red and pigmented soft tissue lesions Flashcards

1
Q

clinical presentation of oral melanotic macule

A

painless flat brown patches, usually evenly pigmented, less than 1cm usually single.

does not enlarge further once certain size is reached, does not become darker

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2
Q

common sites of oral melanotic macule

A

h. Sites
Lower lip, gingiva, buccal mucosa

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3
Q

tx of Oral melanotic macule

A

i. Treatment
Best excised, does not recure following excision

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4
Q

how does IO mucosa nevus occur

A

a. Nevus cells migrates into connective tissues. Clustered melanocytes with the ability to migrate to submucosa
Nevus cells are the projections from the stellate shape of the melanocytes

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5
Q

what are the clinical appearance of malignant melanoma

A

i. Asymmetry
ii. Border irregularity
iii. Color variegation
iv. Diameter more than 6mm
Elevation ( surface

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6
Q

what is the sites for malignant melanoma

A

palate, maxillary gingiva

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7
Q

where does amalgam tattoo appear

A

In the vicinity of AR restored teeth, crowned teeth, endo, healed extraction socket

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8
Q

what is the histo of amalgam tattoo

A

i. Fine brown granules staining collagen fibres
ii. Reticulin fibers around blood vessels nerve; lack of inflammation
May or may not have giant cells present

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9
Q

what drugs can cause pigmentation

A

chx, minocycline, zidovudine, ketoconazole, bulsuphan

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10
Q

what is hemangioma

A

a. Common benign neoplasm of infancy
b. True neoplasm of endothelial cells

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11
Q

sites of hemangioma

A

i. Lips> tongue> cheek> palate

60% h and n region

uncommon intra oral

involutes by 5-9 yo

proliferative phase at 1 yo

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12
Q

clinical observation of hemangioma

A

Dark reddish purplish smooth, flat or raised lesion of soft consistency
h. Single> multiple
i. Blanch on pressure
j. Asymptomatic non progressive
k. Ulcerates, bleeds, may compress vital structures if larger. Asymptomatic

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13
Q

treatment of hemangioma

A

i. Watchful waiting for involution
ii. Intervene if life threatening, disfigurement
iii. Medical using beta blockers, corticosteroids
iv. Surgical
Laser

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14
Q

what is pyogenic granuloma

A

a. Non neoplastic proliferation of endothelial cells and capillaries in response to local injury
For eg plaque accumulation, trauma, pregnancy

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15
Q

what are the demographics and sites of pyogenic granuloma

A

b. Occurs in females more than males, peak in the 2nd decade
c. Site
Gingiva (>80%)

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16
Q

clinical observation of pyogenic granuloma

A

d. Painless sessile or pedunculated exohytic, red nodule with smooth or lobulated surface, surface may be ulcerated
Bleed easily, spontaneously under light pressure

17
Q

histology of pyogenic granuloma

A

i. Numerous endothelial lined channels engorged with RBC, may be organised in lobular pattern
ii. Surface may be ulcerated with mixed inflammatory infiltrate: neutrophils, plasma cells, lymphosites
Mature lesions are more fibrous

18
Q

treatment of pyogenic granuloma

A

i. Excision, low rate of recurrence
ii. Curettage of underlying tissue recommended
iii. Excision with 2mm margins at its clinical periphery and to a depth to the periosteum or to the causative agent
Foreign body, calculus or defective restoration should be removed as part of the exicision

19
Q

what is kaposi sarcoma

A

a. Vascular neoplasm of endothelial origin

associated with hhv8

20
Q

what is the treatment of kaposi sarcoma

A

i. For localised small lesion: local excision, intralesional injection of chemotherapeutic agents
ii. For larger lesions: radiotherapy
iii. Extensive cutaneous lesions: chemotherapy, AZT, HAART

21
Q

what is the histology of kaposi sarcoma

A

Presents as intramucosal nodule with prominent vascular channel lined by atypical endothelial/spindle cells and areas of extravasated rbcs with haemosiderin

22
Q

what is lymphagioma

A

§ Histo:
□ Capillary or mostly cavernous endothelial lined spaces containing lymph
§ Malformed dilated lymphatic channels or cysts of varying sizes
§ Results in accumulation of excess lymphatic fluid in affected area
§ Uncommon, diagnosed at birth or within 2 years old
§ Treatment
Usually don’t do anything, observation

23
Q

what is AVM

A
  • Genetic anomalies of vasculature resulting in fistulous connections between arterial and venous vessels; leading to high flow
  • Present at birth, persistent, common
  • Present intraorally on tongue, FOM, buccal mucosa, palate, intraosseous
  • Clinical findings
    ○ Pulsatile mass, palpable thrill, audible bruit
  • Intra-oral signs and symptoms
    Tooth mobility, bluish discolouration of gingiva, diffused poorly demarcated radiolucency, life threatening bleed after exo
24
Q
A