CNS Flashcards

1
Q

The following are true about neurons, except:

a. highly metabolically active
b. proliferates after an injury
c. lengthy lifespan
d. high metabolic rate

A

B

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2
Q

The following are seen during axonal reaction, except:

a. enlargement and rounding up of cell body
b. central displacement of nucleus
c. enlargement of nucleolus
d. dispersion of Nissl substance

A

B

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3
Q

It is the most common histopathologic marker of CNS injury

a. gliosis
b. reactive astrocytes
c. genitocyric astrocytes
d. rosenthral fibers

A

A

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4
Q

The following causes neural tube defects due to primary bony defects caused by abnormal axial mesoderm, except:

a. encephalocele
b. meningocele
c. spina bifida
d. myelomeningocele

A

D

failure of neural tube closure: anencephaly, myelomengingocele

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5
Q

It is the most common neural tube defect

a. encephalocele
b. meningocele
c. spina bifida
d. myelomeningocele

A

C

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6
Q

It is the hypoplasia of cerebellar dermis with apparent elongation of cerebellar peduncles and altered shape of brainstem

a. Chiari type II malformation
b. Chiari type I malformation
c. Dandy-Wlaker malformation
d. Joubert syndrome

A

D

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7
Q

It is the most common type of intracranial aneurysm

a. mycotic
b. traumatic
c. saccular
d. dissecting
e. atherosclerotic

A

C

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8
Q

It is the common causative irganism of acute pyogenic meningitis in young adults

a. E. coli
b. group B strep
c. N. meningitidis
d. S. pneumoniae
e. L. monocytogenes

A

C

a and b - infants
d and e - older adults

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9
Q

Inflammation of meninges and brain parenchyma

a. meningitis
b. meningoencephalitis
c. brain abscess
d. extradural abscess

A

B

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10
Q

Commonly associated with osteomyelitis

a. meningitis
b. meningoencephalitis
c. brain abscess
d. extradural abscess

A

D

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11
Q

Most common prion disease that manifests as rapidly progressive dementia

a. Creutzfeldt-Jakob disease
b. Alzheimer disease
c. Germann-Straussler-Sheinker syndrome
d. fatal familial insomnia

A

A

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12
Q

Pick bodies

a. Parkinson disease
b. Alzheimer’s disease
c. Huntington disease
d. Frontotemporal lobar degenerations

A

D

Parkinson - lewy bodies

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13
Q

Autosomal recessive, ataxic-dyskinetic syndrome beginning in childhood

a. spinocerebellar ataxia
b. Friedreich ataxia
c. Ataxia-telangiectasia
d. ALS

A

C

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14
Q

Which of the following is WHO grade I tumor?

a. pilocytic astrocytomas
b. diffuse astrocytoma
c. anaplastic astrocytoma
d. gliobastoma

A

A

Grades I-IV: PDAG

infiltrating: WHO grade II-IV

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15
Q

Have best prognosis among glial tumors

a. astrocytoma
b. ependymoma
c. oligodendroglioma
d. subependymoma

A

C

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