Ralaizanaka Behoavy Mahafaly, Razafindrazoto Chantelli Iamblaudiot, Bolot Eloïse, Bors Georges, Housson-Wetzel Stéphanie, Razafimahefa Soloniaina Hélio, Ramanampamonjy Rado Manitrala, Claude Pierre
Unity of Hepato-Gastroenterology, University Hospital Andrainjato, Fianarantsoa, Madagascar.
Unity of Gastroenterology, University Hospital Joseph Raseta Befelatanana, Antananarivo, Madagascar.
Clin Exp Gastroenterol. 2022 Aug 12;15:145-151. doi: 10.2147/CEG.S373728. eCollection 2022.
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.
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 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.
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.
毛霉菌病是一种罕见的系统性真菌感染,主要见于免疫功能低下的患者。它会导致体表和深部组织破坏,进而引起穿孔和出血。其以血管侵袭为特征的发病机制是局部梗死和血管血栓形成的根源。我们报告一例由胃肠道毛霉菌病引起的多发性胃溃疡、胃肠道出血和直肠穿孔病例。
一名75岁的II型糖尿病男性因急性腹痛伴大量便血入住重症监护病房。临床检查显示为急性腹膜炎和失血性休克状态。腹部和盆腔增强CT扫描显示直肠前壁穿孔。他立即接受了剖腹手术并进行了临时结肠造口术。多次上消化道内镜检查显示有多个胃溃疡病变。下消化道内镜检查显示直肠前表面有一个瘘口。胃活检的组织病理学显示急性和亚急性炎症改变,伴有提示毛霉菌病的丝状成分。直肠活检的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显示为 菌株。抗真菌药敏试验报告对脂质体两性霉素B敏感。该II型糖尿病患者被诊断为胃肠道毛霉菌病引起的多发性胃溃疡、直肠穿孔和肺栓塞。在接受脂质体两性霉素B治疗6周并结合临时结肠造口术和适当的糖尿病管理后,预后良好。
胃肠道毛霉菌病仍然是一个多学科的诊断挑战,在临床实践中较少见,诊断过程漫长。这种机会性系统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。如果早期进行药物和手术治疗,胃肠道毛霉菌病预后良好。