • X
  • Y
  • Z
  • All
  • IgG4-related Pachymeningitis
  • "Polio-like" Myelitis
  • "White" Dermoid

1

  • 18q Deletion Syndrome

A

  • A Rare Presentation of Klippel-Feil Syndrome: The Single Cervical Vertebra
  • A von Hippel-Lindau Disease-Associated Primary Clear Cell Microcystic Adenoma in the Sinonasal Cavity
  • Aberrant Internal Carotid Artery
  • Absence of the Left Meckel Cave with Trigeminal Neuropathy
  • Acquired Cholesteatoma of the External Auditory Canal
  • Acquired Epidermoid Cyst
  • Acquired Middle Ear Cholesteatoma
  • ACTA2-related Cerebrovascular Disease
  • Acute Cerebellitis
  • Acute Cerebral Fat Embolism
  • Acute Cerebral Fat Embolism
  • Acute Hemorrhagic Encephalomyelitis (AHEM) Mimicking Abscess
  • Acute Hemorrhagic Leukoencephalitis (AHLE)
  • Acute Hemorrhagic Leukoencephalitis (AHLE) Associated with Leptospirosis
  • Acute Hyperammonemic Encephalopathy
  • Acute Hyperammonemic Encephalopathy
  • Acute Hyperextension “Surfer’s” Myelopathy
  • Acute Idiopathic Carotidynia
  • Acute Ischemia of the Mammillary Bodies
  • Acute Kernicterus (Bilirubin Encephalopathy)
  • Acute Lenticulostriate Artery Infarct with Branch Atheromatous Disease (BAD)
  • Acute Methanol Intoxication
  • Acute Methotrexate Toxicity
  • Acute Methotrexate-Induced Encephalopathy
  • Acute Necrotizing Encephalopathy (ANE) Triggered by Influenza
  • Acute Necrotizing Encephalopathy (ANE)
  • Acute Necrotizing Encephalopathy of Childhood (ANEC)
  • Acute parenchymal neuro-Behçet’s disease
  • Acute Polyradiculoneuropathy in SLE
  • Acute Post-traumatic Spinal Subarachnoid Hematoma
  • Acute Retroclival Subdural Hematoma Secondary to Pituitary Apoplexy
  • Acute Toxic Leukoencephalopathy
  • Adenoid Cystic Carcinoma with Perineural Spread
  • Adrenoleukodystrophy (ALD)
  • Adrenomyeloneuropathy
  • Adult Epiglottitis
  • Adult Mitochondrial Encephalomyopathy: Diabetes Mellitus and Deafness
  • Agenesis of Corpus Callosum
  • Agenesis of the Internal Carotid Artery
  • Agenesis of the Internal Carotid Artery
  • Agenesis of the Internal Carotid Artery
  • Aggressive Spinal Hemangioma
  • Aicardi Syndrome
  • Aicardi-Goutières Syndrome
  • Aicardi-Goutières Syndrome
  • Alexander Disease Type I
  • Allergic Fungal Rhinosinusitis with Intracranial Extension
  • ALVEOLAR PARAMENINGEAL RHABDOMYOSARCOMA
  • Alzheimer-like Dementia in Down's Syndrome
  • Ameloblastic Carcinoma (AC)
  • Ameloblastic fibro-odontoma (AFO)
  • Ameloblastoma
  • Amyloid-Beta–related Angiitis (ABRA)
  • Amyloidosis with Intracerebral Acute Hemorrhage and Superficial Siderosis
  • Amyotrophic Lateral Sclerosis
  • Amyotrophic Lateral Sclerosis (ALS)
  • Anaplastic Neuroepithelial Tumor
  • Anaplastic Oligodendroglioma
  • Ancient Schwannoma
  • Aneurysmal Bone Cyst (ABC) of the Lumbar Spine
  • Aneurysmal Bone Cyst of Temporal Bone
  • Ankylosing Spondylitis + Acute Fracture
  • Anterior Cranial Fossa Dural Arteriovenous Fistula Presenting as Subdural Hematoma
  • Anterior Inferior Cerebellar Artery–Neurovascular Conflict (AICA–NVC) Causing Pulsatile Tinnitus
  • Anterior Sacral Meningocele Related to Marfan Syndrome
  • Anterior Spinal Artery Aneurysm
  • Anterior Spinal Artery Syndrome
  • Anti-Ma2 Antibody Paraneoplastic Encephalitis (Secondary to Mediastinal Seminoma)
  • Anti-NMDA Encephalitis
  • ANTI-NMDA RECEPTOR ENCEPHALITIS
  • Apical Petrositis
  • Arachnoid Cyst with Accessory Nerve Palsy
  • Arachnoid Cyst with Intracystic and Subdural Hematoma
  • Arachnoiditis Ossificans
  • Arterial displasia in PHACE SYNDROME
  • ASL Hypoperfusion Artifacts after Carotid Stenting
  • Aspergillus Fumigatus Cerebral Abscess
  • Astroblastoma
  • Atlanto-Occipital Dislocation (AOD)
  • Atretic Parietal Cephalocele
  • Atretic Parietal Meningocele
  • Atypical Dermoid Cyst
  • Atypical PRES with Spinal Cord Involvement
  • Atypical Posterior Reversible Encephalopathy Syndrome with Spinal Cord Involvement (PRES-SCI)
  • Atypical Vascular Neoplasm of the Cavernous Sinus (Low-to-Intermediate Grade)
  • Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
  • Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS)

B

  • Baastrup Syndrome
  • Balò's Concentric Sclerosis
  • Balo’s Concentric Sclerosis
  • Band Heterotopia
  • Basal Encephalocele and Morning Glory Syndrome
  • Basal Ganglia Stroke in Child Following Mild Head Trauma
  • Basal Meningitis with Isolated Unilateral Basal Vein of Rosenthal Thrombosis
  • Benign Lymphoepithelial Cysts
  • Benign Notochordal Cell Tumor
  • Benign Notochordal Cell Tumor
  • Beta-Propeller Protein-Associated Neurodegeneration (BPAN)
  • Beta-Propeller Protein-Associated Neurodegeneration (BPAN)
  • Bilateral Dacryops
  • Bilateral Dilated Endolymphatic Sacs with Dysplastic Cochleas and Vestibules
  • Bilateral Hypertrophic Olivary Degeneration
  • Bilateral Optic Perineuritis
  • Bilateral Petrous Apex Cephaloceles
  • Bilateral Petrous Apex Cephaloceles (PACs)
  • Bilateral Symmetric Caudate Head Hemorrhage
  • Bilateral Temporal Langerhans Cell Histiocytosis
  • Bilateral Thalamic Infarctions Due to Occlusion of the Paramedian Artery
  • Bing-Neel syndrome (BNS)
  • Bisphosphonate-Associated Osteonecrosis of the Jaws
  • Blunt Cerebrovascular Injury – Denver Grade III (Pseudoaneurysm)
  • Bone Flap Osteomyelitis with Subperiosteal Abscess
  • Brachial Plexitis
  • Brain Abscess (Caused by Prototheca)
  • Brain Calcification in Systemic Lupus Erythematosus (SLE)
  • Brain Death
  • Brain-in-Brain Malformation
  • Brainstem Astrocytoma
  • Brainstem PRES
  • Branchio-Oto-Renal Syndrome
  • Breast Metastasis to the Pineal Gland
  • Brown Tumor of Hyperparathyroidism
  • Bulbar and Spinal Cord Marburg Disease
  • Burkitt's Lymphoma (Endemic Form)

