Normal fetal Brain Flashcards

1
Q

Echogenic area located with in the atria of lateral veins bilaterally

A

Choroid plexus

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2
Q

Located posterior portion of brain

should not exceed 10 mm

A

Lateral vents

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3
Q
  • Located in posterior portion of brain
  • can be used to estimate GA up to 20 weeks
  • Measurement not accurate after 30 weeks
A

Cerebellum

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4
Q

Seen on sono after 30 weeks

A

Epiphyseal centered of bones (femur)

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5
Q

o Anechoic area in posterior brain

o Should not exceed 10mm

A

Cistern Magna (posterior fossa)

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6
Q

o Should be < 6 mm
o Not accurate after 21 weeks
o Measured outer edge to outer edge

A

Nuchal fold

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7
Q

-)= Lateral vents > 10mm
• posterior lateral ventricular atria 1st place to enlarge due to ↑ CSF
• Often assoc. w/ other abnormalities
Classifications:
1. Aqueductal stenosis- caused by narrowing of 3rd ventricle outflow (Aqueduct of Sylvius)
2. Communicating hydrocephalus- dilation of all ventricles
3. Dandy Walker Malformation-
SONO: dilated ventricles, dangling choroid, POLY, fetal ascites and hepatomegaly

A

Ventriculomegaly (hydrocephaly)

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8
Q
  • Splaying of the cerebral vermis, communicating w/ a dilated 4th ventricle
  • Increased cisterna magna >10mm
  • Ventriculomegaly
  • Assoc. w/ other abnormalities and possible agenesis of corpus callosum
A

Dandy walker syndrome

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9
Q
  • Can be complete or partial and assoc w/ other anomaly
  • Cannot be diagnosed until after 18weeks
  • Absence of cavum septum pellucidum
  • “tear drop ventricles” Enlargement of posterior horn of lateral vents but not anterior
  • 3rd ventricle enlarged and displaced superiorly
A

Agencies of corpus callous

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10
Q
  • Means- “water no brain”
  • Absence of cerebral hemispheres w/ normal developed meninges and skull due to occlusion of ICA
  • Cerebral cortex replaced by fluid causing macrocephaly and POLY
  • Thalami, brain stem and cerebellum are spared
A

Hydrancephaly

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11
Q

“the face predicts the brain”
• Cranial vault is formed BUT has a single large midline ventricle
• Most often assoc. w/ TRISOMY 13

-Alobar, semi lobar,lobar

A

Holoprosencephaly (3 classifications)

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12
Q

Most severe
Large single cavity, fused thalami, absent 3rd ventricle and falx
Facial anomalies and hypotelorism

A

Alobar

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13
Q

partial separation of hemispheres and lateral vents

Cleft palate and lip

A

Semilobar

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14
Q

interhemisphere fissure developed except fused anterior horns of LV, and absent CSP

A

Lobar

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15
Q
  • Cystic areas with cerebral parenchyma

* Caused from cranial bleeds

A

Porencephaly

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16
Q
  • Rare malformation of abnormal clefts in cerebral hemisphere
  • Usually bilateral the brain appears, “split”
A

Schizencephaly

17
Q

small head circumference below 3 standard deviations of normal

A

Microcephaly

18
Q
  • Can be unilateral, bilateral, multiple or single, small or large
  • Can be assoc w/ Trisomy 18 or 21 if other findings are present
  • Resolve by 28 weeks / 3rd trimester
A

Choroid plexus cyst

19
Q
  • BENIGN, anomaly, MC occurs in posterior neck
  • Sac filled w/ lymphatic fluid due to obstruction
  • Assoc. w/ DOWNS syndrome or TURNERS syndrome
  • Can be assoc. w/ fetal hydrops and ascites
A

Cystic hygroma

20
Q
  • “lateral cleft lip” is commonly isolated
  • “medial cleft lip, assoc w/ chromosomal abnormalities”
  • Possible, POLY bc they cant swallow properly
A

Cleft lip/Plate

21
Q
  • A teratoma arising from the oral cavity or pharynx (soft palate, tongue or jaw)
  • Assoc. w/ POLY
A

Epignathus

22
Q
  • Complex, solid, cystic tumor seen near the fetal neck

* Spine will be normal

A

Cervical teratoma

23
Q
  • Increased soft tissue thickness over the posterior aspect of the neck
  • > 6mm is abnormal measured between 15-21weeks
  • Assoc w/ chromosomal syndromes especially Trisomy 21
  • Normal nuchal fold should be <6mm ** ON TEST **

A

Nuchal thickening