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CYTOPHAGIC HISTIOCYTIC PANNICULITIS: REPORT OF TWO CASES

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 effusions, pancyto...

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Autors principals: Manoj, Jayasree, Kaliyadan, Feroze, Unni, Manoj, Dharmaratnam, A D
Format: Artigo
Idioma:Inglês
Publicat: Medknow Publications 2011
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3132910/
https://ncbi.nlm.nih.gov/pubmed/21772594
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5154.82487
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