C

  • CADASIL
  • CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy)
  • Calcifying Pseudoneoplasm of the Neural Axis (CAPNON)
  • Calcifying Pseudoneoplasm on the Neuroaxis (CAPNON)
  • Calcinosis Cutis Circumscripta
  • Calvarial plasmacytoma as an initial presentation for multiple myeloma
  • Camurati-Engelmann Disease
  • Canavan Disease
  • Candida Microabscess
  • Capecitabine-Induced Acute Toxic Leukoencephalopathy
  • Capillary Telangiectasia
  • Carcinoma ex pleomorphic adenoma (CXPA) of the orbit arising from the lacrimal gland
  • Carotid Body Tumor (CBT)
  • Carotid Cavernous Sinus Dural Fistula
  • Carotid Web and Ischemic Stroke
  • Carotid-Cochlea Dehiscence
  • Carotidynia or Transient Perivascular Inflammation of the Carotid Artery (TIPIC) Syndrome
  • Cat Scratch Disease
  • Cauda Equina Paraganglioma
  • Caudal Regression Syndrome
  • Cavernous Hemangioma of the Skull
  • Cavernous Sinus Hemangioma
  • Cellular Ependymoma—Cervical Cord
  • Central Giant Cell Granuloma of the Mandible
  • Central Nervous System Tuberculosis Immune Reconstitution Inflammatory Syndrome
  • Central Neurocytoma
  • Central Neurocytoma
  • Central-Variant Posterior Reversible Encephalopathy Syndrome (PRES)
  • Cerebal Coenurosis
  • Cerebellar Dural Arteriovenous Fistula
  • Cerebellar Tumefactive Perivascular Space
  • Cerebral Amyloid Angiopathy (CAA) Associated with Inflammation (Inflammatory CAA)
  • Cerebral Amyloid Angiopathy-Related Inflammation
  • Cerebral Amyloid Angiopathy-related Inflammation (CAA-I)
  • Cerebral Amyloidoma Associated with B-Cell Non-Hodgkin Lymphoma
  • Cerebral Chagas Disease (Chagoma) in a Patient with Previously Unknown AIDS
  • Cerebral Fat Emboli
  • Cerebral Fat Embolism (with Associated Shear Injury)
  • Cerebral Hydatidosis
  • Cerebral Hyperperfusion Syndrome
  • Cerebral Inflammatory Pseudotumor or Plasma cell Granuloma
  • Cerebral Malaria
  • Cerebral Nocardiosis
  • Cerebral (Venous) Air Embolism
  • Cerebrofacial Arteriovenous Metameric Syndrome (CAMS) Type II
  • Cerebrotendinous Xanthomatosis
  • Cerebrotendinous Xanthomatosis
  • Cervical Schwannoma Presenting As Intracranial Posterior Fossa Subarachnoid Hemorrhage (SAH)
  • Cervical Spine Chordoma
  • Cervical spine dermal sinus tract (DST)
  • Cervical Tumoral Calcinosis
  • CHANTER (Cerebellar, Hippocampal, and Basal Nuclei Transient Edema with Restricted Diffusion) Syndrome
  • Charcot-Marie-Tooth (CMT)
  • CHARGE Syndrome
  • Chasing the Dragon (Heroin Leukoencephalopathy)
  • Chondroid Chordoma
  • Chondrosarcoma of the Cricoid Cartilage
  • Chordoid Glioma
  • Chordoid Meningioma
  • Chordoid Meningioma of the Third Ventricle
  • Chordoma
  • Chorea-acanthocytosis
  • Choroid Plexus Infarction
  • Choroid Plexus Infarction
  • Choroid Plexus Papilloma of the 4th Ventricle
  • Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
  • Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
  • Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive to Steroids (CLIPPERS)
  • Chronic Recurrent Multifocal Osteomyelitis (CRMO)
  • Cisternal Racemose Neurocysticercosis
  • Clear cell meningioma
  • Clival Aspergilloma
  • CNS Aspergillosis
  • CNS Cryptococcosis
  • CNS Nocardiosis
  • CNS Pheohyphomycoses (Fungal Infection)
  • CNS Posttransplant Lymphoproliferative Disorder (CNS-PTLD)
  • CNS Tuberculoma
  • CNS Whipple Disease
  • Cobb Syndrome (Spinal Arteriovenous Metameric Syndrome)
  • Coccidiodomycosis Spondylitis
  • Cochlear Incomplete Partition Type II and Large Vestibular Aqueduct
  • Cochlear (Intralabyrinthine) Schwannoma
  • Cochlear Otosclerosis
  • Cochlear (Retrofenestral) Otosclerosis
  • Cockayne Syndrome
  • Coloboma
  • Complete Carotid Artery Agenesis
  • Complete Labyrinthine Aplasia
  • Complete Labyrinthine Aplasia (CLA)
  • Congenital Afibrinogenemia
  • Congenital Cytomegalovirus Infection
  • Congenital Cytomegalovirus Infection
  • Congenital Epulis
  • Congenital Infiltrating Lipomatosis
  • Congenital Lipomatous Overgrowth, Vascular Malformations, Epidermal Nevi, and Skeletal Anomalies (CLOVES) Syndrome
  • Congenital Neuropathic Strabismus Due to Bilateral Third Cranial Nerve Hypoplasia/Aplasia
  • Congenital Piriform Aperture Stenosis
  • Congenital Unilateral Perisylvian Syndrome
  • Conjoined Nerve Roots
  • Copper Deficiency Myelopathy
  • (Corneal) Staphyloma, Anterior
  • Corpus Callosum Cavernous Malformation Bleeding into the Cavum Septum Pellucidum and Causing Noncommunicating Hydrocephalus
  • Cranial Fasciitis of Childhood
  • Craniofacial Parameningeal Rhabdomyosarcoma
  • Craniopharyngioma
  • Creutzfeldt-Jakob Disease
  • Creutzfeldt-Jakob Disease
  • Critical Illness–Associated Microbleeds
  • Crouzon Syndrome
  • Cryptococcosis
  • Currarino Syndrome (Incomplete Variant)
  • Cylindroma — Brooke-Spiegler Syndrome
  • Cyst of Velum Interpositum
  • Cystic Schwannoma of the Cauda Equina
  • Cysticercosis
  • Cytomegalovirus-Associated Ventriculitis and Chorioretinitis

