医学
长春新碱
噬血细胞性淋巴组织细胞增多症
依托泊苷
淋巴瘤
环磷酰胺
免疫学
养生
造血干细胞移植
造血干细胞
造血
干细胞
疾病
内科学
化疗
肿瘤科
生物
遗传学
作者
Nicholas Manini,Kimberly Davidow,Katrina Conard,Jonathan Powell
标识
DOI:10.1097/mph.0000000000002800
摘要
Systemic Epstein-Barr virus-positive T-cell lymphoma of childhood (S-EBV-TCL) is a rare disease for which there is no standard of care. S-EBV-TCL is often associated with hemophagocytic lymphohistiocytosis and is generally thought of on the spectrum of EBV-related disease. For the few reported cases of cure in the literature, hematopoietic stem cell transplant has been required because it is the only treatment that has induced complete remission in patients suffering from EBV-associated T-cell or natural killer cell lymphoproliferative diseases, except hemophagocytic lymphohistiocytosis. Here, we present the case of one patient who was successfully cured with a modified regimen of dose-adjusted EPOCH (etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin), followed by hematopoietic stem cell transplant using a reduced-intensity conditioning regimen.
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