The Skin Flashcards

1
Q

Disease of depigmentation secondary to destruction of melanocytes.

A

Vitilligo

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2
Q

Disease of depigmentation secondary to decreased or absent synthesis of melanin.

A

Albinism

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3
Q

These are nevi, usually <6 mm, benign-looking, clinically and histologically, and are removed for cosmetic reasons; these lesions have RAS mutations but most never progress because of intact p16 (tumor-suppressor) activity.

A

Melanocytic nevus

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4
Q

These are large nevi (>5 mm) and may occur as hundreds of lesions on the body surface; they are flat macules to slightly raised plaques, with a “pebbly” surface; considered as a marker of melanoma risk.

A

Dysplastic nevi

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5
Q

The most deadly of all skin cancers; results from excessive sun exposure; malignant cells have large nuclei with irregular contours having chromatin characteristically clumped at the periphery of the nuclear membrane and prominent eosinophilic nucleoli often described as “cherry red”; has both radial and vertical growth phases.

A

Melanoma

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6
Q

Immunohistochemical staining for melanoma.

A

S-100, and HMB-45 (more specific)

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7
Q

Clinically mimics melanoma; round, exophytic, coin-like plaques varying in diameter, with a velvety/granular surface; tan to dark brown in color; it has a stuck-on appearance often seen in older individuals; the lesions consist of an orderly proliferation of uniform, monotonous sheets of small cells (basaloid in appearance) with a tendency to form keratin microcysts (horn cysts).

A

Seborrheic keratosis

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8
Q

This lesion is usually the result of chronic exposure to sunlight; dermis contains thickened, blue-gray elastic fibers or “solar elastosis” which is the result of chronic sun damage; grossly, lesions are less than 1cm, tan-brown or red in color, with sandpaper-like surface; microscopically, there is Atypical dyskeratotic cells in basal epidermis with intercellular bridges, solar elastosis, hyperparakeratosis and dermal chronic inflammation.

A

Actinic keratosis

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9
Q

A common tumor arising on sun-exposed sites in older people, with higher incidence in women; may arise from prior actinic keratoses, then when advanced becomes nodular and may ulcerate; characterized by anaplastic (seen on all levels of the epidermis), rounded cells with foci of necrosis and only abortive, single-cell keratinization (dyskeratosis).

A

Squamous cell carcinoma

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10
Q

This is the most common human cancer, which is a slow-growing tumor that rarely metastasizes; tends to occur at sites subject to chronic sun exposure and in lightly pigmented people; These tumors present as pearly, smooth-surfaced papules, often containing prominent, dilated subepidermal blood vessels (telangiectasia); the cells have scant cytoplasm, small hyperchromatic nuclei, and a peripheral palisade with clefting from the stroma.

A

Basal cell carcinoma

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11
Q

Condition caused by local mast cell degranulation; histologically, there is usually a sparse superficial perivenular infiltrate of mononuclear cells with superficial dermal edema.

A

Urticaria

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12
Q

This term is the accumulation of edema fluid within the epidermis; characterizes all forms of eczamatous dermatitis.

A

Spongiosis

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13
Q

An uncommon, usually self-limited disorder that seems to be a hypersensitivity response to certain infections and drugs; patients present with an array of “multiform” lesions, including macules, papules, vesicles, and bullae, as well as the characteristic targetoid lesion consisting of a red macule or papule with a pale vesicular or eroded center; part of a spectrum with SJS-TEN.

A

Erytherma multiforme

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14
Q

A skin disorder whose main pathology is increased epithelial cell turnover; there is acanthosis and loss of the stratum granulosum with extensive overlying parakeratotic scale; there is also a regular downward elongation of rete ridges (test tubes in a rack appearance); associated with multiple punctate hemorrhages upon removal of scales from the lesions (Auspitz sign) due to presence of dilated tortuous vessels.

A

Psoriasis

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15
Q

Small aggregates of neutrophils within the parakeratotic stratum corneum (Munro microabscesses); and spongiotic superficial epidermis (Pustules of Kogoj) are findings associated with:

A

Psoriasis

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16
Q

“Pruritic, purple, polygonal, planar papules, and plaques” describes this disorder of the skin and mucosa. Also noted grossly are Wickham striae, which are white lacelike markings over the papules; pattern of inflammation of this disorder is characterized by angulated, zigzag contour (“sawtoothing”) of the dermoepidermal junction.

A

Lichen planus

17
Q

A rare autoimmune blistering disorder resulting from loss of integrity of normal intercellular attachments within the epidermis and mucosal epithelium; caused by a Type II hypersensitivity reaction (mainly IgG) against desmoglein; histologically characterized by acantholysis immediately above the basal layer.

A

Pemphigus vulgaris

18
Q

Also an autoimmune (IgG-mediated against bullous pemphigoid antigens) blistering disease against the epidermal basement membrane components (hemidesmosomes); however, it is characterized by subepidermal nonacantholytic blisters.

A

Bullous pemphigoid

19
Q

Associated with celiac disease; clinically characterized by pruritic urticarial; histologically characterized by subepidermal blisters that develop from coalescence of vacuolized microabscesses at the dermal papilla tips.

A

Dermatitis herpetiformis

20
Q

A skin infection caused by either S. aureus (characterized by formation of bullae) or S. pyogenes (characterized by appearance of honey-colored crusts); histologically characterized by subcorneal neutrophilic infiltration.

A

Impetigo

21
Q

A benign lesion cause by low-risk strains of HPV (2, 4 and 7); characterized by koilocytic atypia (cytoplasmic vacuolization).

A

Verrucae