D

  • Delayed Posthypoxic Leukoencephalopathy
  • Delayed Posthypoxic Leukoencephalopathy
  • Dengue Encephalitis
  • Dental Implant Migration
  • Dentatorubral-Pallidoluysian Atrophy (DRPLA)
  • Desmoplastic Infantile Ganglioglioma
  • Developmental Venous Anomaly
  • Developmental Venous Anomaly Associated with Unilateral Dystrophic Calcification of the Basal Ganglia and Thalamus
  • Diabetic Striatopathy
  • Pyruvate Dehydrogenase Complex (PDHc) Deficiency
  • Dialysis-Related Spondyloarthropathy
  • Diastematomyelia (Type 1)
  • Diastematomyelia with Intramedullary Dermoid
  • Diffuse Axonal Injury
  • Diffuse Axonal Injury
  • Diffuse Cerebral Anoxia
  • Diffuse Idiopathic Skeletal Hyperostosis (DISH) with Trans-Discal Fracture at L2-L3
  • Diffuse Infiltrating Retinoblastoma
  • Diffuse Intrinsic Pontine Glioma
  • Diffuse Leptomeningeal Glioneuronal Tumor
  • Diffuse Leptomeningeal Melanocytosis
  • Diffuse Pediatric-Type High-Grade Glioma H3-Wild-Type and IDH-Wild-Type, Optico-Chiasmatic Region
  • Dilated Perivascular Space of the Anterior Superior Temporal Lobe
  • Direct Carotid Cavernous Fistula
  • Direct Vertebral-Epidural Arteriovenous Fistula
  • Dissecting Aneurysm of the Main Arterial Feeder of a Vermian AVM
  • Disseminated Coccidiodomycosis
  • Disseminated Cysticercosis
  • Disseminated Hemangioblastomatosis
  • Disseminated Systemic Hydatidosis
  • Diving (Plunging) Ranula
  • Dorsal Thoracic Arachnoid Web
  • Down Syndrome with Atlantoaxial Instability and Persistent Ossiculum Terminale
  • Drug-Induced Intracranial Hypertension
  • Drug-Induced Chronic Hyperfluorosis
  • Duplicated Pituitary Gland
  • Duplication of the Pituitary Gland (DPG)-Plus Syndrome
  • Dural Arteriovenous Fistula (DAVF)
  • Dural Arteriovenous Fistula (DAVF), with Perimedullary Drainage
  • Dural Venous Sinus Laceration Complicating Extradural Hematoma
  • Dyke-Davidoff-Masson Syndrome with Crossed Cerebellar Atrophy
  • Dysembryoplastic Neuroepithelial Tumor (DNET)
  • Dysembryoplastic Neuroepithelial Tumor (DNET)
  • Dysmorphic Ear Ossicles in Fanconi Anemia
  • Dystrophic Calcification of Secondary Hyperparathyroidism

E

  • Eagle Syndrome
  • Ecchordosis Physaliphora
  • Ectopic Choroid Plexus in Chiari II Malformation
  • Ectopic Neurohypophysis
  • Ectopic Neurohypophysis, Absent Stalk, Hypoplastic Adenohypophysis
  • Ectopic Thymus Mimicking Lymph Node Metastasis
  • Ectopic Thyroid Gland (ETG)
  • EIGHTH NERVE NEUROPATHY SECONDARY TO SYSTEMIC LUPUS ERYTHEMATOSUS (SLE)
  • Embryonal Tumor with Multilayered Rosettes (ETMR)
  • Emphysematous Supraglottitis
  • Endolymphatic Sac Tumor (ELST)
  • Endophthalmitis
  • Epidermoid Cyst
  • Epidermoid, Intraventricular
  • Epidural Arteriovenous Fistula with Perimedullary Drainage
  • Epidural Lipomatosis with Post-operative Cord Infarct
  • Epidural Rosai-Dorfman Disease (RDD)
  • Epidural Spinal Hemangioma
  • Epstein-Barr Encephalitis
  • Erdheim-Chester Disease (ECD) with Involvement of the Central Nervous System
  • Erosive Arachnoiditis
  • Esthesioneuroblastoma
  • Ewing’s Sarcoma
  • External Auditory Canal Cholesteatoma
  • Extra-axial medulloblastoma, SHH-activated subtype
  • Extradural Spinal Arachnoid Cyst
  • Extradural Spinal Hemangioblastoma
  • Extramedullary hematopoiesis
  • Extramedullary Plasmacytoma
  • Extraosseous Primary Chordoma of the Nasopharynx
  • Extrapontine Diffuse Midline Glioma
  • Extraventricular Neurocytoma

F

  • Fabry's Disease
  • Facial Calcinosis in Lupus Erythematosus
  • Facial Nerve Schwannoma
  • Facial Nerve Schwannoma
  • Facial Ossifying Fibroma
  • Fahr's Disease
  • Fat Embolism
  • Febrile Illness–Related Status Epilepticus (FIRES)
  • Fetal Zika Infection
  • Fibrodysplasia Ossificans Progressiva
  • Fibrous Dysplasia of the Middle Turbinate
  • Focal Adhesive Arachnoiditis
  • Focal Cortical Dysplasia Type II
  • Fogging Effect
  • 4H Leukodystrophy
  • Fragile X–Associated Tremor/Ataxia Syndrome (FXTAS)
  • Frontal Lobe Intraparenchymal Schwannoma
  • Frontonasal Meningoencephalocystocele
  • Fukuyama Congenital Muscular Dystrophy
  • Fulminant Multiple Sclerosis
  • Fungal Abscess
  • FXTAS ( Fragile X Tremor Ataxia Syndrome)

G

  • Ganglioglioma
  • Ganglioglioma
  • Ganglioglioma with Malignant Transformation
  • Gardner Syndrome
  • Geniculate Ganglion Schwannoma
  • Giant Arachnoid Granulation
  • Giant Cavernous Angioma
  • Giant Cavernous Malformation
  • Giant Cavernous Sinus Hemangioma
  • Giant cell arteritis
  • Giant Cell Granuloma
  • Giant Cervical Lipoma
  • (Giant) Hemangiopericytoma
  • Giant Intracerebral Mature Tuberculoma
  • Giant Invasive Schwannoma
  • Giant Lateral Pterygoid Plate Osteochondroma
  • Giant Oral Cavity Teratoma
  • Giant Pterygopalatine Schwannoma
  • Giant Serpentine Aneurysm
  • Giant Temporal Intradiploic Arachnoid Cyst
  • Giant Thrombosed Posterior Cerebral Artery Aneurysm
  • Giant Tonsillolith Migration, Secondary Perforation, and an Associated Mediastinitis
  • Giant Virchow-Robin Space
  • Giant Virchow-Robin Spaces
  • Glioblastoma in Congenital Mismatch Repair Deficiency (CMMRD) Syndrome
  • Glioblastoma involving the optic nerve
  • Glioblastoma Multiforme of the Pineal Region
  • Gliomatosis Cerebri
  • Gliosarcoma
  • Global Anoxic/Hypotensive Cerebral Injury
  • Glomus Vagale
  • Glutaric Acidemia (Type 1)
  • Glutaric Aciduria Type 1 with Subependymal Nodules
  • GM1 Gangliosidosis (Adult-Onset Type)
  • Gobbi Syndrome
  • Gorham Disease (Vanishing Bone Disease)
  • Gorlin Syndrome
  • Granular Cell Tumor
  • Granulocytic Sarcoma (Chloroma/Extramedullary Myeloblastoma)
  • Granulocytic Sarcoma of the Spine
  • Granulomatous Amebic Encephalitis
  • Grisel Syndrome
  • Growing Skull Fracture
  • Guillain-Barré Syndrome
  • Gusher Ear in a Patient with Dysplastic Otic Capsule

