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Long-term remission of subcutaneous panniculitis-like T-cell lymphoma with central nervous system involvement: A case report

机译:长期皮下脂膜炎样T细胞淋巴瘤伴中枢神经系统缓解:1例报告

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摘要

Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is an indolent cutaneous T-cell lymphoma with a favourable prognosis. The reported incidence of central nervous system (CNS) involvement in SPTCL is extremely low. SPTCL with CNS involvement is a fatal disease with no optimal treatment. The present study presents the case of a 27-year-old man who initially presented with erythematous nodules on the left buttock and left inguinal lymph node enlargement. A skin biopsy resulted in a diagnosis of SPTCL. Subsequent to diagnosis, the patient developed CNS involvement and underwent treatment of fotemustine, teniposide and dexamethasone, and complete remission was achieved for 78 months. To the best of our knowledge, this is the first case report of secondary CNS SPTCL with long-term remission. Accumulating evidence shows that this CNS-directed regimen can be effective in SPTCL with CNS involvement and in other CNS lymphomas.
机译:皮下脂膜炎样T细胞淋巴瘤(SPTCL)是一种惰性的皮肤T细胞淋巴瘤,预后良好。据报道,中枢神经系统(CNS)参与SPTCL的发生率极低。中枢神经系统受累的SPTCL是致命疾病,没有最佳治疗方法。本研究介绍了一个27岁男性的案例,该男性最初在左臀部出现红斑性结节,左腹股沟淋巴结肿大。皮肤活检诊断为SPTCL。诊断后,该患者发展为中枢神经系统受累,并接受了福莫汀,替尼泊苷和地塞米松的治疗,并在78个月内完全缓解。据我们所知,这是继发中枢神经系统SPTCL并具有长期缓解的首例病例报告。越来越多的证据表明,这种中枢神经系统定向治疗方案可有效治疗参与中枢神经系统感染的SPTCL和其他中枢神经系统淋巴瘤。

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