移植后淋巴增生性疾病(PTLD)表现为胆管阻塞

I. Morard, G. Mentha, L. Rubbia, S. Terraz, L. Spahr, A. Hadengue, P. Majno, P. Morel, E. Giostra
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引用次数: 1

摘要

成人肝移植(LT)后,移植后淋巴细胞增生性疾病(PTLD)是一种罕见但严重的并发症免疫抑制(IMS)存在急性或潜伏EBV感染。本病的临床表现具有特异性,肝移植后可能出现吻合口胆管狭窄。我们报告了2例成人患者,在OLT后3个月和8年,发生ebv相关的PTLD,并伴有弥漫性内生性胆管浸润,模拟吻合口胆道狭窄。在没有肝或肝门淋巴结累及的情况下,经皮活检是没有帮助的,诊断是通过手术活检。在减少IMS和利妥昔单抗治疗后,两例患者在诊断后5年和6年没有复发。综上所述,PTLD是OLT后胆道梗阻的鉴别诊断之一。诊断需要手术活检,治疗包括减少IMS和利妥昔单抗。
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Post Transplantation Lymphoproliferative Disorder (PTLD) Presenting as Biliary Duct Obstruction
After adult liver transplantation (LT), post-transplant lymphoproliferative disorder (PTLD) is an uncommon but serious complication of immunosuppression (IMS) in presence of an acute or latent EBV infection. The clinical pres- entation of this disease is aspecific, and, after LT, it may mimic anastomotic bile duct stricture. We report the cases of 2 adult patients who developed, 3 months and 8 years after OLT, an EBV-associated PTLD with diffuse intrinsic infiltration of bile duct mimicking anastomotic biliary stricture. In the absence of liver or hilar nodes in- volvement, percutaneous biopsies were non contributive and the diagnosis were made by surgical biopsy. After reduction of IMS and Rituximab treatment, both patients are alive without recurrence 5 and 6 years after diagnosis. In conclusion, PTLD is one of the differential diagnosis of biliary tree obstruction after OLT. Diagnosis requires surgical biopsies and treatment consists in IMS reduction and Rituximab.
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