H

  • Hadju-Cheney Syndrome
  • Hand-Schüller-Christian Disease
  • Heat Stroke
  • Hemangioblastoma
  • Hemangioblastoma
  • Hemangioblastomas in Von Hippel'Lindau Disease
  • Hemichorea-Hemiballismus Syndrome
  • Hemichorea-Hemiballismus Syndrome in Nonketotic Hyperglycemia
  • Hemimegalencephaly
  • Hemiplegic Migraine Headache
  • Hemolytic Uremic Syndrome
  • Hemolytic Uremic Syndrome–Associated Encephalopathy
  • Hemorrhagic Herpes Encephalitis
  • Hemorrhagic Vestibular Schwannoma
  • Hereditary Spastic Paraplegia
  • Herpes Encephalitis
  • Herpetic Trans-synaptic Lesion Affecting the Trigeminal Spinal Nucleus and Tract
  • HIGH ALTITUDE CEREBRAL EDEMA
  • High CBV due to Developmental Venous Anomaly (DVA)
  • Hirayama Disease
  • Hirayama Disease
  • HIV Encephalopathy Due to Congenital HIV Infection
  • HIV-related Lymphoepithelial Cysts
  • Horizontal Gaze Palsy with Progressive Scoliosis (HGPPS)
  • HSV-1 Encephalitis and Acute Cerebral Infarcts
  • Hunter Syndrome
  • Huntington Disease
  • Huntington Disease
  • Hurler's Syndrome
  • Hydatid Cyst
  • Hydrogen Peroxide Toxicity
  • Hyperammonemic Encephalopathy
  • Hyperglycemia-induced Hemiballism-hemichorea
  • Hyperparathyroidism-Jaw Tumor (HPT-JT) Syndrome
  • Hypertensive Brainstem Encephalopathy
  • Hypertrophic Olivary Degeneration
  • Hypertrophic Olivary Degeneration
  • Hypertrophic Olivary Degeneration (HOD)
  • Hypertrophic Olivary Degeneration (HOD)
  • Hypertrophy of Posterior Longitudinal Ligament
  • Hypoglossal Schwannoma
  • Hypoglossal Schwannoma
  • Hypoglycemic Encephalopathy
  • Hypoglycemic Encephalopathy
  • Hypoplasia of the Internal Carotid Artery with Intercavernous Anastomosis and Congenital Horner Syndrome
  • Hypothalamic Hamartoma
  • Hypothalamic Hamartoma
  • Hypoxic Ischemic Encephalopathy (HIE) and Cortical Laminar Necrosis

I

  • IAC Atresia with Aberrant Temporal Facial Nerve Canal
  • Idiopathic (Nonlesional) Bilateral Hypertrophic Olivary Degeneration
  • (Idiopathic) Foramen of Monro Stenosis/Atresia
  • Idiopathic Herniation of Gyrus Rectus
  • Idiopathic Intracranial Hypertension
  • Idiopathic Lumbosacral Epidural Lipomatosis
  • Idiopathic Neonatal Subpial Hemorrhage
  • (Idiopathic) Pneumoparotid
  • Idiopathic Spinal Cord Herniation
  • Idiopathic Thoracic Spinal Cord Herniation into a Vertebral Body
  • Idiopathic (viral?) Left CN VII Palsy
  • IgG4-Related Hypophysitis
  • Immune Effector Cell–Associated Neurotoxicity Syndrome (ICANS)
  • Incomplete Hanging with Regional Hyperperfusion
  • Incontinentia Pigmenti (IP)
  • Incudomalleolar Dislocation
  • Indirect Dural Arteriovenous Fistula of Left Cavernous Sinus
  • Infantile Krabbe Disease (Globoid Cell Leukodystrophy)
  • Infantile Krabbe Disease (KD)
  • Infantile Neuroaxonal Dystrophy (INAD)
  • Infected Remnant of 2nd Branchial Cleft Cysts
  • Infectious Aortic Aneurysm with Vertebral Involvement
  • Infectious Spondylodiscitis
  • Inflammatory Myofibroblastic Tumor
  • Inflammatory Pseudotumor (IPT) of the Brain
  • Internal Carotid Artery Agenesis
  • Intracept Procedure – Radiofrequency Ablation of Basivertebral Nerve
  • Intracranial Adhesive Arachnoiditis
  • Intracranial Arterial Dissection
  • Intracranial Cystic Cavernous Malformations
  • Intracranial Fat Embolism in a Patient with Vertebral Body Infarctions Due to Sickle Cell Anemia
  • Intracranial Gossypiboma/Textiloma
  • Intracranial Mesenchymal Chondrosarcoma
  • Intracranial Metal Emboli
  • Intracranial Metastasis in Fibrolamellar Hepatocellular Carcinoma
  • Intracranial Neurenteric Cyst
  • Intracranial Pre- and Paravertebral Rosai-Dorfman Disease (RDD)
  • Intracranial Ruptured Mature Teratoma
  • Intracranial Temporomandibular Joint Synovial/Ganglion Cyst
  • Intradural Extramedullary Tuberculoma of the Spinal Cord
  • Intradural Spinal Mature Teratoma
  • Intralabyrinthine Hemorrhage
  • Intramedullary Cavernoma
  • Intramedullary Mature Teratoma
  • Intramedullary Neurosarcoidosis
  • Intramedullary Spinal Cord Abscess
  • Intramedullary Spinal Cord Abscess Secondary to Infected Congenital Dermal Sinus
  • Intramedullary Spinal Cord Metastasis (ISCM) from Renal Cell Carcinoma
  • Intraorbital Epidermoid Cyst
  • Intraorbital Hydatid Cyst
  • (Intraosseous) Anterior Skull Base Meningioma
  • Intraosseous Hemangioma of Skull
  • Intraosseous Lipoma
  • Intraosseous Schwannoma
  • Intraspinal Epidermoid Cyst
  • Intravascular Large B-Cell Lymphoma (IVL)
  • Intraventricular Meningioma
  • Intraventricular Migration of Silicone Oil
  • Intraventricular Neurocysticercosis
  • Intraventricular Pilocytic Astrocytoma with Subependymal Metastases
  • Intraventricular Primary Central Nervous System Lymphoma
  • Intraventricular Schwannoma
  • Intraventricular Supratentorial Hemangioblastoma
  • Intravertebral Disc Cyst
  • Invasive Fungal Sinusitis with Optic Nerve Ischemia
  • Invasive Pituitary Adenoma
  • Iodide-Induced Sialoadenitis
  • Ipilimumab-Induced Hypophysitis
  • Irreversible Cortical Blindness in Nonketotic Hyperglycemia
  • Isolated Cortical Vein Thrombosis
  • Isolated Cortical Vein Thrombosis Mimicking Brain Neoplasm
  • Isolated Hypothalamic Metastasis from Lung Cancer
  • Isolated Nasopharyngeal Amyloidoma
  • Isoniazid Toxicity

