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侵袭性胃肠道毛霉病表现为中性粒细胞减少性小肠结肠炎:一例报告

Invasive Gastrointestinal Mucormycosis Presenting as Neutropenic Enterocolitis: A Case Report.

作者信息

AlBassam Hamad J, Alanazi Wael, Al Rashid Faisal, Alruwaii Zainab I, Almusa Zainab

机构信息

Department of Medicine, Infectious Disease Section, King Fahad Specialist Hospital, Dammam, Saudi Arabia.

Department of Hematology, King Fahad Specialist Hospital, Dammam, Saudi Arabia.

出版信息

Am J Case Rep. 2025 Sep 8;26:e948878. doi: 10.12659/AJCR.948878.

Abstract

BACKGROUND Gastrointestinal mucormycosis is an underrecognized and underreported fungal infection with a high mortality rate. Diagnosis is often confounded by a non-specific constellation of signs and symptoms. We present a case of neutropenic colitis and ileocecal perforation secondary to gastrointestinal mucormycosis. CASE REPORT The patient was a 19-year-old man recently diagnosed with B-cell acute lymphoblastic leukemia, on active chemotherapy. He presented with abdominal pain and tenderness, and a contrast-enhanced CT revealed neutropenic colitis. Despite broad-spectrum antibiotics, his condition worsened, prompting reassessment. Follow-up CT showed bowel ischemia and a pelvic collection. He underwent an emergency laparotomy, which revealed destruction of the anterior cecal wall and detachment from the terminal ileum and ascending colon. Ileocecal resection was performed and histopathologic examination demonstrated angioinvasive fungal elements consistent with Mucor spp. He was diagnosed with gastrointestinal mucormycosis and promptly started on amphotericin intravenously. He improved over the next 2 weeks and was discharged with a plan to continue his 6-week course as an outpatient, followed by oral posaconazole maintenance therapy. Several weeks later, his infection relapsed secondary to non-compliance. He underwent repeat surgical debridement and antimicrobial therapy was restarted with intravenous amphotericin and Isavuconazole. He successfully completed 6 weeks of treatment and was transitioned to oral Isavuconazole prophylaxis. He remained stable and relapse-free at 6 months following his second procedure. CONCLUSIONS The case highlights the importance of early recognition of patients at risk for this infection, maintaining a high index of suspicion, and employing aggressive medical and surgical management strategies to avoid mortality.

摘要

背景 胃肠道毛霉菌病是一种未得到充分认识和报告的真菌感染,死亡率很高。诊断常常因一系列非特异性的体征和症状而混淆。我们报告一例继发于胃肠道毛霉菌病的中性粒细胞减少性结肠炎和回盲部穿孔病例。病例报告 患者为一名19岁男性,最近被诊断为B细胞急性淋巴细胞白血病,正在接受积极化疗。他出现腹痛和压痛,增强CT显示中性粒细胞减少性结肠炎。尽管使用了广谱抗生素,他的病情仍恶化,促使重新评估。后续CT显示肠缺血和盆腔积液。他接受了急诊剖腹手术,术中发现盲肠前壁破坏,与回肠末端和升结肠分离。进行了回盲部切除术,组织病理学检查显示血管侵袭性真菌成分,符合毛霉属。他被诊断为胃肠道毛霉菌病,并立即开始静脉注射两性霉素。在接下来的2周里他病情好转并出院,计划作为门诊患者继续进行为期6周的疗程,随后进行口服泊沙康唑维持治疗。几周后,由于不依从,他的感染复发。他接受了再次手术清创,并重新开始使用静脉注射两性霉素和艾沙康唑进行抗菌治疗。他成功完成了6周的治疗,并转为口服艾沙康唑预防。在第二次手术后6个月,他保持稳定且未复发。结论 该病例强调了早期识别这种感染高危患者、保持高度怀疑指数以及采用积极的药物和手术管理策略以避免死亡的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a0/12427590/47f36deb257e/amjcaserep-26-e948878-g001.jpg

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