Post-Transplant Lymphoproliferative Disorder at the Porta Hepatis Causing Hepatic Artery Stenosis and Cholestasis.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL American Journal of Case Reports Pub Date : 2025-01-23 DOI:10.12659/AJCR.945837
Badi Rawashdeh, Christina Papageorge, Yazan Al-Adwan
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Abstract

BACKGROUND Post-transplant lymphoproliferative disorder (PTLD) encompasses a group of disorders ranging from hyperplastic to malignant lymphoid proliferations in the post-transplant period owing to immunosuppression, often in the setting of EBV transformation. PTLD is a rare complication of immunosuppression that, like lymphomas, can have a variable presentation based on disease localization. We report a case of PTLD mass effect at the porta hepatis for the first time in the literature, resulting in hepatic artery stenosis (HAS) and common hepatic duct obstruction. CASE REPORT A 54-year-old woman presented with cholestasis 4 months after receiving a deceased donor liver transplant. MRCP revealed a mass at the porta hepatis causing biliary compression, which resolved with subsequent biliary stenting. The woman presented again 3 weeks later with a similar presentation. CT revealed that the mass had enlarged, causing HAS, which resolved with subsequent hepatic artery stenting. The biopsy revealed PTLD, and the patient was successfully managed with rituximab and a reduction of her immunosuppressive regimen. CONCLUSIONS This case report describes a rare occurrence of PTLD, which particularly impacting the porta hepatis, resulting in HAS and compression of the bile duct. PTLD should be considered in the differential diagnosis for obstructive jaundice and hepatic artery compression, even in the early post-transplant months, when these symptoms are often attributed to surgical factors.

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肝门移植后淋巴细胞增生性疾病引起肝动脉狭窄和胆汁淤积。
移植后淋巴细胞增生性疾病(PTLD)包括移植后由于免疫抑制引起的增生到恶性淋巴细胞增生等一系列疾病,通常发生在EBV转化的背景下。PTLD是一种罕见的免疫抑制并发症,像淋巴瘤一样,可以根据疾病的定位有不同的表现。我们在文献中首次报道一例PTLD在肝门的肿块效应,导致肝动脉狭窄(HAS)和肝总管阻塞。病例报告一名54岁妇女在接受已故供体肝移植4个月后出现胆汁淤积。MRCP显示肝门肿块引起胆道压迫,随后胆道支架置入解决。三周后,该妇女再次出现类似的症状。CT显示肿块肿大,引起HAS,随后行肝动脉支架置入术。活检显示PTLD,患者成功地用利妥昔单抗治疗,并减少了免疫抑制方案。结论本病例报告描述了一种罕见的PTLD,特别是影响肝门,导致HAS和胆管压迫。在梗阻性黄疸和肝动脉压迫的鉴别诊断中,即使在移植后的最初几个月,当这些症状通常归因于手术因素时,也应考虑PTLD。
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American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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