Abstract
A 33 year old man developed fever, malaise, jaundice, pancytopenia, coagulation abnormalities, hepatomegaly, pleural effusions and a subcutaneous lump. Biopsies revealed a lobular panniculitis with the presence of cytophagic histiocytes; erythrophagocytosis was also demonstrated in the liver and bone marrow. Despite the use of chemotherapy (CHOP) his clinical condition deteriorated and he died 5 months after presentation. This illness is consistent with the recently described syndrome of histiocytic cytophagic panniculitis.
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CITATION STYLE
Hilton, D. A., O’Malley, B. P., & Durrant, S. T. S. (1990). Histiocytic cytophagic panniculitis. Postgraduate Medical Journal. BMJ Publishing Group. https://doi.org/10.1136/pgmj.66.781.958
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