Ch. 10 - Granulomatous and histiocytic diseases Flashcards
Recite some categories of granulomas.
Sarcoidal (little surrounding infiltrate)
Tuberculoid (caseous necrosis)
Palisading (necrobiosis, foreign material)
Suppurative (neutrophils)
Granuloma annulare
Palisaded or interstitial granulomas in the upper dermis, with mucin. No cholesterol clefts, rare plasma cells.
Actinic granuloma
Palisading granuloma with no mucin. Solar elastosis engulfed by giant cells and histiocytes. Central loss of elastic tissue.
Necrobiosis lipoidica
(cause?)
Horizontal palisading granuloma with no mucin. Cholesterol clefts and plasma cells.
(diabetes-associated)
Rheumatoid nodule
Large palisading granuloma surrounding eosinophilic fibrin. In deep dermis and subcutis. No mucin.
Lupus miliaris disseminatus faciei (acne agminata)
Pea-like palisaded granuloma with central caseous necrosis. Resembles miliary TB, but actually rosaceous.
Sarcoidosis
Epithelioid histiocytes forming discrete “naked” granuloma with minimal lymphocyte infiltrate and no necrosis. Can have schaumann bodies and asteroid bodies.
What diseases should be considered in the differential for “naked” granulomas?
Sarcoidosis
Cutaneous crohn’s disease
Cheilitis granulomatosa
Tuberculoid leprosy
Silica/zirconium/beryllium granuloma
Granulomatous rosacea
Necrotic xanthogranuloma
Granuloma with touton giant cells and x-shaped necrosis. Cholesterol clefts, neutrophilis debris, and lymphoplasmacytic follicles.
Xanthogranuloma
Sea of histiocytes in dermis with later wreath giant cells and touton giant cells. No necrosis.
Reticulohistiocytic granuloma (solitary reticulohistiocytoma)
Sea of histiocytes in dermis with punched out lacunae and two-toned cytoplasm. Dense glassy eosinophilic cytoplasm.
Rosai-Dorfman disease (sinus histiocytosis with massive lymphadenopathy)
(IHC?)
Fibrotic nodules with sheets of lymphocytes and histiocytes. Emperipolesis (chronic inflammatory cells within histiocytes).
S100+, CD1a-, CD68+
Langerhans cell histiocytosis (histiocytosis X)
(IHC?)
Polymorphous infiltrate with edema, hemorrhage, and reniform nuclei. Folliculotropism.
S100+, CD1a+, Langerin+
Recall 3 forms of langerhans cell histiocytosis.
Letterer-Siwe: Disseminated and involves multiple organs
Hand-Schuller-Christian: DI, exophthalmos, lytic bone lesions
Eosinophilic granuloma: Localized to one site.
What are xanthomas?
Accumulations of lipid in histiocytes. Can be due to disorders of lipoprotein metabolism or plasma cell dyscrasia.