Primary invasive gastric mucormycosis presenting as meleney's gangrene: A case report and review of literature

M. Safwan, S. Khan, A. Belthazar, M. Sasidharan
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Abstract

Mucormycosis is an uncommon but potentially lethal fungal infection in immunocompromised individuals. The natural history of the disease is vascular invasion followed by thrombosis and necrosis of infected tissues. It can affect any organ system. Gastrointestinal (GI) mucormycosis is quite rare. Here, we report a case of primary invasive gastric mucormycosis in a 45-year-old male with diabetes and ethanol-related chronic liver disease who presented with necrotizing fascitis of the left thigh, groin, and lower abdominal wall. At presentation, he was hemodynamically unstable, anuric, and febrile with a high blood glucose level. He was stabilized with aggressive debridement and critical care management. During hospitalization, he developed sudden episode of upper GI bleed. Gastroscopy revealed extensive ulcerations with thick mucus in the fundus and body of the stomach. Biopsy from the lesions and special stain examination was consistent with invasive gastric mucormycosis. Delayed presentation of our patient and rapid progression to fungemia resulted in mortality.
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原发性侵袭性胃粘膜真菌病表现为meleney坏疽:1例报告及文献复习
毛霉病是一种罕见的,但潜在致命的真菌感染免疫功能低下的个人。本病的自然病程是血管侵入,继之以感染组织的血栓和坏死。它可以影响任何器官系统。胃肠道(GI)毛霉菌病是相当罕见的。在这里,我们报告一例原发性侵袭性胃粘膜真菌病,患者为45岁男性,患有糖尿病和酒精相关的慢性肝病,表现为左大腿、腹股沟和下腹壁的坏死性筋膜炎。入院时,患者血流动力学不稳定,无尿,发热伴高血糖。通过积极清创和重症监护管理,患者病情稳定。住院期间,他突然出现上消化道出血。胃镜检查显示胃底和胃体有广泛的溃疡和粘稠的粘液。病变活检和特殊染色检查符合侵袭性胃粘膜真菌病。我们的病人的延迟表现和快速进展到真菌血症导致死亡。
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