J

  • Joubert Syndrome-Related Disorders (JSRD)
  • Jugular Schwannoma
  • Juvenile Nasopharyngeal Angiofibroma (JA)
  • Juvenile Recurrent Parotitis

K

  • Kallmann Syndrome
  • Kearns-Sayre Syndrome (KSS)
  • Kearns-Sayre Syndrome (KSS)
  • Kikuchi Disease (Histiocytic Necrotizing Lymphadenitis)
  • Kimura Disease
  • Kimura’s Disease
  • Klippel-Feil Syndrome
  • Kratom Neurotoxicity

L

  • L-2 Hydroxyglutaric Aciduria
  • L-carnitine deficiency with associated thalmic hemorrhage
  • Labyrinthitis Ossificans
  • Labyrinthitis Ossificans (Fibrous Stage)
  • Labyrinthitis Ossificans (Ossifying Stage)
  • Langerhans Cell Histiocytosis
  • Langerhans Cell Histiocytosis
  • Langerhans cell histiocytosis (Eosinophilic granuloma)
  • Langerhans Cell Histiocytosis (LCH)
  • Langerhans Cell Histiocytosis (LCH) of the Spine
  • Langerhans Cell Histiocytosis of the Hypothalamic Pituitary Axis
  • Laryngeal Tuberculosis
  • Late-Onset Pompe Disease
  • Lead Encephalopathy
  • Leigh Disease
  • Leigh's Syndrome
  • Lemierre Syndrome
  • Lemierre Syndrome
  • LENTICULOSTRIATE ARTERY DISSECTING ANEURYSM
  • Lenticulostriate Vasculopathy (LV)
  • Leptomeningeal Familial Amyloidosis
  • Leptomeningeal Lipomatous Hamartomas with Associated Dysplastic Cortex
  • Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Lactate Elevation (LBSL)
  • Levamisole Leukoencephalopathy
  • Levator Claviculae Muscle
  • Levator Scapulae Cysticerosis
  • Lhermitte-Duclos Disease
  • Limited Dorsal Myeloschisis, Nonsaccular Type
  • Linear Scleroderma
  • Lingual Artery Pseudoaneurysm and Neopharynx Dehiscence Status Post Total Laryngectomy
  • Lingual Thyroid
  • Lipedematous scalp
  • Lipoid Proteinosis: Bilateral Amygdalae Calcifications
  • Lipomatous Meningioma
  • Lipomatous meningioma
  • Lipomyelocele with ossified dysraphic hamartoma
  • Listeria Rhombencephalitis
  • Listerial Rhombencephalitis
  • Lobular Capillary Hemangioma
  • Lowe (Oculocerebrorenal) Syndrome
  • Lymphangiomatous Polyp
  • Lymphocytic Hypophysitis
  • Lymphomatous Meningitis from Diffuse Large B-Cell Lymphoma (DLBCL)

M

  • Malignant Fibrous Histiocytoma (pleomorphic undifferentiated sarcoma) of the Larynx
  • Malignant Melanotic Nerve Sheath Tumor (MMNST)
  • Malignant Peripheral Nerve Sheath Tumor (MPNST)
  • Maple Syrup Urine Disease
  • Maple Syrup Urine Disease
  • Marchiafava-Bignami Disease
  • Marchiafava-Bignami Disease
  • Marchiafava-Bignami Disease
  • Maxillary Sinus Squamous Cell Cancer with Involvement of 2nd Div. of left Trigeminal Nerve
  • Medulloblastoma
  • Medulloblastoma with Extensive Nodularity
  • Medulloepithelioma of the Ciliar Body
  • Megalencephalic Leukoencephalopathy with Subcortical Cysts
  • Megalencephalic Leukoencephalopathy with Subcortical Cysts (MLC) 1 in an Adult
  • Megalencephalic Leukoencephalopathy with Subcortical Cysts (MLC)
  • Melanotic Neurectodermal Tumor of Infancy
  • Meningeal Inflammatory Myofibroblastic Tumor
  • Meningeal Melanocytoma
  • Meningeal Melanocytosis
  • Meningioangiomatosis
  • Meningioangiomatosis
  • Meningioangiomatosis with Associated Meningioma
  • Meningitis, Ventriculitis, and Liquefaction of Periventricular White Matter (Citrobacter koseri)
  • Meningovascular Syphilis
  • Mesencephalic Exophytic Cavernous Malformation
  • Mesenchymal Chondrosarcoma of the Neck
  • Mesial Temporal Sclerosis
  • Metachromatic Leukodystrophy
  • Metachromatic Leukodystrophy
  • Metastasic Ganglioneuroblastoma in the Orbit
  • Metastatic Neuroblastoma
  • Methanol Intoxication
  • Methanol Intoxication
  • Methanol Toxicity
  • Methotrexate-Induced Neurotoxicity
  • Metronidazole-Induced Encephalopathy
  • Metronidazole-Induced Toxic Encephalopathy
  • Middle Cerebellar Peduncle and Corticospinal tract Wallerian Degeneration Secondary to Pontine Infarction
  • Middle Interhemispheric Variant of Holoprosencephaly
  • Midline Craniofacial-Cerebral Dysraphism
  • Midline Spinal Cord Hamartoma
  • Miliary Brain Tuberculosis
  • Mitochondrial Disease with Heterozygous NUBPL Mutation
  • Mitochondrial Encephalopathy Lactic Acidosis and Stroke-Like Episodes (MELAS)
  • Mitochondrial Encephalopathy Lactic Acidosis Stroke-Like Episodes (MELAS)
  • Mixed Hearing Loss due to Aberrant Position of the Right Facial Nerve
  • Morning glory disc anomaly (MGDA) with associated abnormalities
  • Moyamoya Disease
  • Moyamoya Disease
  • Mucopolysaccharidosis Type 1 (Hurler Syndrome)
  • Multifocal Glioblastoma
  • Multinodular and Vacuolating Neuronal Tumor of the Cerebrum (MVNT)
  • Multinodular and Vacuolating Posterior Fossa Lesions of Unknown Significance (MV-PLUS)
  • Multiple cavernomas of the corpus callosum
  • Multiple Intracranial Myxomatous Aneurysms
  • Multiple Meningiomas in NF-2
  • Multiple Nonsyndromic Schwannomas
  • Multiple System Atrophy
  • Multiple System Atrophy — Cerebellar Type
  • Multiple System Atrophy-Parkinson Type (MSA-P)
  • Murray Valley Encephalitis
  • Mycotic/Infectious Aneurysm
  • Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease (MOGAD)
  • Myeloid Sarcoma of the Cavernous Sinus – JAK2-Positive Myeloproliferative Disorder with Acute Myeloid Leukemia Transformation
  • Myofibroma
  • Myotonic Dystrophy (Steinert Disease)
  • Myotonic Dystrophy Type 1
  • Myxopapillary Sacrococcygeal Ependymoma

