Moriki T, Wada M, Takahashi T, Ueda S, Miyazaki E
Departments of Clinical Laboratory and Pathology, Kochi Medical School and Kochi Medical School Hospital, Nankoku, Kochi, Japan.
Acta Cytol. 2000 Nov-Dec;44(6):1040-4. doi: 10.1159/000328594.
Cytophagic histiocytic panniculitis (CHP) presents with subcutaneous panniculitis associated with hemophagocytic syndrome. Many cases of CHP are now being classified as a natural disease progression of subcutaneous panniculitic T-cell lymphoma (SPTL). There have been no cytologic reports dealing with pleural aspirates in cases of CHP or SPTL.
A pleural aspirate obtained from a 19-year-old female revealed lymphoma cells and hemophagocytic histiocytes. A skin biopsy specimen showed the presence of CD8-positive lymphoma cells in fat lobules associated with cytologically benign histiocytes with erythrophagocytosis and lymphophagocytosis.
Hemophagocytic histiocytes were seen in the pleural effusion from a patient with SPTL.