Ch. 10 - Granulomatous and histiocytic diseases Flashcards

1
Q

Recite some categories of granulomas.

A

Sarcoidal (little surrounding infiltrate)

Tuberculoid (caseous necrosis)

Palisading (necrobiosis, foreign material)

Suppurative (neutrophils)

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2
Q

Granuloma annulare

A

Palisaded or interstitial granulomas in the upper dermis, with mucin. No cholesterol clefts, rare plasma cells.

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3
Q

Actinic granuloma

A

Palisading granuloma with no mucin. Solar elastosis engulfed by giant cells and histiocytes. Central loss of elastic tissue.

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4
Q

Necrobiosis lipoidica

(cause?)

A

Horizontal palisading granuloma with no mucin. Cholesterol clefts and plasma cells.

(diabetes-associated)

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5
Q

Rheumatoid nodule

A

Large palisading granuloma surrounding eosinophilic fibrin. In deep dermis and subcutis. No mucin.

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6
Q

Lupus miliaris disseminatus faciei (acne agminata)

A

Pea-like palisaded granuloma with central caseous necrosis. Resembles miliary TB, but actually rosaceous.

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7
Q

Sarcoidosis

A

Epithelioid histiocytes forming discrete “naked” granuloma with minimal lymphocyte infiltrate and no necrosis. Can have schaumann bodies and asteroid bodies.

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8
Q

What diseases should be considered in the differential for “naked” granulomas?

A

Sarcoidosis

Cutaneous crohn’s disease

Cheilitis granulomatosa

Tuberculoid leprosy

Silica/zirconium/beryllium granuloma

Granulomatous rosacea

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9
Q

Necrotic xanthogranuloma

A

Granuloma with touton giant cells and x-shaped necrosis. Cholesterol clefts, neutrophilis debris, and lymphoplasmacytic follicles.

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10
Q

Xanthogranuloma

A

Sea of histiocytes in dermis with later wreath giant cells and touton giant cells. No necrosis.

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11
Q

Reticulohistiocytic granuloma (solitary reticulohistiocytoma)

A

Sea of histiocytes in dermis with punched out lacunae and two-toned cytoplasm. Dense glassy eosinophilic cytoplasm.

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12
Q

Rosai-Dorfman disease (sinus histiocytosis with massive lymphadenopathy)

(IHC?)

A

Fibrotic nodules with sheets of lymphocytes and histiocytes. Emperipolesis (chronic inflammatory cells within histiocytes).

S100+, CD1a-, CD68+

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13
Q

Langerhans cell histiocytosis (histiocytosis X)

(IHC?)

A

Polymorphous infiltrate with edema, hemorrhage, and reniform nuclei. Folliculotropism.

S100+, CD1a+, Langerin+

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14
Q

Recall 3 forms of langerhans cell histiocytosis.

A

Letterer-Siwe: Disseminated and involves multiple organs

Hand-Schuller-Christian: DI, exophthalmos, lytic bone lesions

Eosinophilic granuloma: Localized to one site.

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15
Q

What are xanthomas?

A

Accumulations of lipid in histiocytes. Can be due to disorders of lipoprotein metabolism or plasma cell dyscrasia.

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16
Q

Xanthelasma

A

Band of foam cells in superficial or mid dermis. Eyelid location. Most common and unremarkable.

17
Q

Tuberous xanthoma

(cause?)

A

Fibrotic nodule with variable foam cells. Cholesterol clefts.

Indicates dyslipoproteinemias.

18
Q

Eruptive xanthoma

A

Foam cells and extracellular lipid, with sattered inflammatory infiltrate.

(very rapid lipid deposition resulting from increase in serum chylomicrons)

19
Q

Verruciform xanthoma

(cause?)

A

Papillomatosis with foam cells in the dermal papillae.

(may be due to degeneration of cells in the overlying epidermis)

20
Q
A

Interstitial granuloma annulare

21
Q
A

Palisading granuloma annulare

22
Q
A

Actinic granuloma

23
Q
A

Necrobiosis lipoidica

24
Q
A

Rheumatoid nodule

25
Q
A

Lupus miliaris disseminatus faciei (acne agnimata)

26
Q
A

Sarcoidosis

27
Q
A

Necrobiotic xanthogranuloma

28
Q
A

Xanthogranuloma

29
Q
A

Reticulohistiocytic xanthogranuloma

30
Q
A

Rosai-Dorfman disease

31
Q
A

Langerhans cell histiocytosis (histiocytosis X)

32
Q
A

Xanthelasma

33
Q
A

Tuberous xanthoma

34
Q
A

Eruptive xanthoma

35
Q
A

Eruptive xanthoma

36
Q
A

Verruciform xanthoma