Fetal Brain anomalies Flashcards

1
Q

Describe Hydranencephaly

A

-Its lethal -No cortex -Fluid filled cranium -Liquified brain due to vascular insult Work-up: -TORCH -Thrombophilia -R/O Renal dysplasia, heart defects -T13

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2
Q

Describe Porencephaly

A

One or more cystic cavities communicating with ventricles (associated with infarction to hemorrhage) Differs from arachnoid cyst because it is communicating with the ventricles

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3
Q

Describe Schizencephaly

A

Cleft connecting lateral ventricle to subarachnoid space (pia mater)

  • Absent cavum septum pellucidum
  • Developmental delay and seizures
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4
Q

Encephalocele

A

defect in skull allowing brain to protrude associated with Meckel Gruber

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5
Q

Lobar holoprosencephaly

A
  • presence of interhemipheric fissure and gyral continuity which is better seen on MRI
  • communication of ventricles across the midline
  • absent cavum septum pellucidum
  • fused fornix and frontal lobe
  • thalami is seperated

***hard to diagnose, the only finding is typically absent csp

***assess about diabetes

***associated with Smith-Lemli-Opitz and velocardio-facial syndrome

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6
Q

Semilobar holoprosencephaly

A
  • partial clevage of proseccephalon
  • absent CSP and incomplete interhemispheric fissure
  • fused frontal lobes but seperated occipital lobes
  • incomplete fusion of thalami
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7
Q

Alobar holoprosencephaly

A
  • single ventricle cerebrum (monoventricle)
  • no corpus callosum
  • fused thalami
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8
Q

Holoprosencephaly

A

Incomplete cleavage of the prosencephalon into left and right at 18th-28th day of gestation. Risk factors: DM, vitamin A exposure

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9
Q

Acrania-exencephaly/anencephaly

A

Acrania - flat bones in the cranial vault are either completely or partially absent

Excencephaly is the early manifestation of anencephaly

Anencephaly - a neural defect that occurs when the cephalic end of the neural tube fails to close usually between the 23rd and 26th days

Examine for diabetes

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10
Q

Agenesis of the corpus callosum

A
  • Caused by vascular event, genetic component, metabolic disorder, alcohol exposure
  • Starts to develop at 12 weeks and stops at 18 weeks -On ultrasound:

see absent CSP

rostral displacement of the roof of third ventricle

tear drop shaped ventricle

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11
Q

Arachnoid cyst

A

Benign non-communicating fluid collections within the arachnoid membrane. 80% normal development

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12
Q

Aneurysm of vein of Galen (cranium):

A

Midline cystic tubular structure posterior to the thalamus with blood flow . 55% - perinatal death rate. 15% alive with disability. 35% alive and normal.

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13
Q

What does the Rhombencephalon consist of:

A

It represents the hindbrain and consists of the medulla, pons and cerebellum. it appears as an anechoic structure in the first trimester, seen in the posterior part of the brain

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14
Q

What brain structures can be seen between 11 weeks and 13 weeks and 6 days?

A

Cranium

Frontal horn

Choroid plexus

Thalamus

Fourth ventricle

Brain stem

Intracranial lucency

Cisterna magna

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15
Q

What are the three axial planes which a fetal brain scan can be performed?

A

Transventricular

Transthalamic

Transcerebellar

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16
Q

What can be seen in the transventricular view?

A

This is the plane where the lateral ventricle is measured

17
Q

What can be seen at the transthalamic plane of the fetal brain

A

this is where BPD and HC can be obtained

18
Q

Fornix verses CSP

A

fornix is the line through the box where the csp is suppose to be. it is located inferior to the CSP

19
Q

What can you see at the transcerebellar plane?

A
20
Q

Amniotic band syndrome of the cranium:

A
21
Q

What does CMV look like in the fetal brain?

A

Look for interventricular synechiae

22
Q

Cavum veli interpositi cyst

A

if measuring more than 11mm then can be considered a cyst which is associated with ventriculomegaly

23
Q

Dural Sinus Thrombosis of the fetus

A
24
Q

Lissencephaly

A

absence of gyri and sulci

25
Q

Agenesis of corpus callosum

A

Widened interhemispheric space

Tear drop shaped ventricles (colpocephaly)

3rd ventricle is displaced upwards

26
Q

Absent CSP differential dx:

A
27
Q

Mega cisterna magna ddx:

A

Blakes pouch

Dandy walker malformation

28
Q

Blake’s pouch

A
29
Q

Septo-Optic Dysplasia:

A
  • absent cavum septi pellucidi
  • frontal horns communicating
  • the fornix is not fused
  • in coronal view: frontal horn is square shape at the points and the whole thing comes to a point inferiorly indicating seperated fornices
  • the optic chiasm is small

(hypothalamic hypopituitarism, delay)

30
Q

Syntelencephaly:

A
  • it is a variant of holoprosencephaly
  • fusion of the posterior portion of the frontal and parietal lobes across the midline
  • absent cavum septi pellucidi