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57 Cards in this Set

  • Front
  • Back

What systemic disease is associated with giant cell astrocytoma

tuberous sclerosis Neurofibromatosis
What systemic disease is associated with astrocytomas, optic neuromas and enlargement of middle cranial fossa?
neurofibromatosis type 1
What is the earliest manifiestation of neurofibromatosis type 1?
cafe au lait spots.

name a skeletal manifestation of NF1

dysplasia of the scapula
Tegmentum is located
ventral to the cerebral aqueduct
under the microscope, what is difficult to differentiate from DNET?

oligodendroglioma.

What kind of glial cells are choroid plexus cells most similar to?

Ependymal cells
What is a thornwaldt cyst?
midline nasopharyngeal mucosal cyst.

Brainstem glioma demographic (mean age in years)

Paediatric
Pars compacta is a part of the

substantia nigra

Describe the WHO classification for astrocytomas?

localized astrocytoma WHO grade I, diffuse astrocytoma WHO grade II, anaplastic astrocytoma, GBM
benign intraventricular neuroepithelial tumour with a cauliflower-like appearance (and DDx)
Choroid plexus papiloma
Where do astrocytomas typically occur in children?

posterior fossa, hypothalamus, optic chiasm

What is the thin epithelium-like lining of the ventricular system and spinal cord called?

Ependyma
what does PNET stand for?
primative neuroectodermal tumour
Most aggressive malignant primary brain tumor in humans

Glioblastoma multiforme

MR findings in wernicke's encephalopathy
bilateral medial thalamic T2 hyperintensity
Pars compacta is a part of the
substantia nigra
What are the 3 types of glial cells
astrocytes, oligodendrocytes, ependymal cells
most common posterior fossa tumor in children
medulloblastoma (35%)
from where does medulloblastoma usually arise?
superior medullary velum
what is the superior medullary velum?
thin lamina of white matter extending between the superior cerebral peduncles and forming the roof of the 4th ventricle.
Glioblastoma multiforme is often compared to the shape of a
butterfly
DDx for midline septumpellucidum mass
ependymoma, intraventricular meningioma, subependymoma, choroid plexus papilloma, colloid cyst
intracerebral dermoid cyst can be thought of as being along a spectrum with ____ ___ at one end and _____ at the other

epidermoid cysts <--> teratomas

What is the tuber cinereum?

Hollow eminence of grey matter between mamillary bodies and optic chiasm.  It is just posterior to the pituitary stalk.  Part of the hypothalamus.

Hollow eminence of grey matter between mamillary bodies and optic chiasm. It is just posterior to the pituitary stalk. Part of the hypothalamus.

DDx of a cystic pituitary lesion

Craniopharyngioma (nodular and calcified), cystic pituitary adenoma (usually not cystic), Rathke cleft cyst.

What is this likely to be?

What is this likely to be?

gangioglioma

What is this lesion likely to be

What is this lesion likely to be

ganglioglioma

Define Behcet Disease

Multisystem vascular-inflammatory disease of unknown aetiology.

Describe Fabry disease

x-linked inherited lysosomal storage disease with a distinctive pattern of basal ganglia calcification.

Give a brief description of a Subependymoma

Asymptomatic 4th ventricle lesion/s found in older men.

DDx of an infiltrative brainstem lesion

brainstem glioma


brainstem encephalitis

Describe a typical ependymoma

4th ventricle lesion extending through the formamen of Luschka in a child with NF2

What is the Ddx for an ependymoma?

PNET-MB (medulloblastoma)


PA (pilocytic astrocytoma)


CPP (choroid plexus papilloma)

Benign but locally aggressive lesion arising from the sphenopalatine foramen and spreading laterally into the pterygopalatine fossa in children.

(Juvenile) nasopharyngeal angiofibroma

Lewy bodies are associated with

Lewy bodies are associated with

Parkinson disease

Pick bodies are associated with

Pick bodies are associated with

Frontotemporal lobar degeneration

Frontotemporal lobar degeneration may have what two patterns of tau deposition?

tangles and Pick bodies

Name two examples of "Parkinson-plus syndromes"

progressive supranuclear palsy


corticobasal degeneration

sporadic disorder characterized by alpha-synuclein cytoplasmic inclusions in oligodendrocytes

Multiple system atrophy

What protein is abundant in Lewy bodies?

alpha-synuclein

Huntington disease is characterized by degradation and atrophy of which neurones?

striatal neurones

Freidreich ataxia affects mainly the

spine

Ataxia-telangiectasia prognosis

death in late childhood

Amyotrophic lateral sclerosis usually presents in . .

late adulthood

Pneumonia due to reduced function of respiratory muscles is a complication of . .

Amytrophic lateral sclerosis

Results in death before age 3

Spinal muscular atrophy

Ataxia is characteristically the result of degeneration of which white matter circuit?

olivopontocerebellar

Parkinsonism is a result of degeneration of what white matter tract?

striatonigral tract

Vitamin B12 deficiency results in

Vitamin B12 deficiency results in

subacute combined degeneration of the spinal cord

neurenteric cyst

12 year old child, engulfed pituitary calcification

12 year old boy, engulfed pituitary calcification

germinoma

what is the hole called?

what is the hole called?

tentorial incisure

FLAIR shows subcortical hyperintensity in the region of the motor cortex.

FLAIR shows subcortical hyperintensity in the region of the motor cortex.

Amyotrophic lateral sclerosis.

the hummingbird sign is seen in

the hummingbird sign is seen in

Progressive supranuclear palsy

the hot-cross-bun sign is seen in

the hot-cross-bun sign is seen in

multiple system atrophy