N

  • Nasal Dermal Sinus (with Incidental Associated Nasal Fracture)
  • Nasal Mucormycosis with Invasion of Skull Base
  • Nasal Septal Abscess
  • Nasopalatine Duct Cyst
  • Neonatal Candida Albicans Brain Abscesses
  • Neonatal Endophthalmitis
  • Neonatal Parechovirus (HPeV) Encephalitis
  • Neurenteric Cyst
  • Neurenteric Cyst
  • Neuroacanthocytosis
  • Neuroborreliosis
  • Neurobrucellosis
  • Neurocutaneous Melanosis
  • Neurocysticercosis (NCC)
  • Neuroendocrine Tumor of the Middle Ear Cavity
  • Neuroferritinopathy
  • Neurofibromatosis 2 with MISME Syndrome
  • Neurofibromatosis Type 2
  • Neuroglial Heterotopia (Nasal Glioma)
  • Neuromyelitis Optic (Devic disease)
  • Neuromyelitis Optica (NMO)
  • Neurosarcoidosis
  • Neurosarcoidosis
  • Neurosarcoidosis
  • Neurosarcoidosis
  • Neurosarcoidosis
  • Neurosyphilis
  • Neurosyphilis
  • Neurosyphilis
  • Neurosyphilis - Otosyphilis
  • NF-1, Extensive Plexiform Neurofibromas
  • NF-2, Meningioma, Multiple Schwannomas
  • Nitrous Oxide Abuse–Related Myelopathy
  • Nivolumab Autoimmune Limbic Encephalitis (ALE)
  • Non-Hodgkin Lymphoma of Nasal Cavity and Paranasal Sinuses – Natural Killer Cell Type
  • Nonalcoholic Wernicke Encephalopathy
  • Nonketotic Hyperglycemic Hemichorea (NHH)
  • Nonketotic Hyperglycinemia (NKH)
  • Nonsecretory Pituitary Macroadenoma
  • Nonsyndromal Multisuture Synostosis
  • Norrie Disease

O

  • Ocular Cysticercosis
  • Oculo-Auriculo-Vertebral Spectrum/Goldenhar Syndrome
  • Olfactory Neuroblastoma
  • Olfactory Neuroblastoma (ONB)
  • Opercular Syndrome due to Bilateral Perisylvian Polymicrogyria
  • Ophthalmoplegic Migraine
  • Optic Nerve Hypoplasia (ONH)
  • Oral Hemangioma
  • Oral-Facial-Digital Syndrome Type VI
  • Orbital and Neck Emphysema (Secondary to Extensive Nose Blowing)
  • Orbital Cavernous Hemangioma
  • Orbital Cellulitis and Subperiosteal Abscess
  • Orbital Cylindroma
  • Orbital Foreign Bodies
  • Orbital Hydatid Cyst
  • Orbital Lipolysis
  • Orbital Lymphoma with Perineural Spread
  • Orbital Pseudotumor
  • Orbital Varix
  • Orbital Venous-Lymphatic Malformation (OVLM) (Lymphangiomas)
  • Orbital Wooden Foreign Body
  • Orbital Xanthoma (Adult Onset Xanthogranuloma)
  • Osmotic Demyelination Syndrome
  • Osmotic Demyelination Syndrome
  • Osmotic Demyelination Syndrome (ODS)
  • Ossification of Posterior Longitudinal Ligament
  • Ossifying Fibroma
  • Osteopathia Striata with Cranial Sclerosis
  • Osteosarcoma of the Maxillary Sinus
  • Otogenic Septic Jugular Vein Thrombophlebitis (Lemierre’s Syndrome) with s. pyogenes bacteremia

P

  • Pantothenate Kinase-Associated Neurodegeneration (PKAN)
  • Papillary Glioneuronal Tumor
  • Papillary Tumor of the Pineal Region
  • Papillary Tumor of the Pineal Region (PTPR)
  • Paradoxical Cerebral Herniation
  • Parahippocampal Gray Matter Heterotopias, Dysplastic Left Cerebellum
  • Paraneoplastic Limbic Encephalitis
  • Parry Romberg Syndrome (PRS)
  • Parry-Romberg Syndrome
  • Parsonage-Turner Syndrome
  • Parsonage-Turner Syndrome
  • Pediatric Intervertebral Disc Calcification
  • Pelizaeus-Merzbacher Disease (PMD)
  • Perimesencephalic Subarachnoid Hemorrhage (PMSAH)
  • Perineural cysts associated with autosomal dominant polycystic kidney disease (ADPKD)
  • Perineural spread of squamous cell carcinoma to the greater auricular nerve
  • Perineural Spread on FDG-PET/CT
  • Perioperative Ischemic Optic Neuropathy
  • Peripheral Primitive Neuroectodermal Tumor
  • Perisylvian lipoma associated with a left lentiform nucleus infarct
  • Persistent Hyperplastic Primary Vitreous (PHPV)
  • Persistent Hypoglossal Artery
  • Persistent hypoglossal artery with synchronous left internal carotid and basilar artery occlusion
  • Persistent Primitive Hypoglossal Artery with Ipsilateral ICA Occlusion, Left
  • Persistent Stapedial Artery (PSA)
  • Persistent Trigeminal Artery
  • Petrous Apex Cephalocele
  • Petrous Apex Chondrosarcoma in Ollier Disease (Enchondromatosis)
  • Petrous ICA Aneurysm
  • Petrous ICA Dissection
  • Petrous Internal Carotid Artery Aneurysm
  • Pigmented Villonodular Synovitis of the Temporomandibular Joint
  • Pilocytic Astrocytoma
  • Pilocytic Astrocytoma of the Spinal Cord
  • Pilomyxoid Astrocytoma
  • Pineal Parenchymal Tumor of Intermediate Differentiation, WHO grade 3
  • Pineoblastoma
  • Piriformis syndrome caused by a split piriformis muscle
  • Pituitary Abscess
  • Pituitary Apoplexy
  • Pituitary Apoplexy with Subarachnoid Hemorrhage and Todd Paralysis
  • Pituitary Carcinoma
  • Pituitary Macroadenoma
  • Pituitary Macroadenoma in the Setting of Multiple Endocrine Neoplasia (MEN) Type 1
  • Pituitary Siderosis
  • Pituitary Stalk Tuberculoma
  • Pituitary Stone
  • Pleomorphic Adenoma of the Parotid Gland
  • Pleomorphic Xanthoastrocytoma (PXA)
  • Pneumorrhacis
  • POEMS Syndrome
  • POLR3B Homozygous Mutation (Hypomyelinating Leukodystrophy-8)
  • Polyarteritis Nodosa
  • Polymicrogyria/Congenital CMV
  • Polymorphous Low-grade Neuroepithelial Tumor of the Young
  • Polymorphous Low-Grade Neuroepithelial Tumor of the Young (PLNTY)
  • Pontine and Extrapontine Osmotic Demyelination Syndrome
  • Pontine Tegmental Cap Dysplasia
  • Post Laminectomy Gossypiboma
  • Post-traumatic Superficial Temporal Artery Pseudoaneurysm
  • Posterior Epidural Cyst Associated with Baastrup Disease
  • Posterior Epidural Migration of Sequestrated Disc
  • Posterior Fossa Pilocytic Astrocytoma without Gangliocytic Differentiation
  • Posterior Quadrantic Dysplasia
  • Posterior Reversible Encephalopathy Syndrome
  • Posterior Reversible Encephalopathy Syndrome (PRES)
  • Posterior Spinal Artery Syndrome Following Thrombotic Occlusion of the Vertebral Artery
  • Postictal Signal Changes
  • Postpartum Hypernatremic Osmotic Demyelination
  • Posttraumatic CSF Oculorrhea Secondary to Cranio-Orbital Fistula
  • Posttraumatic Sialocele of the Submandibular Gland
  • Pott's Puffy Tumor
  • Prevertebral (Longus Coli) Calcific Tendinitis
  • Primary bilateral parotid Non-Hodgkin lymphoma (MALT Type)
  • Primary CNS Lymphoma (PCNSL) in an Immunocompetent Patient
  • Primary CNS T Cell Lymphoma (Lymphomatosis Cerebri Pattern)
  • Primary Extradural Meningioma
  • Primary Extradural Meningioma
  • Primary Extradural Meningioma
  • Primary Familial Brain Calcification
  • Primary Intraosseous Meningioma
  • Primary Lateral Sclerosis (PLS) with adaptive compensatory functional changes
  • Primary Leptomeningeal Lymphoma
  • Primary Melanoma of Cerebellopontine Angle
  • Primary Nasopharyngeal Non-Hodgkin Lymphoma
  • Primary Pachymeningeal (Dural) CNS Lymphoma
  • Primary Paranasal Sinus Diffuse Large B-cell Non-Hodgkin Lymphoma
  • Progressive Multifocal Leukoencephalopathy
  • Progressive Multifocal Leukoencephalopathy
  • Progressive Multifocal Leukoencephalopathy
  • Progressive Supranuclear Palsy
  • Psammomatoid Ossifying Fibroma
  • Psammomatous Meningioma
  • Pseudohypoparathyroidism
  • Pseudo-Subarachnoid Hemorrhage
  • Pseudotumor Hemicerebellitis
  • Pterygoid Hamulus Syndrome
  • Pyogenic Brain Abscess

