Fetal Spine Part 1 Flashcards

1
Q

When scanning the fetal spine, what is very important to see?

A

intact skin line

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2
Q

Most congenital spinal problems are the result of defective closer of the neural tube during what week of embryonic development?

A

4th

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3
Q

Neural tube defects are associated with elevated ______.

A

AFP

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4
Q

Spinal dysraphism is a broad term given to a group of anomalies related to:

A

any abnormalities of the dorsum of the embryo
or
neurological disorders related to malformations of spinal cord (NTD fall under this group)

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5
Q

Spinal dysraphism can be divided into 2 pathological entities:

A

open spinal dysraphism

closed spinal dysraphism

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6
Q

What are examples of open spinal dysraphism?

A

meningocele

myelomenigocele

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7
Q

What are examples of closed spinal dysraphism?

A
spinal dermal sinus
lipomyelomenigocele
diastematomyelia
neurentric cysts
thickened filum terminale
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8
Q

What is spinal dermal sinus

A

an epithelium-lined tract from the skin to the spinal cord, cauda equina or arachnoid

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9
Q

What is lipomyelomeningocele

A

usually presents as a subcutaneous fatty mass just above the intergluteal cleft

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10
Q

What is diastematomyelia

A

split cord malformation

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11
Q

What is neurentric cysts

A

type of foregut duplication cyst, associated either with vertebral or CNS abnormalities
most commonly occur in thoracic region

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12
Q

Tight filum terminale syndrome is associated with what?

A

vertebral body deformities and spina bifida

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13
Q

Tight filum terminale syndrome:

A

incomplete involution to distal spinal cord

results in neurological deficiencies, pain, bowel dysfunction

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14
Q

What will be seen sonographically for tight filum terminale syndrome?

A

abnormally thickened filum terminale

sometimes with cysts/lipoma

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15
Q

For tight filum terminale syndrome, the diameter of the filum terminale should not exceed:

A

2mm

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16
Q

Tethered spinal cord is

A

attached to surrounding tissue

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17
Q

Neural tube defects involving ___________ _______ are referred to as

A

vertebral arches, spina bifida

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18
Q

What is common to all types of spina bifida?

A

non-fusion of the embryonic halves of the vertebral arches

19
Q

The majority of spina bifida occurs where?

A

lumbosacral region

20
Q

Severe spina bifida involves the

A

spinal cord

21
Q

What is the most severe form of spina bifida

A

myelomenigocele

22
Q

What is the mildest form of SB

A

occulta

one or more vertebrae are malformed and covered with skin

23
Q

Many children with SB also have

A

hydrocephalus

24
Q

What’s the difference between open and closed SB?

A

closed is covered by skin, open is not

25
Q

Meningocele

A

meningeal membrane and CSF protrude through defect in vertebral arch (skin is mostly intact)

26
Q

Myelomeningocele

A

meningeal membrane, CSF, and neural tissue (spinal cord) protrude through defect (skin partly covers defect)

27
Q

Myeloschisis and rachischisis are often interchangable terms. True or false

A

True

28
Q

Myeloschisis

A

open, flattened spinal cord, exposed through a wide defect in the posterior neural arch and defect in musculature and skin (no skin or meningeal covering)

29
Q

Rachischisis

A

complete SB. cleft through entire spine from cervical to sacral region- open, flattened spinal cord (entire spinal cord is exposed)

30
Q

SB occulta (or closed)

A

minor and insignificant abnormality
no clinical symptoms
rarely diagnosed prenatally

31
Q

What are indications of SB occult?

A

dimple, tuft of hair or red mark on the back

32
Q

Most spina bifida cases are what classification? How much?

A

Open – 80%

33
Q

What type of spina bifida is most common?

A

Myelomeningocele (also most severe.. myeloschisis is most severe form of myelomeningocele)

34
Q

Spina Bifida Aperta– Cystica involves

A

protrusion of the meninges and spinal cord through the defect in the posterior vertebral arch

35
Q

If a mass contains only meninges with CSF, the anomaly is called

A

SB w/ meningocele.

spinal cord and roots are in their normal position, but there may be spinal cord anomalies

36
Q

Meninges protrude _____ _____ _____ through the cleft in the malformed _________ _________.

A

under the skin, vertebral arch

37
Q

Spina bifida apeta- cystica. If the spinal cord and/or nerve roots protrude in the mass, the defect is called

A

SB w/ myelomeningocele

38
Q

What’s the most severe form of myelomeningocele?

A

myeloschisis

39
Q

The more ______ the level of defect, the more severe the associated nerve dysfunction and paralysis may be.

A

cranial

40
Q

There is a small skin layer covering the nerve tissue with myeloschisis. True or false

A

False- the nerve tissue is fully bare and a dermal or meningeal covering is absent

41
Q

Many individuals with SB have an associated abnormality of the cerebellum, called:

A

Arnold Chiari II malformation

42
Q

The cerebellum is larger in those individuals with SB. True or false.

A

False- cerebellum is smaller, especially those with higher lesion levels

43
Q

What is abnormally developed in individuals with spina bifida myelomeningocele? What percentage?

A

corpus callosum

70-90%

44
Q

What are some sonographic signs of spina bifida seen in the head?

A
nonvisualization of cisterna magna
deformation of cerebellum (banana sign)
concave frontal bones (lemon sign)
dilation of lateral ventricles
Chiari II malformation (97%)
BPD lower than expected