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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Wolters Kluwer Medknow Publications,
2011-01-01T00:00:00Z.
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