NB2 10+11 Flashcards

1
Q

Clefts

A

can occur on its own or part of a syndrome

usually multifactorial

can be anterior or posterior

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2
Q

clefts of the anterior palate

A

Anterior to the incisive fossa

Results from failure of the fused lateral palatine processes (secondary palate) to meet and fuse with the primary palate

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3
Q

clefts of the posterior palate

A

posterior to the incisive fossa

Results from failure of the lateral palatine processes to meet and fuse with each other and the nasal septum

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4
Q

cleft of the anterior and posterior palate

A

Results from failure of the lateral palatine processes to meet and fuse with the primary palate, with each other, and the nasal septum

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5
Q

cleft lip

A

Cleft lip can occur independently from underlying bony deformities

can be unilateral or multilateral

Failure of maxillary prominence to fuse with the fused medial nasal prominence(intermaxillary segment) on one or both sides

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6
Q

Unilateral Cleft Upper Lip

A

Failure of fusion of left maxillary prominence with the fused medial nasal prominences (intermaxillary segment)

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7
Q

Bilateral Cleft Upper Lip

A

Failure of both maxillary prominences to fuse with the intermaxillary segment

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8
Q

Median Cleft Upper Lip

A

Failure of fusion of the two medial nasal
prominences to form the intermaxillary segment

usually seen with other morphologies

rare

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9
Q

Median Cleft Lower Lip

A

rare

Failure of fusion of the mesenchyme of the
mandibular prominences

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10
Q

Oblique Facial Cleft

A

Failure of maxillary prominence to fuse with lateral nasal prominence

Nasolacrimal duct is visible

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11
Q

First arch syndrome - Treacher Collins Syndrome

A

failure of NCS migration into the first arch

underdeveloped jaw (micrognathia) 
cleft palate (50%) 
conductive hearing loss
pinna malformation 
drooping eyelid (lower)
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12
Q

First arch syndrome - Pierre Robin Sequence

A
  1. Micrognathia or retrognathia
  2. glossoptosis (retraction of tongue)
  3. cleft palate
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13
Q

cervical (branchial) sinus

internal and external??

A

external:
Open externally along ant. border of SCM

Failure of the second pharyngeal groove and cervical sinus to obliterate

internal:
Opens internally into the tonsillar fossa or near the palatopharyngeal arch

Most result from persistence of the proximal part of the
second pouch (more rare)
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14
Q

CERVICAL (BRANCHIAL) FISTULA

A

Persistence of the 2nd pouch and cervical sinus

Abnormal tract passing between external and
internal carotid arteries

opening on the side of neck externally & in the
tonsillar sinus internally.

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15
Q

cervical (branchial) cysts

A

persistence of parts of cervical sinus and /or 2nd pharyngeal groove with no internal or external communication

Cystic swelling along anterior border of the sternocleidomastoid

slowly will enlarge with fluid and cells
painless
late childhood

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16
Q

Thyroglossal Duct Cyst and Sinus

A

Cystic remnant of the thyroglossal duct

usually in the midline

may develop anywhere along the pathway of the duct

painless, enlarging, movable

Infection can cause perforation unto to skin of the neck leading to development of a thyroglossal duct sinus

17
Q

Craniopharyngiomas

A

usually benign and sometimes functional tumors may develop from minor epithelial remnants of the hypophyseal diverticulum

18
Q

parathyroid anomalies

A

Supernumerary parathyroid glands – early
division of the primordium of the gland

Absence of the parathyroid gland – atrophy or
failure of differentiation of the primordium

Ectopic parathyroid glands – usually within the
thyroid gland or thymus