Articles

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More than 200 results
Article

Primary melanocytic tumors of the CNS

Primary melanocytic tumors of the central nervous system are a group of related neoplasms of variable aggressiveness which are thought to arise from leptomeningeal melanocytes which are of neural crest origin.  Under the 2016 WHO classification of CNS tumors, four entities are recognized 1:  me...
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External capsule

The external capsule is a series of white matter tracts in the brain situated between the putamen and claustrum. It is composed of claustrocortical fibers dorsally and the combined mass of the uncinate fasciculus and inferior frontal occipital fasciculus ventrally. Relationships The lentiform ...
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Sinonasal mucormycosis

Sinonasal mucormycosis refers to an uncommon form of invasive fungal sinus infection. Given its highly invasive nature, it can involve orbits and/or intracranial structures. Clinical presentation The presentation can vary, ranging from exophthalmos, rhinorrhea, and ophthalmoplegia with loss of...
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Stasis filling

Stasis filling describes persistent visualization of intravenous contrast within the proximal cerebral arteries but not within the cortical branches or venous outflow in suspected brain death patients, mimicking true cerebral blood flow (CBF). Pathology Etiology During brain death, raised int...
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Pulvinar (disambiguation)

Pulvinar may refer to: pulvinar thalamic nuclei (classically involved in variant Creutzfeldt-Jakob disease, see pulvinar sign) Haversian fat pad of the hip (which covers the central non-articular part of the acetabulum)
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Infant-type hemispheric glioma

Infant-type hemispheric gliomas, also known as infant high-grade gliomas, are high-grade brain tumors occurring in children. Terminology Infant-type hemispheric gliomas belong to the family of "pediatric high-grade diffuse gliomas" of the 2021 WHO Classification of Tumors of the Central Nervou...
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Spinal muscular atrophy

Spinal muscular atrophy is a type of congenital neuromuscular disease affecting anterior horn cells of the brainstem and spinal cord. Epidemiology This disorder affects 1 in 6000-10000 infants 1. Clinical presentation Spinal muscular atrophy typically affects infants and young children, pres...
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Trotter syndrome

Trotter syndrome relates to advanced nasopharyngeal carcinoma and is the constellation of: unilateral conductive hearing loss due to middle ear effusion trigeminal neuralgia due to perineural spread soft palate immobility
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Calcar avis

Calcar avis is an elevation of white matter projecting from the medial wall of the occipital horn of the lateral ventricle. It is variably conspicuous, depending on how deep the calcarine sulcus is. Gross anatomy The calcar avis is located on the medial wall of the occipital horn, near the ju...
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Watershed cerebral infarction

Watershed cerebral infarctions, also known as border zone infarcts, occur at the border between cerebral vascular territories where the tissue is furthest from arterial supply and thus most vulnerable to reductions in perfusion.  Epidemiology Watershed cerebral infarction accounts for 5-10% of...
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Anterior inferior cerebellar artery

The anterior inferior cerebellar artery (AICA) is one of three vessels that provides arterial blood supply to the cerebellum. It has a variable origin, course and supply, with up to 40% of specimens not having an identifiable standard AICA. The amount of tissue supplied by the AICA is variable (...
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Focal cortical dysplasia

Focal cortical dysplasias (FCD) represent a heterogeneous group of disorders of cortical formation, which may demonstrate both architectural and proliferative features. They are one of the most common causes of epilepsy and can be associated with hippocampal sclerosis and cortical glioneuronal n...
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Tuberous sclerosis

Tuberous sclerosis (TS), also known as tuberous sclerosis complex (TSC) or Bourneville disease, is a phakomatosis (neurocutaneous disorder) characterized by the development of multiple benign tumors of the embryonic ectoderm (e.g. skin, eyes, and central nervous system). Epidemiology Tuberous ...
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Ependymoma vs astrocytoma of the spinal cord

A number of factors are useful when differentiating between spinal cord ependymoma and spinal cord astrocytoma.  Ependymoma child or adult more central in location well-defined lesion bone remodeling is common low T1 signal well-defined enhancement syrinx is more common hemorrhage is mo...
Article

Neonatal herpes simplex encephalitis

Neonatal herpes simplex encephalitis is caused by vertical transmission of infection during passage from birth canal with diffuse cerebral involvement within the first month after birth; in contrast to adult herpes simplex encephalitis, it is commonly related to HSV-2.  Epidemiology The incide...
Article

Crista galli

The crista galli is a thick, midline, smooth triangular process arising from the superior surface of the ethmoid bone, projecting into the anterior cranial fossa. It separates the olfactory bulbs, which lie on either side of it in the olfactory fossae of the cribriform plate. It serves as an ant...
Article

Paraphysis elements

The so-called paraphysis elements are embryonic structures which appears like a thin strand between telencephalon and the anterior portions of diencephalon 1. It is believed to be the structure which results in colloid cysts of the third ventricle.
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Boston criteria 2.0 for cerebral amyloid angiopathy

The Boston criteria 2.0 were proposed in 2022 in order to better include leptomeningeal and white matter characteristics into the diagnoses of probable and possible cerebral amyloid angiopathy (CAA) 1. They consist of combined clinical, imaging and pathological parameters, and are based upon the...
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Metachromatic leukodystrophy

Metachromatic leukodystrophy (MLD) is the most common hereditary (autosomal recessive) leukodystrophy and is one of the lysosomal storage disorders. It has characteristic imaging features including peri-atrial and to a lesser extent frontal horns leukodystrophy as well as periventricular periven...
Article

Contrast-induced neurotoxicity

Contrast-induced neurotoxicity, also known as iodinated contrast-induced encephalopathy, is a rare complication of iodinated intravascular contrast resulting in a usually temporary neurological deficit. CT imaging findings can be dramatic, demonstrating contrast staining and edema, but spontaneo...

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