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

0 clinical trials for this condition and its sub-types, 0 tagged with Cytophagic histiocytic panniculitis itself.

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↑ Subcutaneous tissue disorder (64) ↑ Panniculitis (6)

Including sub-types (0) Tagged with Cytophagic histiocytic panniculitis (0)

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