Derm Histo Flashcards

1
Q

abnormal, premature keratinization in cells below s. granulosum;

A

dyskeratosis

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2
Q

loss of intercellular connections b/w keratinocytes

A

acanthoLYSIS

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3
Q

epidermal intercellular edema

  • fluid b/w cells –> clear spaces b/w; clear separation
A

SPONGIOsis

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4
Q

diffuse epidermal hyperplasia

(thickening of epidermis –> seeing elongation of rete pegs)

A

acanTHOSIS

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5
Q

d/c of the skin w/ INCOMPLETE loss of epidermis

(layer of skin is missing)

A

erosion

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6
Q

d/c of skin w/ COMPLETE loss of epidermis & often part of dermis/subcutis

(a deeper lesion)

A

ulceration

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7
Q

thickening of stratum corneum by abnormal keratin

A

hyperkeratosis

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8
Q

retention of nuclei in stratum corneum;

indication fo something irritating the skin but can’t clear the nuclei in time

A

PARAkeratosis

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9
Q

(*won’t be asked bc it’s so subtle & nonspecific)

Which ACUTE dermatosis?

  • Sparse superficial perivascular infiltrate of mononuclear cells, neutrophils, and esoinophils
  • Dermal edema: widely spaced collagen bundles
    • Angioedema
  • Dilated superficial lymphatic channels
A

URTICARIA

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10
Q

Which acute dermatosis?

  • spongiosis of the epidermis –>
  • intraepidermal vesicles or blister formation
  • Superficial perivascular lymphocytic infiltrate, dermal edema, eosinophils
A

Acute eczematous dermatitis

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11
Q

Which acute dermatosis?

  • lymphocytes accumulate along dermoepidermal junction; where they are assoc w/ degenerating & necrotic keratinocytes
  • Superficial perivasc lymphocytic infiltrate w/ dermal edema
  • No chronic changes (i.e. epidermal atrophy, hyperplasia or hyperkeratosis)
A

ERYTHEMA MULTIFORME;

  • lymphocytes accumulate along dermoepidermal junction; where they are assoc w/ degenerating & necrotic keratinocytes
  • Superficial perivasc lymphocytic infiltrate w/ dermal edema
  • No chronic changes (i.e. epidermal atrophy, hyperplasia or hyperkeratosis)
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12
Q

which chronic dermatosis?

  • acanthosis (epidermal thickening) w/ downward elongations of rete ridges;
  • thinned or absent granular layer w/ extensive parakeratosis
  • Thin suprapapillary plates (epi layer overlying tips of dermal papillae)
  • *Munro microabscesses: aggregates of neutrophils w/in parakeratotic scale
A

PSORIASIS

(assoc w/ MUNRO MICROABSCESSES)

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13
Q

which chronic dermatosis?

  • interface dermatitis (dense lichenoid lymphocytic infiltrate along dermoepidermal jxn assoc. w/ degenerated & necrotic keratinocytes)
  • Saw toothing (angulated zig-zag contour of the dermoepidermal interface; border changes; “hinting”)
  • Colloid or Civate bodies (anucleate, necrotic keratinocytes in papillary dermis)
  • Chronic changes (epidermal hyperplasia or atrophy; hypergranulosis & hyperkeratosis)
A

LICHEN PLANUS

(histo: bandlike infiltrate of lymphocytes at dermal-epidermal jxn & saw-tooth rete ridges)

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14
Q

which chronic dermatosis?

  • acantholysis (common histo feature); blisters form at diff’t levels w/in skin (suprabasal is most common)
  • Superficial dermal inflammatory infiltrate of lymphocytes, histiocytes, eosinophils
A

Pemphigoid vulgaris

(contains antibodies against desmoglein 3 – direct immunofluorescence: lesional skin shows characteristic netlike pattern of intercellular IgG deposits

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15
Q

which chronic dermatosis?

  • subepidermal nonacantholytic blister; *eosinophils present in blister;
  • Superficial and deep perivasc infiltrate w/ lymphocytes, eosinophils, neutrophils
A

BULLOUS PEMPHIGOID

direct immunofluorescence → LINEAR deposition of immunoglobulin & complement at dermo-epidermal jxn (ribbon candy pattern)

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16
Q

which chronic dermatolosis?

