Fetal Spine (lesson 22) Flashcards

1
Q

When can you visualize the 3 ossifications of the spine in TRV plane?

A

16th weeks

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2
Q

Where do the two posterior spine ossifications lie?

A

In the laminae

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3
Q

The anterior ossification lies within which part of the spine?

A

vertebral body

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4
Q

Where does the conus medullaris image in the second and third trimester?

A

L2, L3

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5
Q

What are the 3 determinations of spinal normalcy?

A
  • intact neural canal
  • normal location and shape of spinal ossification centers
  • intact dorsal skin contour
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6
Q

When will you see a higher level of AFP?

A

During structural defects, such as anencephaly or spina bifida

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7
Q

How long is the process of the neural tube formation?

A

2 days, cannot be disrupted or bad stuff happens

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8
Q

What are the two types of spina bidifa defects?

A

Ventral defect and dorsal defect

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9
Q

What is a ventral defect for spina bifida?

A

Vertebral body splitting and a neurogenic-origin cystic structure, happens higher in the spine

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10
Q

What is a dorsal defect for spina bifida?

A

Subdivisions of open and closed forms (defect not covered by skin - open; defect covered by skin - closed)

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11
Q

Closed spina bifida is also known as?

A

Spina bifida occulta

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12
Q

What is spina bifida occulta?

A

This type of spina bifida has a skin covering and is not noticeable on the surface, except for a small dimple or tuft of hair; usually a finding without consequence. Often at the sacrolumbar version.

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13
Q

What is spina bifida aperta?

A

Open spina bifida, a full thickness defect of the skin, underlying soft tissue and vertebral arches which exposes the neural canal

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14
Q

What (3 factors) plays a definitive role in causes of NTD?

A

genetic factors, environmental factors, nutritional factors

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15
Q

Second trimester hydrocephalus occurs ALL THE TIME in what?

A

Neonates with spina bifida aperta

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16
Q

What does the appearance of a normal cerebellum and cisterna magna exlude?

A

Myelomeningocele

17
Q

What sort of abnormality is the combination of lateral and anterior curvature?

A

Kyphoscoliosis

18
Q

What is a lateral displacement of the atnerior ossification center?

A

Scioliosis

19
Q

What is caudal regression syndrome?

A

A heterogeneous group of congenital anomlaies affecting the caudal spine and spinal cord, the hindgut, the UG system, and the lower limbs

20
Q

What is the sonographic appearance of Caudal Regression Syndrome?

A

SAG and TRV views of spine uncover vertebral absence, fused iliac wings, decreased femoral head distance, short femurs, and club feet

21
Q

Where is the most common location for a teratoma in the fetus?

A

Sacrococcygeal (caudal end)

22
Q

What is the most common neoplasm in the newborn?

A

Teratoma

23
Q

Do sacrococcygeal teratomas happen more frequently in male or females?

A

Females

24
Q

What does a Sacrococcygeal Termatoma look like on US?

A

The tumor mass images as a protrusion between the anus and coccyx, may be solid or complex

25
Q

Where does the cystic component of a sacrococcygeal teratoma come from?

A

Choroid plexus tissue secretes cerebrospinal fluid

26
Q

What prenatal risks (2) come from sacrococcygeal teratomas?

A

Congestive heart failure and hydrops

27
Q

Perinatal mortality and morbidity are most strongly related to which?

A

Cardiac failure, subsequent fetal hydrops, polyhydramnios, and preterm delivery