198 Differential Diagnosis of Neck Masses Flashcards

1
Q

Major categories of neck masses in children:

A

Congenital - Cysts

AcquIred - Infectious

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2
Q

Branchial cleft cyst forerunner

A

2nd/3rd branchial

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3
Q

Hemangioma involution period

A

18-24 mos

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4
Q

Most common neck malignancy in children

A

Lymphoma

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5
Q

Most common locations , malignant neck lesions

A

Posterior cervical or supraclavicular

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6
Q

Any node that falls outside this cutoff size - outside the range of typical lymphoid hyperplasia

A

2 cm in diameter

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7
Q

Branchial cleft cysts - common locations

A

First branchial - near angle of mandible
2nd - deep to anterior border of SCM
3rd - near upper pole of thyroid

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8
Q

Modalities to differentiate TGDC from ectopic thyroid

A

Thyroid US

Radionuclide scanning

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9
Q

Agents in treating macrocystic lesions

A

Alcohol
OK 432
doxycycline

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10
Q

Most common location of laryngeal hemangioma

A

Subglottic larynx

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11
Q

Medical therapy for hemangioma

A

Propranolol

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12
Q

CT or MRI finding - teratoma - that may assist in diagnsosi

A

Instrinsic calcifications

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13
Q

Dermoid cyst locations

A

Orbit
Nose
NP
Oral cav

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14
Q

Usual location fo dermoid cyst

A

Midline, sumental

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15
Q

Structure defining if laryngocele is internal or external

A

Thyroid cartiage
If within - internal
Extends beyond in ceohalad to protrude through thyrohyoid membrane - external

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16
Q

Vascular mal:

Slow flow lesions:
Fast flow lesions:

A

Slow: capillary malformation, venous mal

Fast: arterial, AV mal

17
Q

Most common causative organisms of suppuration in neck

A

S. Aureus

GABS

18
Q

Mumps manifestations

A

Orchitis
Meningitis
Sensorineural HL

19
Q

Kawasaki criteria

A

CLAD, acute, non purulent, usually unilateral

Erythema, edema, desquamation of hands and feet

Polymorphous exanthem

Bilateral painless conjunctival infection

Erythema and infection of lips and oral cavity

20
Q

Sub acute stage, kawasaki, clinical sequelae in 15-20%

A

Coronary artery aneurysms

21
Q

NHL extralmphatic sites of involvement

A

Liver, lung, bone marrow

22
Q

Rhabdomyosarcoma types

A

Embryonal (Most common)
Alveolar
Pleomorphic

23
Q

Peak ages of rhabdomyosarcoma

A

2-5 years old

15-19 years old

24
Q

Syndrome associated with Neuroblastoma

A

Horner syndrome (ipsilateral)

25
Q

60% of malignant epithelial neoplasm histology

A

Mucoep

Acinic cell