移植后淋巴细胞增生性疾病,表现为大肠梗阻,导致分布性休克。

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Amy Wang, Brendan Flynn, Mary O'Donnell, Rathnayaka Mudiyanselage Kalpanee Dhanushika Gunasingha
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引用次数: 0

摘要

一位70多岁有肝移植史的女性,以便秘和白细胞增多症为主要表现。影像学显示一个大的阻塞乙状结肠肿块。她做了结肠镜检查,发现肠腔狭窄但没有肿块。她接受了介入放射学指导下的肿块活检。术后,她出现心动过速和低血压。她被带到手术室,发现活检部位出血。出血得到控制,她接受了转移横向环形结肠造口术。术后,她出现了分配性休克,尽管采取了复苏措施,但仍有进展。她的病理为Epstein-Barr病毒阳性的移植后单形态淋巴细胞增生性疾病(PTLD)弥漫性大b细胞淋巴瘤型。弥散性休克是由淋巴瘤继发的大量细胞因子释放引起的,因此她开始接受紧急化疗方案。尽管如此,她的血流动力学从未恢复,她被同情地拔管。PTLD的临床表现是多变的,可以迅速发展到危及生命的表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Post-transplant lymphoproliferative disorder presenting as large bowel obstruction leading to distributive shock.

A woman in her 70s with a history of liver transplantation presented with constipation and leucocytosis. Imaging demonstrated a large obstructing sigmoid mass. She underwent a colonoscopy that showed narrowing but no luminal mass. She underwent an interventional radiology guided biopsy of the mass. Post-procedurally, she developed tachycardia and hypotension. She was taken to the operating room and was found to be haemorrhaging from the biopsy sites. The haemorrhage was controlled, and she underwent a diverting transverse loop colostomy. Postoperatively, she developed distributive shock that progressed despite resuscitative efforts. Her pathology returned as Epstein-Barr virus positive monomorphic post-transplant lymphoproliferative disorder (PTLD) of diffuse large B-cell lymphoma type. The distributive shock was from massive cytokine release secondary to her lymphoma, so she was started on an urgent chemotherapy regimen. Despite this, she never recovered haemodynamically, and she was compassionately extubated. The clinical presentation of PTLD can be variable with rapidly progressing life-threatening manifestations.

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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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