胃肠道粘液霉菌病引起的大量下消化道出血、直肠穿孔和肺栓塞:一个病例报告的漫长诊断途径。

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY
Clinical and Experimental Gastroenterology Pub Date : 2022-08-12 eCollection Date: 2022-01-01 DOI:10.2147/CEG.S373728
Behoavy Mahafaly Ralaizanaka, Chantelli Iamblaudiot Razafindrazoto, Eloïse Bolot, Georges Bors, Stéphanie Housson-Wetzel, Soloniaina Hélio Razafimahefa, Rado Manitrala Ramanampamonjy, Pierre Claude
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引用次数: 0

摘要

毛霉病是一种罕见的全身性真菌感染,主要见于免疫功能低下的患者。它负责表面和深层组织破坏,导致穿孔和出血。其发病机制以血管侵犯为代表,起源于局部梗死和血管血栓形成。我们报告一例胃肠道(GI)粘液霉菌病引起的多发性胃溃疡,胃肠道出血和直肠穿孔。病例介绍:一名75岁男性,患有II型糖尿病,因急性腹痛合并大量便血被送入重症监护病房。临床检查为急性腹膜炎,失血性休克状态。腹部及盆腔CT扫描及静脉造影剂显示直肠前壁穿孔。他立即接受了剖腹手术和临时结肠造口术。多次上消化道内镜检查显示多发性胃溃疡病变。下消化道内窥镜显示直肠前表面有瘘口。胃活检的组织病理学显示急性和亚急性炎症改变,丝状成分提示毛霉病。直肠活检组织病理学显示为亚急性非特异性炎症。直肠瘘口分泌物培养为根霉菌。抗真菌药敏试验报告对两性霉素b脂质体敏感。保留了II型糖尿病患者胃肠道粘液霉菌病引起的多发性胃溃疡、直肠穿孔和肺栓塞的诊断。两性霉素B脂质体治疗6周后,伴有临时结肠造口术和适当的糖尿病管理,结果良好。结论:胃肠道毛霉病仍然是一个多学科的诊断挑战,在临床实践中较少出现,诊断途径较长。这种机会性全身性真菌病可导致许多胃肠道并发症,包括穿孔,大量胃肠道出血,甚至多种胃肠道外并发症。如果早期通过药物和手术治疗,胃肠道毛霉菌病有良好的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Gastrointestinal Mucormycosis-Induced Massive Lower Gastrointestinal Bleeding, Rectal Perforation, and Pulmonary Embolism: A Long Diagnostic Pathway in a Case Report.

Gastrointestinal Mucormycosis-Induced Massive Lower Gastrointestinal Bleeding, Rectal Perforation, and Pulmonary Embolism: A Long Diagnostic Pathway in a Case Report.

Gastrointestinal Mucormycosis-Induced Massive Lower Gastrointestinal Bleeding, Rectal Perforation, and Pulmonary Embolism: A Long Diagnostic Pathway in a Case Report.

Gastrointestinal Mucormycosis-Induced Massive Lower Gastrointestinal Bleeding, Rectal Perforation, and Pulmonary Embolism: A Long Diagnostic Pathway in a Case Report.

Introduction: Mucormycosis is a rare systemic fungal infection, mainly observed in immunocompromised patients. It is responsible for surface and deep tissue destruction leading to perforations and hemorrhage. Its pathogenesis represented by an angio-invasion is at the origin of a local infarction and a vascular thrombosis. We report a case of gastrointestinal (GI) mucormycosis-induced multiple gastric ulcers, GI bleeding and rectal perforation.

Case presentation: A 75-year-old man, with type II diabetes mellitus, was admitted to the intensive care unit for an acute abdominal pain associated with massive hematochezia. Clinical examination was that of an acute peritonitis and a hemorrhagic shock state. Abdominal and pelvic CT scan with intravenous contrast concluded to a perforation of the anterior wall of the rectum. He underwent immediate laparotomy with temporary colostomy. Several upper GI endoscopies had shown multiple gastric ulcer lesions. Lower GI endoscopy showed a fistulous orifice of the rectum on its anterior surface. Histopathology of the gastric biopsy showed acute and subacute inflammatory changes with filamentous elements suggesting mucormycosis. Histopathology of the rectal biopsy showed a subacute non-specific inflammation. Culture of the secretions from the rectal fistula orifice showed the strain Rhizopus sp. Antifungal susceptibility testing reported sensitivity to liposomal amphotericin B. The diagnosis of GI mucormycosis-induced multiple gastric ulcers, rectal perforation and pulmonary embolism in the patient with type II diabetes mellitus was retained. The outcomes were favorable after 6 weeks of treatment with liposomal amphotericin B associated with temporary colostomy and appropriate diabetes management.

Conclusion: GI mucormycosis remains a multidisciplinary diagnostic challenge, less frequent in clinical practice, with a long diagnostic pathway. This opportunistic systemic mycosis can lead to numerous GI complications including perforation, massive GI bleeding and even multiple extra-GI complications. GI mucormycosis has a good prognosis if it is treated early with medical and surgical treatment.

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来源期刊
Clinical and Experimental Gastroenterology
Clinical and Experimental Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
5.10
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0.00%
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26
审稿时长
16 weeks
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