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

机译:原发性肾上腺外胚NK / T细胞淋巴瘤:一个案例报告和文献综述

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摘要

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 of l-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:在他的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)。肝脏和肾上腺复发均鉴定丙二酸后2个月,其中临时施用L-天冬酰胺酶,导致完全代谢反应。然而,在中枢神经系统和致死淋巴瘤脑膜炎中的多重复发了连续发展。原发性肾上腺ENKL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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