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Enteropathy-associated T-cell lymphoma: a review on clinical presentation, diagnosis, therapeutic strategies and perspectives.

机译:肠病相关的T细胞淋巴瘤:临床表现,诊断,治疗策略和观点的综述。

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INTRODUCTION: Enteropathy-associated T-cell lymphoma (EATL) is a rare complication of celiac disease (<1% of lymphomas) and has a poor prognosis. METHODS: International literature review with PubMed search (up to January 2009) of pathophysiological, clinical and therapeutic data. RESULTS: EATL is found in patients with a mean age of 59 years, often with a complication that signals its diagnosis. Refractory celiac disease (RCD), equivalent to low-grade intraepithelial T-cell lymphoma, could be an intermediary between celiac disease and high-grade invasive T-cell lymphoma. The median survival is 7 months, with no significant difference between stages; the cumulative 5-year survival is less than 20%. The poor prognosis is determined by disease that has often spread before it is diagnosed (50%), multifocal involvement of the small bowel (50%), poor general health status and undernutrition, and recurrence of complications (infections, perforations, gastrointestinal haemorrhages, occlusions), thus delaying the chemotherapy and contributing to frequent chemotherapy resistance. There is currently no effective and consensual treatment: preventive surgery for complications is controversial, and the results of chemotherapy are disappointing. The classic CHOP protocol (combination of doxorubicin-cyclophosphamide-vincristine-prednisone) does not have satisfactory results and survival remains poor, especially in patients with underlying RCD. High-dose chemotherapy with autotransplantion seems to only improve the prognosis in localised forms. Allogeneic bone marrow transplantation was not evaluated. In all, 1/3 of patients, being unfit for treatment, die before 3 months and half of treated patients stop chemotherapy prematurely due to inefficacy, intolerance and/or complications. CONCLUSION: Improvement of the prognosis requires collaboration in order to compose a national cohort, to evaluate new diagnostic and therapeutic strategies and to define prognostic factors.
机译:简介:与肠病相关的T细胞淋巴瘤(EATL)是一种罕见的乳糜泻并发症(<1%淋巴瘤),预后较差。方法:通过PubMed搜索(截至2009年1月)的病理生理,临床和治疗数据进行国际文献综述。结果:EATL发现于平均年龄为59岁的患者中,通常伴有并发症,提示其诊断。难治性腹腔疾病(RCD)等同于低度上皮内T细胞淋巴瘤,可能是腹腔疾病和高级别浸润性T细胞淋巴瘤之间的中介。中位生存期为7个月,各阶段之间无显着差异。累计5年生存率不到20%。预后不良取决于以下疾病:在诊断之前通常已扩散的疾病(50%),小肠多灶性受累(50%),总体健康状况和营养不良,并发症(感染,穿孔,胃肠道出血,闭塞),从而延迟了化疗并导致了频繁的化疗耐药性。目前尚无有效且协商一致的治疗方法:针对并发症的预防性手术尚有争议,化学疗法的效果令人失望。经典的CHOP方案(阿霉素-环磷酰胺-长春新碱-泼尼松的组合)未获得令人满意的结果,生存率仍然很差,尤其是对于有基础RCD的患者。自体移植的大剂量化疗似乎只能改善局部形式的预后。未评估同种异体骨髓移植。总共有1/3的不适合治疗的患者在3个月前死亡,一半的治疗患者由于无效,不耐受和/或并发症而过早停止化疗。结论:改善预后需要合作以组成一个全国性的队列,评估新的诊断和治疗策略并确定预后因素。

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