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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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Bibliografski detalji
Glavni autori: Manoj, Jayasree, Kaliyadan, Feroze, Unni, Manoj, Dharmaratnam, A D
Format: Artigo
Jezik:Inglês
Izdano: Medknow Publications 2011
Teme:
Online pristup: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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