{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,2,5]],"date-time":"2024-02-05T11:43:35Z","timestamp":1707133415369},"reference-count":17,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2004,9,21]],"date-time":"2004-09-21T00:00:00Z","timestamp":1095724800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Acad Dermatol Venereol"],"published-print":{"date-parts":[[2004,11]]},"abstract":"<jats:title>ABSTRACT<\/jats:title><jats:p>A 45\u2010year\u2010old 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\u00a0years 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\u00a0lineage. Bone marrow biopsy showed normocellular myeloid tissue with abundant haemophagocytic macrophages. Subcutaneous panniculitis\u2010like T\u2010cell lymphoma with haemophagocytic syndrome was diagnosed. This is the first case reported of subcutaneous panniculitis\u2010like lymphoma occurring secondary to chemotherapy.<\/jats:p>","DOI":"10.1111\/j.1468-3083.2004.01043.x","type":"journal-article","created":{"date-parts":[[2004,10,11]],"date-time":"2004-10-11T15:40:55Z","timestamp":1097509255000},"page":"713-715","source":"Crossref","is-referenced-by-count":6,"title":["A case of subcutaneous panniculitis\u2010like T\u2010cell lymphoma with haemophagocytosis developing secondary to chemotherapy"],"prefix":"10.1111","volume":"18","author":[{"given":"B","family":"Eser","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F","family":"Altuntas","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"O","family":"Er","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"O","family":"Kontas","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A","family":"Ferahbas","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"Cetin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A","family":"Unal","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2004,9,21]]},"reference":[{"key":"e_1_2_4_2_2","first-page":"2447","volume-title":"Wintrobe's Clinical Hematology","author":"Greer JP","year":"1999"},{"key":"e_1_2_4_3_2","doi-asserted-by":"publisher","DOI":"10.1001\/archderm.136.7.889"},{"key":"e_1_2_4_4_2","first-page":"297","article-title":"Subcutaneous T\u2010cell lymphoma: a case report and additional observations","volume":"58","author":"Sajben FP","year":"1996","journal-title":"Cutis"},{"key":"e_1_2_4_5_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0190-9622(96)90077-8"},{"key":"e_1_2_4_6_2","first-page":"519","article-title":"Subcutaneous panniculitic T\u2010cell lymphoma with chromosomal abnormalities and large granular lymphocytes morphology","volume":"41","author":"Mizutani Y","year":"2000","journal-title":"Rinsho Ketsueki"},{"key":"e_1_2_4_7_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0190-9622(98)70044-1"},{"key":"e_1_2_4_8_2","first-page":"393","article-title":"Non\u2010Hodgkin's lymphoma secondary to Hodgkin's disease treated with chemo\u2010 and radiotherapy. 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