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Intensive Induction Chemotherapy Followed by Early High-Dose Therapyand Hematopoietic Stem Cell Transplantation Results in Improved Outcome forPatients with Hepatosplenic T-Cell Lymphoma: A Single InstitutionExperience

机译:密集的诱导化疗然后是早期高剂量治疗造血干细胞移植导致改善的结果患有肝瓣T细胞淋巴瘤的患者:单一机构经验

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摘要

Hepatosplenic T-cell lymphoma is a rare form of non-Hodgkin lymphoma, which carries a poor prognosis. We report our single-institution experience in the management of hepatosplenic T-cell lymphoma (HSTCL)- in 14 patients (pts) among whom 7 who remain alive (50%) and in remission at a median follow-up of 66 months. More frequent long-term survival was seen in those treated with a non-CHOP (cyclophosphamide/doxorubicin/vincristine/prednisone) induction and consolidative stem cell transplant (SCT).IntroductionHepatosplenic T-cell lymphoma is a rare form of extranodal non-Hodgkin lymphoma, first recognized as a distinct entity in the Revised European-American Lymphoma classification. Typical presentation includes lymphomatous infiltration of spleen and liver, and peripheral lymphadenopathy is rarely seen. The prognosis is almost uniformly poor, and there are no prospective studies of treatment of HSTCL.
机译:肝脾性T细胞淋巴瘤是一种罕见的非霍奇金淋巴瘤,预后较差。我们报告了单机构治疗肝脾T细胞淋巴瘤(HSTCL)的经验,其中14例患者(pt),其中7例仍然活着(50%),中位随访66个月后缓解。非CHOP(环磷酰胺/阿霉素/长春新碱/泼尼松)诱导和巩固干细胞移植(SCT)治疗的患者长期存活率更高。肝脾T细胞淋巴瘤是结节型非霍奇金淋巴瘤的一种罕见形式。 ,最初在经修订的欧美淋巴瘤分类中被认为是独特的实体。典型的表现包括脾脏和肝脏的淋巴瘤浸润,很少见到周围淋巴结肿大。预后几乎一致差,并且尚无前瞻性研究治疗HSTCL。

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