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Primary adrenal extranodal NK/T-cell lymphoma: A case report and literature review

机译:原发性肾上腺外细胞NK / T细胞淋巴瘤:案例报告和文献综述

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A 37-year-old man was admitted to our department following the detection of bulky tumors in his bilateral adrenal glands. A biopsy resulted in the diagnosis of extranodal NK/T cell lymphoma, nasal type (ENKL). After debulking by chemotherapy, allogeneic hematopoietic stem cell transplantation (alloHCT) was performed. Relapses in the liver and adrenal glands were identified 2 months post alloHCT, for which temporary administration ofl-asparaginase resulted in complete metabolic response. However, multiple relapses in the central nervous system and lethal lymphomatous meningitis successively developed. Primary adrenal ENKL could tend to present as bulky lesion and follow an aggressive clinical course.
机译:在双侧肾上腺肿瘤中检测庞大的肿瘤后,一名37岁的男子被录取为我们的部门。 活组织检查导致诊断外骨NK / T细胞淋巴瘤,鼻型(ENK1)。 通过化疗储存后,进行同种异体造血干细胞移植(AllOhct)。 肝脏和肾上腺复发鉴定了丙二酸后2个月,其临时施用的副烷淀粉酶产生完全代谢反应。 然而,连续开发中枢神经系统和致死淋巴瘤脑膜炎的多重复发。 原发性肾上腺ENKL可能倾向于呈现庞大的病变并遵循侵略性的临床课程。

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