Post-renal transplant plasma cell dyscrasia presenting as retroperitoneal plasmacytoma: A case report and literature review

Mahvish Muzaffar MD, Rekha Chaudhary MD, Xin Li MD, Shobha Ratnam MD
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引用次数: 1

Abstract

Post-transplant lymphoproliferative disease (PTLD) is a rare but potentially fatal complication of organ transplanta-tion. Most cases of PTLD represent Epstein Barr virus (EBV)-related B-cell disease in a setting of pharmacological immunosuppression. Post-transplant plasma cell dyscrasia is very rare, and post-transplant plasma cell dyscrasia with extramedullary plasmacytoma is extremely rare. We report here a case of the latter, which to our knowledge is the fourth such reported case in the English literature. A 22-year-old man developed post-transplant plasma cell dyscrasia 20 years after a renal transplant while on immunosuppression. His presentation included retroperitoneal plasmacytoma, which is very rare and is probably the first case in a renal transplant patient. The patient is in complete remission 1 year after receiving five cycles of bortezomib and dexamethasone.

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肾移植后浆细胞增生表现为腹膜后浆细胞瘤:1例报告及文献复习
移植后淋巴细胞增生性疾病(PTLD)是一种罕见但可能致命的器官移植并发症。大多数PTLD病例代表eb病毒(EBV)相关的b细胞疾病在药理学免疫抑制的设置。移植后浆细胞增生非常罕见,移植后浆细胞增生合并髓外浆细胞瘤更是极为罕见。我们在这里报告了后者的一个病例,据我们所知,这是在英语文献中报告的第四个这样的病例。一名22岁的男性在接受免疫抑制治疗20年后发生肾移植后浆细胞病变。他的报告包括腹膜后浆细胞瘤,这是非常罕见的,可能是第一例肾移植患者。患者在接受5个疗程的硼替佐米和地塞米松治疗后1年完全缓解。
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来源期刊
Dialysis & Transplantation
Dialysis & Transplantation 医学-工程:生物医学
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