Fetal Spine Part 1 Flashcards

(44 cards)

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

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
Meningocele
meningeal membrane and CSF protrude through defect in vertebral arch (skin is mostly intact)
26
Myelomeningocele
meningeal membrane, CSF, and neural tissue (spinal cord) protrude through defect (skin partly covers defect)
27
Myeloschisis and rachischisis are often interchangable terms. True or false
True
28
Myeloschisis
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
Rachischisis
complete SB. cleft through entire spine from cervical to sacral region- open, flattened spinal cord (entire spinal cord is exposed)
30
SB occulta (or closed)
minor and insignificant abnormality no clinical symptoms rarely diagnosed prenatally
31
What are indications of SB occult?
dimple, tuft of hair or red mark on the back
32
Most spina bifida cases are what classification? How much?
Open -- 80%
33
What type of spina bifida is most common?
Myelomeningocele (also most severe.. myeloschisis is most severe form of myelomeningocele)
34
Spina Bifida Aperta-- Cystica involves
protrusion of the meninges and spinal cord through the defect in the posterior vertebral arch
35
If a mass contains only meninges with CSF, the anomaly is called
SB w/ meningocele. | spinal cord and roots are in their normal position, but there may be spinal cord anomalies
36
Meninges protrude _____ _____ _____ through the cleft in the malformed _________ _________.
under the skin, vertebral arch
37
Spina bifida apeta- cystica. If the spinal cord and/or nerve roots protrude in the mass, the defect is called
SB w/ myelomeningocele
38
What's the most severe form of myelomeningocele?
myeloschisis
39
The more ______ the level of defect, the more severe the associated nerve dysfunction and paralysis may be.
cranial
40
There is a small skin layer covering the nerve tissue with myeloschisis. True or false
False- the nerve tissue is fully bare and a dermal or meningeal covering is absent
41
Many individuals with SB have an associated abnormality of the cerebellum, called:
Arnold Chiari II malformation
42
The cerebellum is larger in those individuals with SB. True or false.
False- cerebellum is smaller, especially those with higher lesion levels
43
What is abnormally developed in individuals with spina bifida myelomeningocele? What percentage?
corpus callosum | 70-90%
44
What are some sonographic signs of spina bifida seen in the head?
``` 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 ```