  • early lesions w/ fibrin & neutrophils accumulating at tips of dermal papillae → microabscesses → w/ minute foci of dermo-epidermal separations (microblisters)
  • Microblisters coalesce → form true subepidermal blisters
A

DERMATITIS HERPETIFORMIS:

  • direct immunofluorescence: granular deposits of IgA at the tops of dermal papillae; antigliadin antibodies to dietary gluten
  • Cross react to components of anchoring fibrils in skin
17
Q

which chronic dermatosis?

  • lesions show widening of CT septa due to edema, fibrin, neutrophils, lymphocytes, histiocytes, giant cells, occasional eosinophils, & septal fibrosis; typically NO VASCULITIS
A

ERYTHEMA NODOSUM

18
Q

which viral infection?

  • epidermal hyperplasia;
  • koliocytosis (viral cytopathic effect);
  • cytoplasmic vacuolization and pale halos surrounding infected nuclei;
  • coarse keratohyaline granules
A

VERRUCAE (virus);

  • papillar projections, dense granular cell layer*
  • coarse keratohyaline granules*
19
Q

which derm path?

most superficial nevus cells are immature, larger, and melanin-producing; deeper cells are mature, smaller, fusiform, and do not produce pigment

A

MELANOCYTIC NEVI

  • Junctional nevi: (flat) nests of melanocytes along dermo-epidermal jxn
  • Compound n.: (*elevated) nests of melanocytes along dermo-epi jxn & dermis
  • Dermal n.: (*elevated) nests of melanocytes in dermis only
20
Q

which derm path?

  • nevus nests are large and fuse w/ each other
  • Melanocytic atypia w/ irregular hyperchromatic nuclei
  • Lymphocytic infiltrate in the upper dermis
  • Linear dermal fibrosis around the rete ridges
A

DYSPLASTIC NEVI

21
Q

which type of malignant melanoma growth?

melanoma cells tend to grow HORIZONTALLY along epidermis & superficial dermis; no metastatic potential

A

Radial growth phase

22
Q

which type of malignant melanoma growth?

melanoma cells grow vertically in deeper dermis w/ no maturation and acquire metastatic potential

A

Vertical growth phase

23
Q

type of nevi?

large cells w/ large irregular nuclei;

clumped chromatin & prominent red nucleoli growing as individual cells or poorly defined nests at all levels of epidermis (radial growth) and dermis (vertical growth)

A

MALIGNANT MELANOMA

24
Q

which derm path?

  • Exophytic, well-demarcated
    • Composed of sheets of basal epidermal cells w/ melanin pigmentation and hyperkeratosis in the form of keratin filled cysts (horn cysts)
    • Can occur in large numbers as part of paraneoplastic syndrome (Leser-Trelat sign); most commonly assoc w/ adenocarcinoma of stomach
  • Exophytic: tending to grow outward beyond the surface epithelium from which it originated
A

Seborrheic keratosis

25
Q

which derm path?

(microscopically) fibrovascular cores covered by benign squamous epithelium

A

Fibroepithelial polyp

26
Q

which derm path?

  • Invaginations and cystic expansion of epidermis, filled w/ keratin and lipid debris
  • Creates intense inflammation if ruptured
A

Epithelial cysts (Wen)

27
Q

which derm path?

  • Parakeratosis; cytologic atypia of lower most epidermal cell layer, assoc. w/ hypertrophic and atrophic epidermis
  • Elastosis (blue-gray elastic fibers) in the upper dermis, resulting from sun-damaged fibroblasts
A

ACTINIC KERATOSIS

28
Q

which derm path?

  • atypical enlarged hyperchromatic cells at all levels of epidermis
  • Confined w/in epidermis; in situ - or invading through basement membrane into dermis (invasive)
A

Squamous cell carcinoma

29
Q

which derm path?

  • tumor cells resemble basal keratinocytes;
  • Tumor islands show palisading peripherally (long axes of the cells is in parallel alignment)
A

BASAL CELL CARCINOMA

30
Q

which derm path?

  • benign dermal neoplasm of fibroblasts and histiocytes
  • Benign, spindle-shaped fibroblasts arranged in well-defined mass in mid-dermis –> mixed w/ variable amounts of foamy histiocytes
  • Overlying epidermal hyperplasia
A

Benign fibrous histiocytoma (Dermatofibroma)

31
Q

which derm path?

  • Morph: cellular neoplasm, fibroblasts arranged in storifom pattern;
  • Thin overlying epidermis
  • Extension into subcutaneous tissue
A

Dermatofibrosarcoma protuberans