- histiocytic cytophagic panniculitis
- cytophagic histiocytic p.
Medical dictionary. 2011.
Medical dictionary. 2011.
Cytophagic histiocytic panniculitis — (CHP) was first described in 1980 by Winkelmann as a chronic histiocytic disease of the subcutaneous adipose tissue, which is characterized clinically by tender erythematous nodules, recurrent high fever, malaise, jaundice, organomegaly, serosal… … Wikipedia
Panniculitis — Classification and external resources ICD 10 M79.3 ICD 9 729.3 … Wikipedia
panniculitis — Inflammation of subcutaneous adipose tissue. [panniculus + G. itis, inflammation] α1 antitrypsin deficiency p. multiple painful subcutaneous nodules occurring in patients with severe antitrypsin deficiency … Medical dictionary
cytophagic histiocytic panniculitis — a severe variant of relapsing febrile nodular nonsuppurative panniculitis characterized by lobules infiltrated by histiocytes that have phagocytized erythrocytes, leukocytes, and platelets; it is sometimes accompanied by systemic conditions that… … Medical dictionary
List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… … Wikipedia
Lipodermatosclerosis — Classification and external resources DiseasesDB 30155 Lipodermatosclerosis (also known as Chronic panniculitis with lipomembranous changes, [1] Hypodermitis sclerodermiformis, Sclerosing panniculitis, a … Wikipedia
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