Volume 18, Issue 6 pp. 713-715

A case of subcutaneous panniculitis-like T-cell lymphoma with haemophagocytosis developing secondary to chemotherapy

B Eser

Corresponding Author

B Eser

Departments of Hematology–Oncology

*Corresponding author, Erciyes Üniversitesi Tip Fakültesi, M.K. Dedeman Hastanesi, Hematoloji Bilim Dali, Kayseri, Turkey, tel. +90 352 4374937/27031; fax +90 352 4379348; E-mail: [email protected]Search for more papers by this author
F Altuntas

F Altuntas

Departments of Hematology–Oncology

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O Er

O Er

Departments of Hematology–Oncology

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O KontasA Ferahbas

A Ferahbas

Dermatology, Erciyes University School of Medicine, Kayseri, Turkey.

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M Cetin

M Cetin

Departments of Hematology–Oncology

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A Unal

A Unal

Departments of Hematology–Oncology

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First published: 21 September 2004
Citations: 6

ABSTRACT

A 45-year-old woman presented with fever, generalized skin lesions and multiple lymphadenopathies. In her past history she had had six courses of cyclophosphamide and cisplatin combination chemotherapy 7 years ago because of an ovarian carcinoma. We found pancytopenia in the peripheral blood examination. Skin biopsy showed diffuse subcutaneous infiltration reminiscent of panniculitis but composed of malignant lymphoid cells that were of T lineage. Bone marrow biopsy showed normocellular myeloid tissue with abundant haemophagocytic macrophages. Subcutaneous panniculitis-like T-cell lymphoma with haemophagocytic syndrome was diagnosed. This is the first case reported of subcutaneous panniculitis-like lymphoma occurring secondary to chemotherapy.

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