Brooke's Flashcards

1
Q

What is hyperdense on CT?

A

Hyperdense=bright on CT

Blood and calcifications

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2
Q

What is hypodense on CT?

A

Hypodense=dark on CT compared to surrounding brain.

Could be infarction, edema, pneumocephalus.

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3
Q

Pneumonic for an emergent CT head.

A

Blood Can Be Very Bad

  1. Blood - look for epidural/subdural hematomas, ICH, IVH, subarachnoid hemorrhage and (also) extracranial hemorrhage.
  2. Cisterns - look for the presence of blood, effacement and asymmetry in four key cisterns (perimesencephalic, suprasellar, quadrigeminal and Sylvian cisterns).
  3. Brain - look for asymmetry or effacement of the sulcal pattern, gray-white matter differentiation, structural shifts and abnormal hypodensities (e.g. air, edema, fat) or hyperdensities (e.g. blood, calcification).
  4. Ventricles - look for intraventricular hemorrhage, ventricular effacement or shift and for hydrocephalus.
  5. Bone - look for skull fractures (especially basal) on bone windows (soft tissue swelling, mastoid air cells and paranasal sinuses fluid in the setting of trauma should raise the possibility of a skull fracture; intracranial air means that the skull and the dura have been violated somewhere).
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4
Q

Things that are bright on FLAIR imaging?

A
  1. Acute SAH.
  2. Edema.
  3. Acute infarcts.

There are others but those are the big ones.

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5
Q

When does the anterior fontanelle normally close?

A
  1. 4-26 months of age.
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6
Q

When does the posterior fontanelle normally close?

A
  1. Before 2 months of age.
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7
Q

An enlarged posterior fontanelle can occur in what conditions?

A
  1. Congenital hypothyroidism.
  2. Trisomy syndromes.
  3. Rickets.
  4. Osteogenesis imperfecta.
  5. Hydrocephalus.
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8
Q

A depressed anterior fontanelle can be a sign of what condition?

A
  1. Dehydration.
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9
Q

When does the embryonic skull begin to form?

A
  1. Between the 23rd and 26th day of gestation.
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10
Q

What is thought to initiate cranial suture formation?

A
  1. Osteogenic fronts, which consist of osteoprogenitor cells and osteoblasts at the leading edges of developing bone.
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11
Q

What factors determine normal suture formation?

A
  1. Bone deposition by osteoblasts.
  2. Bone remodeling by osteoclasts.
  3. Apoptosis in the frontal boundaries.
  4. Local interactions between dura mata and the sutures.
  5. Growth factors (fibroblast growth factor receptor and transforming growth factor).
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12
Q

True or false: The primary influence for cranial growth is the growing brain.

A

True.

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13
Q

Name the sutures of the cranium.

A
  1. Metopic (between both frontal bones).
  2. Sagittal (between both parietal bones).
  3. Two coronal (between parietal and frontal bones).
  4. Two lambdoid (between occipital and parietal bones).
  5. Squamosal (between parietal, temporal, and sphenoid bones).
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14
Q

Which of the sutures naturally closes earliest?

A
  1. Metopic suture - usually closed by 9 months of age.
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15
Q

What are the 4 principles associated with suture closing?

A
  1. Calvarial bones directly next to the fused suture act as a single bone plate with decreased growth potential.
  2. Asymmetrical bone deposition occurs at the sutures along the perimeter of the bone plate with increased bone deposition at the outer margin.
  3. Nonperimeter sutures in line with the fused suture deposit bone symmetrically at their suture edges.
  4. Perimeter sutures adjacent to the fused suture compensate to a greater degree than the other distant sutures.
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16
Q

What clinically similar condition must be differentiated from true craniosynostosis?

A
  1. Deformational plagiocephaly, which is more common than craniosynostosis and results from external forces causing skull deformation into a parallelogram shape.
17
Q

What types of craniosynostosis resemble deformational plagiocephaly?

A
  1. Unilateral coronal and lambdoid craniosynostosis.
18
Q

What is scaphocephaly?

A
  1. Craniosynostosis caused by sagittal suture closure.
19
Q

What is frontal plagiocephaly?

A
  1. Craniosynostosis caused by unilateral coronal suture closure.
20
Q

What is trigonocephaly?

A
  1. Craniosynostosis caused by metopic suture closure.
21
Q

What is posterior plagiocephaly?

A
  1. Craniosynostosis caused by unilateral lambdoid closure.
22
Q

What is brachycephaly?

A
  1. Craniosynostosis caused by bilateral lambdoid suture closures.
23
Q

True or false: Sagittal craniosynostosis is the most common form.

A
  1. True - accounts for 40-60% of all craniosynostosis cases.
24
Q

How does the head look in sagittal synostosis?

A
  1. AP elongation with frontal and/or occipital bossing and biparietal and bitemporal narrowing (long, skinny head).
25
Q

How does the head look in unilateral coronal synostosis?

A
  1. Flattened ipsilateral forehead and parietal area, compensatory contralateral frontal bossing and ipsilateral temporal bulging.
  2. Nasal root deviation to ipsilateral side.
  3. Anterior displacement of ipsilateral ear.
  4. Superiorly displaced sphenoid wing –> heightened orbit (Harlequin eye).
26
Q

How does the head look in bilateral coronal synostosis?

A
  1. Flattened occiput and forehead, anterior displacement of the skull vertex, widening of the upper face, prominent globes from decreased AP diameter (basically a short, wide head).
27
Q

How does the head look in metopic synostosis?

A
  1. Trigonocephaly - fonrtal keel, narrowed bitemporal width, anterior displacement of coronal suture, retrusion of orbital rims, reduced frontonasal angle.
28
Q

True or false: Lambdoid synostosis is the rarest of the nonsyndromic craniosynostoses?

A
  1. True - lambdoid synostosis accounts for 2-3%.
29
Q

How does the head look in lambdoid synostosis?

A
  1. Unilateral occipitoparietal flattening.
  2. Contralateral posterior bossing.
  3. Prominent occipitomastoid bulge.
  4. Posterior and inferior displacement of ear.
  5. Trapezoid shape when seen from above.
30
Q

Craniosynostosis patients are at risk for increased ICPs. What is the mechanism?

A
  1. Distorted subarachnoid spaces lead to changes in CSF circulation.
31
Q

What are arachnoid cysts composed of?

A
  1. CSF-like fluid surrounded by an arachnoidal membranous wall.
32
Q

Why do arachnoid cysts form?

A
  1. Abnormal CSF flow during development causes cyst formation.
33
Q

Where are arachnoid cysts most commonly located?

A
  1. Sylvian fissure and middle fossa.
34
Q

What are other locations of arachnoid cysts other than the Sylvian fissure?

A
  1. Cerebellopontine angle.
  2. Quadrigeminal cistern.
  3. Sellar and suprasellar areas.
35
Q

True or false: arachnoid cysts have high malignant potential?

A
  1. False, most are asymptomatic and benign.
36
Q

What are the main surgical options for treatment of arachnoid cysts?

A
  1. Cyst shunting.
  2. Open fenestration.
  3. Endoscopic fenestration.

Most won’t need any type of surgical intervention!