Dermatopathology II Flashcards

1
Q

Dermatofibroma (5):

A
  • Benign fibrous histiocytoma
  • Slow growing
  • Flesh-colored to pigmented papule
  • Displays the “dimple sign”
  • Fibrous reaction to some past trauma
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2
Q

Dermatofibroma histological features (3):

A
  • Benign proliferations of fibroblasts with collagen
  • Whirling fibroblasts with collagen bundles
  • May be overlying hyperkeratosis and hyperpigmentation
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3
Q

Uticaria pigmentosa (2):

A
  • Type of mastocytosis
  • Usually multiple mastocytomas - round to oval, red-brown papules and plaques, pruritic and may blister, appear shortly after birth
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4
Q

Systemic mastocytosis (3):

A
  • Usually adults
  • Skin lesions similar to uticaria pigmentosa plus:
    • Multi-organ mast cell infiltration
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5
Q

Mastocytoma histologic features (4):

A
  • Metachromatic granules within dendritic mast cells
  • Monomorphous dermal infiltrate
  • No epidermotropism
  • Fried egg cells
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6
Q

Ichthyosis:

A

Disorders which impair epidermal maturation

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7
Q

Irritant contact dermatitis (3):

A
  • Substance has direct toxic effects on the skin
  • Not an immunologic condition
  • Rash begins shortly after exposure
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8
Q

Allergic contact dermatitis (3):

A
  • Cell-mediated, delayed-type hypersensitivity reaction (Type IV)
  • Sensitization of skin occurs 1-2 weeks after 1st exposure to allergen
  • Reexposure causes dermatitis in hours to days
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9
Q

Atopic dermatitis (2):

A
  • Chronic, waxing and waning, extremely pruritic condition beginning in the 1st year of life
  • Condition is worse in winter due to decreased humidity
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10
Q

Lichenification:

A

Epidermal thickening characterized by visible and palpable skin thickening with accentuated skin lines
- Chronic dermatitis leads to this

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11
Q

Nummular dermatitis (3):

A
  • Coin shaped
  • Itchy red plaques with vesicles and distinct borders
  • More likely in young adults
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12
Q

Asteatotic dermatitis (3):

A
  • Winter itch
  • Older people in winter
  • Dry, cracked skin that becomes itchy
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13
Q

Erythema multiforme (EM) (4):

A
  • Immune-mediated, hypersensitivity reaction resulting in epidermal cell injury
  • Epidermal cells are attacked by CD8+ cytotoxic T-cells; target Ag unknown
  • Erythematous macules and papules, vesicules and bullae on extremities that are strikingly symmetric
  • Target lesions are diagnostic
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14
Q

Stevens-Johnson Syndrome (4):

A
  • 10-30% Body surface involvement
  • More severe than EM
  • Involvement of mucous membranes including mouth and conjunctivae
  • Systemic manifestations may include fever, difficulty eating, renal failure and sepsis
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15
Q

Toxic Epidermal Necrolysis (TENs) (4):

A
  • > 30% body surface involvement
  • More severe than Stevens-Johnson syndrome
  • Dermatologic emergency
  • Detachment of large areas of epidermis
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16
Q

Pityriasis rosea (6):

A
  • Subacute spongiotic dermatitis
  • Most common in winter
  • Get initial herald patch that resembles ring worm
  • Progresses to generalized oval, slightly elevated, scaling papules that are smaller
  • Lesions pink with scaling near the border
  • Christmas tree pattern
17
Q

Venous insufficiency (2):

A
  • Venous incompetence causes increased hydrostatic pressure and capillary damage leading to extravasation of RBCs and serum
  • Starts as edema and hyperpigmentation and leads to pruritic erythema and stasis dermatitis
18
Q

Psoriasis (5):

A
  • Accelerated proliferation of skin cells resulting in scaling
  • Chronic condition with exacerbations and remissions
  • Well-demarcated, erythematous plaques and papules with silver scaling
  • Symmetrical
  • Auspitz’s sign
19
Q

Auspitz’s sign:

A

Pinpoint bleeding on removed of scale

20
Q

Psoriasis histologic features (4):

A
  • Downward elongation of rete ridges
  • Thinning of overlying stratum granulosum with parakeratosis above
  • Aggregates of neutrophils with surrounding spongiosis
  • Capillaries in dermal papillae are brought close to the surface
21
Q

Arthritis multilans:

A

Very destructive form of psoriatic arthritis with significant periarticular bone resorption.

22
Q

Seborrheic dermatitis (4):

A
  • Chronic inflammatory process affecting areas rich in sebaceous glands
  • Malassezia furfur
  • Yellow greasy scaly patches with surrounding erythema
  • Asymptomatic but may be itchy
23
Q

Lichen planus (6):

A
  • Idiopathic inflammatory disorder
  • Pruritic, purple, polygonal, planar, papules, plaques
  • Most common on wrists and ankles
  • Mucous membrane involvement is common
  • Wickhams striae
  • Koebner phenomenon
24
Q

Wickham’s striae:

A

Fine reticulated white lines

25
Q

Koebner phenomenon:

A

Trauma to skin and stress can cause exacerbations

26
Q

Systemic lupus erythematosus:

A

Multisystem autoimmune disease involving connective tissues and blood vessels

27
Q

Malar rash:

A

SLE:

- Butterfly rash, erythematous, confluent, macular eruption with clear borders that spares nasolabial folds