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首页> 外文期刊>Leukemia and lymphoma >Successful treatment of refractory subcutaneous panniculitis-like T-cell lymphoma with allogeneic peripheral blood stem cell transplantation from HLA-mismatched sibling donor
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Successful treatment of refractory subcutaneous panniculitis-like T-cell lymphoma with allogeneic peripheral blood stem cell transplantation from HLA-mismatched sibling donor

机译:HLA不匹配同胞供者同种异体外周血干细胞移植成功治疗难治性皮下脂膜炎样T细胞淋巴瘤

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Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is an uncommon type of peripheral T-cell lymphoma (PTCL) usually presenting with erythe-matous, subcutaneous nodules and fever. It is considered as a cytotoxic T-cell neoplasm with cyo-toxic granules and can be cytochemically identified using granzyme B, perform or TIA-1. Some cases of SPTCL might be indolent for months or years, but SPTL frequently has an aggressive course, and is often complicated by fatal hemophagocytic syndrome (HPS).Among the cases of SPTCL, resistance to anthracyclin-based therapy generally means a poor prognosis. The use of high-dose therapy (HDT) with autologous stem cell transplantation (SCT) in patients with SPTCL who are refractory to anthra-cyclins has yielded good results. However, a cure can only be expected if the disease is at least sensitive to HDT. Allogeneic SCT, however, might yield a cure even in chemo-refractory lymphoma patients via a graft-vs.-lymphoma (GVL) effect. We report a case of successful use of an allogeneic peripheral blood stem cell transplantation (allo-PBSCT) from an HLA-mismatched sibling donor in a patient with SPTCL who was refractory to conventional chemotherapy.
机译:皮下脂膜炎样T细胞淋巴瘤(SPTCL)是一种罕见的周围性T细胞淋巴瘤(PTCL),通常表现为红斑,皮下结节和发烧。它被认为是具有Cyo毒性颗粒的细胞毒性T细胞肿瘤,可以使用颗粒酶B,perform或TIA-1进行细胞化学鉴定。某些SPTCL病例可能几个月或几年无痛发作,但SPTL经常具有侵袭性病程,并常伴有致命的噬血细胞综合征(HPS)。高剂量疗法(HDT)和自体干细胞移植(SCT)在对蒽环素难治的SPTCL患者中的使用已产生了良好的效果。但是,仅当疾病至少对HDT敏感时才能治愈。然而,即使在化学难治性淋巴瘤患者中,通过移植物抗淋巴瘤(GVL)效应,同种异体SCT仍可能治愈。我们报告了一个病例,该病例成功地从HLA不匹配的同胞供体中接受了异体外周血干细胞移植(allo-PBSCT),该患者患有常规化疗难以耐受的SPTCL患者。

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