R

  • Rabies Encephalomyelitis
  • Radiation Myelopathy (RM)
  • Radiation necrosis mimicking tumor progression
  • Radiation Necrosis with Delayed Cyst Formation
  • Radiation-induced osteosarcoma of the greater sphenoid wing
  • Radiation-Induced Tumefactive Cyst (RITC)
  • Radiation-induced vasculopathy with pontine hematoma
  • Radiculopial Artery Aneurysm Rupture
  • Ramsay Hunt Syndrome
  • Ramsay Hunt Syndrome
  • RANBP2 mutation-related Acute Necrotizing Encephalopathy Type 1 (ANE1)
  • Rathke Cleft Cyst
  • Rathke's Cleft Cyst
  • Rathke's Cleft Cyst (Congenital Mucinous Cyst) of the Pituitary Stalk
  • Recurrent Cholesteatoma
  • Remote Cerebellar Hemorrhage
  • Remote Cerebellar Hemorrhage
  • Remote supratentorial Hemorrhage
  • Renal Osteodystrophy with Brown Tumors
  • Respiratory Epithelial Adenomatoid Hamartoma (REAH)
  • Rete M1 Anomaly
  • Reversible Cerebral Vasoconstriction Syndrome
  • Reversible Cerebral Vasoconstriction Syndrome (RCVS)
  • Reversible Focal Splenial Lesion
  • Rhabdomyosarcoma of Orbit
  • Rheumatoid Meningitis
  • Rhino-Orbito-Cerebral Mucormycosis (ROCM)
  • Rhinocerebral Mucormycosis with Perineural Spread Pattern
  • Rhombencephalosynapsis
  • Rhombencephalosynapsis
  • Rocky Mountain Spotted Fever (RMSF)
  • Rosai-Dorfman Disease
  • Rosai-Dorfman Disease
  • Rosai-Dorfman Disease
  • Rosette-Forming Glioneuronal Tumor: Hypothalamic Origin
  • Ruptured Dermoid Cyst at the Cervicomedullary Junction with Intraventricular Dissemination
  • Ruptured Infectious Aneurysm
  • Ruptured Isolated PICA Dissecting Aneurysm
  • Ruptured Mycotic ICA Aneurysm with Invasive Sphenoid Sinusitis
  • Ruptured Pontine Arteriovenous Malformation
  • Ruptured Spinal Cord Dermoid

