Surgical treatment of appendiceal mucormycosis in an immunocompromised patient: a case report.

IF 0.7 Q4 SURGERY
Yukiya Orihara, Shingo Kurahashi, Katsuhiko Kamei, Kazuhiro Hiramatsu
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Abstract

Background: Gastrointestinal mucormycosis is a rapidly progressing and often fatal disease, predominantly affecting immunocompromised patients. Surgical intervention, in addition to antifungal therapy, is essential. Herein, we describe the successful management of appendiceal mucormycosis in a patient with acute promyelocytic leukemia through rapid surgical intervention and antifungal therapy.

Case presentation: A 29-year-old woman underwent autologous peripheral blood stem cell transplantation for acute promyelocytic leukemia (APL). Subsequently, her condition relapsed, and remission induction therapy was initiated. During the immunosuppressive period, she developed a fever and severe abdominal pain. Computed tomography revealed severe edema of the ileum, cecum, and ascending colon. Despite receiving multiple antibiotics, antivirals, and antifungals, her condition showed no improvement. Consequently, she underwent exploratory laparotomy, with no bowel perforation noted, revealing severe inflammation in the ileum, cecum, and ascending colon, as well as appendiceal necrosis. Appendectomy was performed, and histopathological analysis revealed hyphae in the vessels and layers of the appendiceal wall, suggestive of mucormycosis. The patient was diagnosed with appendiceal mucormycosis, and liposomal amphotericin B was administered. Subsequent monitoring showed no recurrence of mucormycosis. Genetic analysis of the resected tissue revealed Rhizopus microspores as the causative agent.

Conclusions: Rapid surgical intervention and antifungal drug administration proved successful in managing appendiceal mucormycosis in a patient with APL. Early recognition and aggressive surgical intervention are imperative to improve outcomes in such patients.

一名免疫力低下患者阑尾粘液瘤病的手术治疗:病例报告。
背景:胃肠道粘孢子菌病是一种进展迅速、往往致命的疾病,主要影响免疫力低下的患者。除了抗真菌治疗外,手术干预也是必不可少的。在此,我们描述了一名急性早幼粒细胞白血病患者通过快速手术干预和抗真菌治疗成功治愈阑尾粘液瘤病的病例:一名 29 岁的女性因急性早幼粒细胞白血病(APL)接受了自体外周血干细胞移植。随后,她的病情复发,并开始接受缓解诱导治疗。在免疫抑制期间,她出现了发烧和剧烈腹痛。计算机断层扫描显示回肠、盲肠和升结肠严重水肿。尽管她接受了多种抗生素、抗病毒药物和抗真菌药物治疗,但病情仍不见好转。因此,她接受了探查性开腹手术,在没有发现肠穿孔的情况下,发现回肠、盲肠和升结肠有严重炎症,阑尾也出现坏死。对患者进行了阑尾切除术,组织病理学分析显示,阑尾壁的血管和各层均有菌丝,提示为粘孢子菌病。患者被诊断为阑尾粘液瘤病,并服用了两性霉素 B 脂质体。随后的监测显示,粘液瘤病没有复发。对切除组织的基因分析显示,小孢子根霉菌是致病菌:事实证明,快速手术干预和抗真菌药物治疗成功地控制了一名 APL 患者的阑尾粘液瘤病。要改善此类患者的预后,早期识别和积极手术干预势在必行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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