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Reference

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A reference for what the literature reports. Not medical advice.

Disease

cytophagic histiocytic panniculitis

MONDO:0019789Mondo

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Findings

No curated finding names cytophagic histiocytic panniculitis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

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.

Definition from the Mondo Disease Ontology (MONDO:0019789), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: panniculitis
subcutaneous tissue disorder

Other names

2 names

Resolves to: cytophagic histiocytic panniculitis

Also called: CHPWinkelmann cytophagic panniculitis