S

  • Sacral Agenesis
  • Sacral Giant Cell Tumor
  • Sacral Insufficiency Fracture
  • Sacrococcygeal Teratoma
  • Salla Disease
  • Sarcoid Meningoencephalitis
  • Sarcoidosis
  • Schimmelpenning-Feuerstein-Mims syndrome (SFMS)
  • Schizencephaly
  • Schwannoma mimicking MPE
  • Scleritis
  • Scrofula
  • Scrub Typhus Meningoencephalitis
  • Scwhannoma
  • Second Branchial Cleft Cyst
  • (Secondary) Hemochromatosis
  • Segmental Spinal Dysgenesis (SSD)
  • Semilobar Holoprosencephaly
  • Septo-Optic Dysplasia Syndrome
  • Serous Fat Atrophy
  • Sialoblastoma
  • Silent Sinus Syndrome
  • Sinonasal Eosinophilic Angiocentric Fibrosis
  • Sinonasal Organized Hematoma
  • Sinonasal Schwannoma
  • Sinonasal Squamous Cell Carcinoma Presenting as a Clival Mass
  • Sinonasal Undifferentiated Carcinoma (SNUC)
  • Sinus Pericranii
  • Skull Anuerysmal Bone Cyst
  • Skull Base Meningioma with Perineural Spread 
  • Skull Base Osteomyelitis (SBO)
  • Skull Parosteal Lipoma With Reactive Hyperostosis
  • SMART Syndrome
  • Sneddon Syndrome
  • Solitary Extrapleural Fibrous Tumor
  • Solitary Fibrous Tumor
  • Spastic Paraplegia-47 (AP4B1 related AP-4 deficiency)
  • Sphenoid Encephalocele
  • Spinal Arachnoid Cyst with Intramedullary Extension
  • Spinal Arteriovenous Fistula
  • Spinal Arteriovenous Malformation
  • Spinal Cord Arteriovenous Malformation (Type III)
  • Spinal Cord Cavernous Malformation
  • Spinal Cord Compression Secondary to Ossification of Ligamentum Flavum and Epidural Lipomatosis
  • Spinal Cord Decompression Sickness (SCDS)
  • Spinal Cord Glioblastoma Multiforme
  • Spinal Cord Infarct
  • Spinal Cord Infarct with Vertebral Body Infarct
  • Spinal Cord Infarction
  • Spinal Cord Subependymoma
  • Spinal Cystic Echinococcosis (Hydatid Disease)
  • Spinal Dermoid
  • Spinal Dermoid
  • Spinal Dural Arteriovenous Fistula (SDAVF)
  • Spinal Epidermoid Cyst Post–Myelomeningocele Repair
  • Spinal Epidural Angiolipoma
  • Spinal Epidural Angiolipoma
  • Spinal Epidural Hemangioma
  • Spinal Gout Causing Spinal Cord Compression
  • Spinal Hydatid Cyst
  • Spinal Intradural Capillary Hemangioma
  • Spinal Meningeal Melanocytoma
  • Spinal Neuroendocrine Tumor
  • Spinocerebellar Ataxia
  • Spontaneous Epidural Hematoma
  • Spontaneous Intracranial Hypotension
  • Spontaneous Spinal Epidural Hematoma (SSEH) in the Postpartum Period
  • Squamous Cell Carcinoma
  • St. Louis Encephalitis (SLEV)
  • Sturge Weber Syndrome
  • Sturge-Weber Syndrome
  • Stylocarotid Artery Syndrome (Eagle Syndrome, Vascular Variant)
  • Subacute Combined Degeneration
  • Subacute Labyrinthitis
  • Subacute Right Thalamic Infarction
  • Subacute Sclerosing Panencephalitis
  • Subarachnoid Hemorrhage (SAH) from Ruptured Persistent Hypoglossal Artery (PHA) Aneurysm
  • Subconjunctival Fat Prolapse
  • Subdural Hematoma from a Ruptured Pericallosal Artery Aneurysm
  • Subependymal Giant Cell Astrocytoma in Tuberous Sclerosis
  • Subependymoma
  • Sublingual Dermoid Cyst
  • SUBMENTAL DERMOID CYST OF FLOOR OF MOUTH (IN A PATIENT WITH LEFT BUCCAL MUCOSA SQUAMOUS CELL CARCINOMA)
  • Subperiosteal Osteoid Osteoma
  • Superficial Siderosis Secondary to a Paraganglioma
  • Superficial Siderosis (SS)
  • Suprasellar Cavernoma
  • Supratentorial CNS Embryonal Tumor (formerly PNET)
  • Surfer's ear - Exostosis of External Auditory Canal
  • Susac Syndrome
  • Susac's Syndrome
  • SYNOVIAL SARCOMA
  • Systemic Lupus Erythematosus-associated Optic Neuritis and Acute Infarction

T

  • T2-FLAIR Mismatch in IDH-Mutated Glioma (Anaplastic Astrocytoma)
  • T2-Weighted Hypointensity in Partial Status Epilepticus
  • Tabes Dorsalis
  • Tabes Dorsalis (Syphilitic Myelitis)
  • Tectal Glioma
  • Temporal Bone Fracture
  • Tenosynovial Giant Cell Tumor (TGCT), Localized Type
  • Tension Pneumocephalus with “Mount Fuji” Sign
  • Terson Syndrome
  • Thrombosed Giant Vertebral Artery Aneurysm
  • Thrombosis of the Superior Sagittal, Left Transverse and Left Sigmoid Sinuses
  • Thrombosis, Straight Sinus and Deep Cerebral Veins
  • Thyroglossal Duct Cyst Papillary Carcinoma
  • Thyroid Cartilage Chondrosarcoma
  • TMJ Synovial Chondromatosis
  • Tolosa-Hunt Syndrome
  • Tolosa-Hunt Syndrome Caused by Tuberculosis
  • Toxoplasmosis
  • Toxoplasmosis
  • Transient Global Amnesia
  • Transient Global Amnesia
  • Transient Global Amnesia
  • Transient Global Amnesia
  • Transient Splenial Lesion Due to Hypoglycemia
  • Transmantle Cortical Dysplasia (with Closed Lip Schizencephaly)
  • Transmodiolar Intralabyrinthine Schwannoma
  • Transthyretin-Associated Amyloidomas
  • Transverse Temporal Bone Fracture with Pneumolabyrinth
  • Trapped Ventricle Secondary to CNS Tuberculosis
  • Traumatic Carotid Cavernous Fistula (Barrow Type A)
  • Traumatic Middle Meningeal Artery Pseudoaneurysm
  • Traumatic Pericallosal Artery Dissection
  • Traumatic Vertebral Artery Injury (Dissecting Pseudoaneurysm)
  • Trigeminal Hypoplasia
  • Trigeminal Schwannoma (V2 and V3)
  • Trochlear Schwannoma with Superior Oblique Atrophy
  • Trochleitis with Acquired Brown Syndrome
  • Trousseau Syndrome
  • True Congenital Hemifacial Hyperplasia with Unique Intraorbital Involvement
  • Tuberculosis Hypophysitis
  • Tuberculous Brain Abscess
  • Tuberculous Meningitis
  • Tuberculous Meningitis with Acute Infarct with Longitudinally Extensive Transverse Myelitis
  • Tuberculous Spondylitis
  • Tuberous Sclerosis
  • Tuberous Sclerosis
  • Tubulinopathy
  • Tumefactive Demyelinating Lesion
  • Tumefactive Demyelinating Lesions
  • Tumoral Calcinosis (TC) in Scleroderma
  • Type 2 Branchial Cyst
  • (Type 4) Cystic Meningioma

U

  • Unilateral Cerebellar Hypoplasia
  • Unilateral Kallmann Syndrome with Associated GM Heterotopias
  • Unilateral Membranous Choanal Atresia
  • Unilateral Submandibular Gland Aplasia
  • Uremic Encephalopathy with Lentiform Fork Sign
  • Uremic Leontiasis Ossea

V

  • Vagal Schwannoma
  • Vanishing white matter (VWM) disease
  • Varicella zoster virus vasculopathy (with proved positive VZV DNA in the CSF)
  • Varicella-Zoster Vasculitis and Stroke
  • Venolymphatic Facial Malformation
  • Ventriculus Terminalis
  • Vertebral Artery Transection Secondary to Penetrating Trauma
  • Vogt-Koyanagi-Harada syndrome (VKH)
  • Von Hippel-Lindau
  • Von Hippel-Lindau Disease

W

  • Wallerian Degeneration of the Pontocerebellar Fibers
  • Wegener Granulomatosis
  • Wernicke Encephalopathy after Bariatric Surgery
  • Wernicke's Encephalopathy
  • West Nile Virus Myelitis (Serum IgM +)
  • WHO Grade 1 Cystic Meningioma (Type I/II)
  • Wilson Disease
  • Wilson's Disease
  • Wolfram Syndrome
  • Wolfram Syndrome (DIDMOAD)

X

  • X-Linked Adrenoleukodystrophy (ALD)
  • X-Linked Adrenoleukodystrophy (ALD)

“

  • “Pancake-like” Contrast Enhancement in Cervical Spondylotic Myelopathy
  • “White” epidermoid cyst

Current Issue

American Journal of Neuroradiology: 45 (12)
American Journal of Neuroradiology
Vol. 45, Issue 12
1 Dec 2024
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Print ISSN: 0195-6108 Online ISSN: 1936-959X

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