Soft Tissue Flashcards

1
Q

Reactive Process; due to chronic irritation or trauma; commonly along the occlusal plane of the buccal mucosa; well-circumscribed, slowly growing, polyp; firm or spongy; may be ulcerated; fixed to mucosa; asymptomatic

A

Irritation fibroma

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2
Q

Neoplastic pluripotential development pattern of fibroblasts; retrocuspid papilla of Hirshfield (between free gingiva and mucogingival line)

A

Giant cell fibroma

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3
Q

Teenagers and young adults; bosselated or papillary surface; sessile or pedunculated base; gingiva>tongue>palate>buccal mucosa; Mandibular gingiva 2:1 over maxillary

A

Giant cell fibroma

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4
Q

Caused by irritation from ill-fitting denture; rolls of tissue associated with a denture flange; slowly growing, firm or compressible; lesion will not completely resolve by just removing denture

A

Epulis fissuratum

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5
Q

Reactive lesion; Only on gingiva; fixed mucosa, frequently ulcerated; firm, well-circumscribed; more common in adolescents and young adults; recurs in up to 20% of cases

A

Peripheral ossifying fibroma

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6
Q

Reactive; exuberant granulation tissue anywhere on body; most common on gingiva; often ulcerated; common during pregnancy and puberty

A

Pyogenic granuloma

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7
Q

Initially may have a rapid/alarming growth rate; very vascular: red or blue color, easily bleeds, may blanche upon pressure, compressible, spongy

A

Pyogenic granuloma

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8
Q

Reactive; Located only on gingiva most frequently anterior to the molars; fixed to mucosa

A

Peripheral giant cell granuloma

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9
Q

Vascular: red or blue/purple in color; easily bleeds; firm to palpation, may blanche upon pressure; often ulcerated; handful reported associated with hyperparathyroidism

A

Peripheral giant cell granuloma

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10
Q

Reactive proliferation of neural tissue after transection or damage of a nerve bundle; growth of axons through a tube of proliferating Schwann cells

A

Traumatic neuroma

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11
Q

Non-ulcerated nodules; most common in the mental foramen area, tongue, and lower lip; frequently a hx of trauma

A

Traumatic neuroma

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12
Q

Benign neoplasm of Schwann cells (myelin sheath around nerve axons); slow growing; firm and nonpainful; may be freely moveable

A

Schwannoma

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13
Q

Palisading nuclei; Verocay bodies (Antoni A-cellular; Antoni B-hypocellular); S-100 protein positivity

A

Schwannoma

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14
Q

Benign nerve sheath tumor in peripheral nervous system; 90% are stand-alone- the remainder are found in persons with NF1; von Recklinghausen

A

Neurofibroma

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15
Q

Fixed to the skin, surface mucosa and/or deep structures; firm or compressible, slowly growing and nonpainful; solitary or part of NF1

A

Neurofibroma

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16
Q

Six or more cafe-au-lait spots; two or more neurofibroma; axillary or inguinal freckling; two or more Lisch nodules

A

Neurofibromatosis

17
Q

Elongated cells with wavy nuclei (“jumping dolphins”); S-100 or silver stain

A

Neurofibroma

18
Q

Neural tissue origin can develop on any skin or mucosal surface, tongue-most common site; firm, slowly growing; fixed to surrounding structures; hyperplasia of overlying epithelium resulting in a rough surface

A

Granular cell tumor

19
Q

Large cells with granular, eosinophilic cytoplasm; pseudoepitheliomatous hyperplasia of overlying stratified squamous epithelium; can have demoplastic changes

A

Granular cell tumor

20
Q

Seen in newborns; Mesenchymal tissue- protruding mass from the alveolar ridge; female predilection; maxillary ridge is most common; feeding and/or respiratory problems

A

Congenital epulis of the newborn

21
Q

Histo- appear idential to granular cell tumor; no pseudo-epitheliomatous hyperplasia; s-100 positive; vimentin poisitive

A

Congenital epulis of the newborn

22
Q

Broad group of benign vascular tumors; most common soft tissue tumor of childhood; most common parotid tumor of children; adult tumors are smaller

A

Hemangioma and vascular malformation

23
Q

Subtypes: capillary (most common), juvenile (cellular), cavernous, vascular malformation; flat red-blue to red and exophytic; plump endothelial cells forming lumina; may regress spontaneously

A

Hemangioma and vascular malformation

24
Q

Benign developmental malformation of lymph vessels; neck is most common site; intraoral-tongue; pebbly surface-compressible mass; then walled lymph vessels around normal structures

A

Lymphangioma

25
Q

Syndrome association: Turner, Noonan, Trisomies; 3 types: capillary (small thin walled lymphatics), cavernous (larger channels with thickened lining), cystic hygroma (macroscopic spaces dissecting collagen and muscle)

A

Lymphangioma

26
Q

Benign neoplasm composed of mature adipose tissue; most lesions are solitary; most apparent in older age groups; some familial forms

A

Lipoma

27
Q

Slowly growing, spongy or compressible; may be freely-moveable; Superficial-most common in upper back, neck and shoulder; Deep- forehead and scalp

A

Lipoma

28
Q

Malignant tumors of epithelial origin

A

carcinomas

29
Q

Malignant tumors of mesenchymal origin

A

sarcomas

30
Q

Malignancy of striated muscle; most common soft tissue sarcoma of children and young adults; rapid growth; slight male predominance

A

Rhabdomyosarcoma

31
Q

4 subtypes: embryonal (head/neck, GU tract, retroperitoneum); botryoid (vagina, urinary bladder, nasal cavity); alveolar (extremities, head and neck); pleomorphic (extremities)

A

Rhabdomyosarcoma