Cytophagic histiocytic panniculitis

MONDO:0019789

Cytophagic histiocytic panniculitis (CHP) is a very rare form of panniculitis manifesting as recurrent multiple subcutaneous nodules (which may progressively become ecchymotic and ulcerated), and histologically characterized by lobular panniculitis with lymphocytic and histiocytic infiltration in the subcutaneous adipose tissue.

Also known as: CHP, Winkelmann cytophagic panniculitis

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Broader categories

Disease (680) Inflammatory disease (332) Connective tissue disorder (68) Human disease (14) Panniculitis (3) Disease by body system or component (0) Disease by developmental or physiological process (0) Integumentary system disorder (0) Subcutaneous tissue disorder (0)

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