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双侧肺移植术后血管侵袭性曲霉病导致的多灶性肠穿孔:一例报告并文献复习

Multifocal bowel perforation from angioinvasive aspergillosis after bilateral lung transplantation: a case report and review of the literature.

作者信息

Kerlee Kacie, Ehab Jasmina, Watson Jeremy, Weill Patrick, Chandra Raghav, Keshavamurthy Suresh, Mehta Ankeeta, Shoultz Thomas H

机构信息

Division of Burns, Trauma, Acute and Critical Care Surgery, Department of Surgery, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Division of Pulmonology and Critical Care Medicine, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.

出版信息

AME Case Rep. 2025 Jul 15;9:91. doi: 10.21037/acr-24-221. eCollection 2025.

Abstract

BACKGROUND

Lung transplant recipients on immunosuppression are at increased risk for aggressive opportunistic infections, including invasive aspergillosis (IA). Distal septic embolization from angio-IA with involvement of the small and large bowel is extremely uncommon, and clinical manifestations of bowel ischemia and perforation may be masked due to immunosuppression.

CASE DESCRIPTION

We present herein the first reported case of peritonitis secondary to jejunal and cecal perforation secondary to angio-IA after lung transplantation (LT) in a 62-year-old male. The patient was admitted to the hospital for acute cellular rejection requiring high-dose immunosuppression. His course was complicated by respiratory failure secondary to IA, with resulting multiorgan system dysfunction during which time peritonitis was noted on examination and cross-sectional imaging demonstrated pneumatosis, portal venous gas, and pneumoperitoneum. The patient required emergent surgical intervention and underwent an exploratory laparotomy, jejunal resection, right hemicolectomy, and end ileostomy with colonic mucus fistula. Final pathologic analysis of resected specimens demonstrated angio-IA in both the jejunal and cecal segments with associated transmural ischemic necrosis.

CONCLUSIONS

Bowel perforation secondary to angio-IA is a very rare but serious complication after LT that is associated with high morbidity and mortality. Evaluation requires a high index of suspicion in the setting of immunosuppression and often concomitant extraintestinal pathologies. Early, aggressive surgical intervention is necessary.

摘要

背景

接受免疫抑制治疗的肺移植受者发生侵袭性机会性感染(包括侵袭性曲霉病,IA)的风险增加。血管侵袭性曲霉病导致的远端脓毒性栓塞累及小肠和大肠极为罕见,且由于免疫抑制,肠道缺血和穿孔的临床表现可能被掩盖。

病例描述

我们在此报告首例62岁男性肺移植(LT)后因血管侵袭性曲霉病继发空肠和盲肠穿孔导致腹膜炎的病例。该患者因急性细胞排斥反应入院,需要大剂量免疫抑制治疗。其病程因侵袭性曲霉病继发呼吸衰竭而复杂化,导致多器官系统功能障碍,在此期间检查发现腹膜炎,横断面成像显示存在肠壁积气、门静脉积气和气腹。患者需要紧急手术干预,接受了剖腹探查、空肠切除、右半结肠切除及末端回肠造口术并伴有结肠黏液瘘。切除标本的最终病理分析显示空肠和盲肠段均存在血管侵袭性曲霉病,并伴有透壁性缺血坏死。

结论

血管侵袭性曲霉病继发肠穿孔是肺移植后一种非常罕见但严重的并发症,与高发病率和死亡率相关。在免疫抑制及常伴有肠外病变的情况下,评估需要高度怀疑。早期积极的手术干预是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45b8/12319623/c51f97734622/acr-09-24-221-f1.jpg

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