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肺移植受者的淋巴增殖性疾病。

Lymphoproliferative disorder in a lung transplant recipient.

作者信息

Haji Hassan A, Corwin Douglas S, So Jennifer Y, Reed Robert M

机构信息

Pulmonary and Critical Care Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.

Pulmonary and Critical Care Medicine, St Luke's University Health Network, Bethlehem, Pennsylvania, USA.

出版信息

BMJ Case Rep. 2020 Mar 31;13(3):e234532. doi: 10.1136/bcr-2020-234532.

Abstract

Post-transplantation lymphoproliferative disorder (PTLD) is uncommon following solid organ transplantation. We present a case of PTLD presenting as hematochezia and abdominal pain in a 66-year-old man, who had undergone bilateral lung transplantation with alemtuzumab induction 7 months prior to presentation. The transplant serologic status was "high-risk" for the presence of both Epstein-Barr virus (EBV) serologies in the donor and negative serologies in the recipient. Biopsies taken during colonoscopy stained strongly positive for EBV-encoded RNA. Mediastinal lymph node biopsies also showed atypical, EBV-positive lymphohistiocytic infiltration with focal necrosis. The patient's hospital course was complicated by treatment side effects, most notably bowel perforation following rituximab. In this case report the topic of PTLD is reviewed and consideration is given to whether alemtuzumab induction may have contributed to the patient's development of PTLD.

摘要

实体器官移植后发生移植后淋巴细胞增生性疾病(PTLD)并不常见。我们报告一例66岁男性患者,以便血和腹痛为表现的PTLD,该患者在出现症状前7个月接受了阿仑单抗诱导的双侧肺移植。就供体中EB病毒(EBV)血清学检测均为阳性而受体血清学检测为阴性而言,该移植血清学状态属于“高危”。结肠镜检查时所取活检标本经EBV编码RNA染色呈强阳性。纵隔淋巴结活检也显示非典型的、EBV阳性的淋巴组织细胞浸润伴局灶性坏死。该患者的住院病程因治疗副作用而复杂化,最显著的是利妥昔单抗治疗后出现肠穿孔。在本病例报告中,对PTLD主题进行了回顾,并探讨了阿仑单抗诱导是否可能促使该患者发生PTLD。

相似文献

1
Lymphoproliferative disorder in a lung transplant recipient.肺移植受者的淋巴增殖性疾病。
BMJ Case Rep. 2020 Mar 31;13(3):e234532. doi: 10.1136/bcr-2020-234532.

本文引用的文献

9
Five-year outcomes with alemtuzumab induction after lung transplantation.肺移植后用阿仑单抗诱导治疗的 5 年结果。
J Heart Lung Transplant. 2011 Jul;30(7):743-54. doi: 10.1016/j.healun.2011.01.714. Epub 2011 Mar 21.

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