Head and Neck Flashcards

(58 cards)

1
Q

resolution of aphthous ulcers

A

spontaneously in 7-10 days

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2
Q

clinical forms of candidiasis

A

pseudomembranous aka thrush
hyperplastic
erythematous

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3
Q

hairy leukoplakia

A

lateral border
cannot be scraped off
associated with EBV

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4
Q

cause of precancerous lesions

A

tobacco

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5
Q

most common lesion of head and neck

A

squamous cell carcinoma

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6
Q

HPV associated with sinonasal papilloma

A

6 and 11

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7
Q

virus nasopharyngeal carcinoma

A

EBV

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8
Q

presentation nasopharyngeal carcinoma

A

nasal obstruction and epistaxis

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9
Q

ostosclerosis

A

bilateral hearing loss

abnormal middle ear bone deposition

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10
Q

treatment of most head and neck neoplasms

A

excision

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11
Q

paraganglioma

A

clusters of neuroendocrine cells

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12
Q

components of pleomorphic adenoma

A

mixed-epithelial and myoepithelial

benign and painless tumor

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13
Q

location of warthin tumor

A

restricted to parotid gland

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14
Q

mucoepidermoid carcinoma

A

most common malignant tumor

t(11;19)(q21;p13)

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15
Q

adenoid cystic carcinoma

A

perineural invasion
PAINFUL MASS
parotid and submandibular glands

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16
Q

location of thyroglossal duct cyst

A

most common

midline

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17
Q

course of thyroglossal duct cyst

A

asymptomatic until infected
painless midline swelling
moves with swallowing or sticking out tongue
can be associated with ectopic thyroid

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18
Q

embryology causing thyroglossal duct cyst

A

connects thyroid and foramen cecum
at 5th week fragments, mesoderm condenses into hyoid bone
atrophies by end of 8th week

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19
Q

characteristics of thyroglossal duct cyst

A

epithelial lined cyst
from failure of normal obliteration
infrahyoid most common

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20
Q

imaging of thyroglossal duct cyst

A

ultrasound to diagnose
CT may be used
treat with surgical resection

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21
Q

origin of dermoid

A

outer layers of skin do not properly grow together

lined with epithelium, contains hair, sebaceous glands, sweat glands

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22
Q

characteristics of dermoid

A

moves independently with skin

doughy

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23
Q

origin of branchial cleft cyst

A

remnants of embryonic development from failure of obliteration of one of the branchial clefts
epithelial lined cyst

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24
Q

location branchial cleft cyst

25
cyst
no external or internal opening
26
sinus
internal or external opening
27
fistula
both internal and external openings
28
first branchial cleft cyst
type 2 more common type 1 duplication of auditory canal type 2 at angle of mandible
29
most common branchial cleft cyst
second
30
characteristics of second branchial cleft cyst
inferior to mandible and anterior to SCM sinus or fistula tract can extend to ipsi tonsil
31
third branchial cleft cyst
anterior to SCM lower in neck end in pharynx at thyrohyoid member often presents with lower neck infection L>R
32
characteristics of cystic hygroma
lymphatic malformation | multi-loculated lesion in left posterior triangle
33
presentation of cystic hygroma
soft, painless, doughy mass may transilluminate evaluate for tracheal deviation or evidence of impending airway obstruction
34
hemangiomas
usually not present at birth | bright red macule or papule rash with clear boundaries
35
liver MRI and hemangiomas
if 5 or more cutaneous
36
proliferative phase of hemangiomas
continues for up to 15 to 18 months reach 85% of size by 5 months of age may ulcerate
37
involutional phase of hemangiomas
superficial lesions change to dull red, then gray flatten and soften most complete by 10 yo
38
subglottic hemangioma
high risk with segmental beard distribution-preauricular, chin, lower lip, neck biphasic stridor initially diagnosed as croup
39
hemangiomas on MRI
gadolinium MRI study of choice well circumscribed, lobulated mass salt and pepper pattern dilated vessels
40
indications to intervene for hemangiomas
``` accelerated growth hemorrhage infection ulceration problems breathing, swallowing high output CHF ```
41
pharmacological treatment of hemangiomas
propranolol
42
congenital torticollis
SCM is tight and shortened usually discovered in first 6-8 weeks of life injury causes scarring that leaves it tight associated with hip dysplasia
43
presentation torticollis
tilted in a laterally, bending toward affected muscle | rotate to opposite side
44
concerning lymphadenopathy
``` generalized occipital, auricular, supraclavicular, mediastinal, epitrochlear, posterior cervical nodes firm matted nontender >2cm systemic symptoms ```
45
biopsy LN
supraclavicular | 2-6 weeks, >3cm, not responding to antibiotics or risk factors for malignancy
46
common cause of lymphadenopathy
viral most common
47
MAI lymphadenopathy
submandibular common firm, painless mass that does not respond to antibiotics may enlarge and become fluctuant violaceous hue
48
treatment MAI
macrolides-azithromycin also rifampin, ethambutol, aminoglycosides, or fluroquinolones treated with 3 antimicrobials for 12 months excision but not incision and drainage
49
cat scratch disease
bartonella primary inoculation at lesion self limited 6-12 weeks treat with doxy, erythro, azithro
50
Kawasaki disease
``` fever >5 days cervical lymphadenopathy edema/eryhtema palms and soles conjunctivitis strawberry tongue ```
51
most common neoplasm causing lymphadenopathy in children
lymphoma
52
lymphoma
painless neck mass hodgkin in adolescents; non-hodgkin in 2-12 yo M>F hodgkin from EBV
53
concern for lymphoma
>3cm and firm multiple regions supraclavicular or posterior triangle location
54
rhabdomyosarcoma
arise from soft tissue-skeletal muscle
55
embryonal rhabdomyosarcoma
head and neck or GU
56
alveolar rhabdomyosarcoma
arms, legs, chest, abdomen, genital organs or anal area
57
anaplastic rhabdomyosarcoma
rare in children
58
presentation rhabdomyosarcoma
depend on location | commonly a lump or swelling that keeps getting bigger