CYTOPHAGIC HISTIOCYTIC PANNICULITIS ASSOCIATED WITH HBE HEMOGLOBINOPATHY IN A PATIENT WITH HEMOPHAGOCYTIC SYNDROME
Introduction: Cytophagic histiocytic panniculitis (CHP) is a rare panniculitis which may occur alone or as a part of systemic manifestation of Hemophagocytic syndrome (HPS). It is described as a chronic histiocytic disorder of the subcutaneous adipose tissue with lymphocytic and histiocytic infiltra...
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