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儿童急性淋巴细胞白血病患者合并鼻脑型毛霉菌病和新型近平滑念珠菌菌血症:一种罕见的合并感染。

Rhinocerebral mucormycosis and Trichosporon asahii fungemia in a pediatric patient with acute lymphoblastic leukemia: a rare coinfection.

机构信息

Guangxi Academy of Medical Sciences, The People's Hospital of Guangxi Zhuang Autonomous Region, Department of Laboratory Medicine, Nanning, Guangxi, China.

Guangxi Academy of Medical Sciences, The People's Hospital of Guangxi Zhuang Autonomous Region, Department of Pediatrics, Nanning, Guangxi, China.

出版信息

Rev Inst Med Trop Sao Paulo. 2024 Jul 8;66:e41. doi: 10.1590/S1678-9946202466041. eCollection 2024.

Abstract

Mucormycosis is a rare life-threatening opportunistic infection, with rhinocerebral mucormycosis (ROCM) being the most common presentation. Trichosporon asahii is an emerging pathogen that often causes fatal infections in patients with underlying hematologic malignancies due to its high drug resistance. We report a rare case of concomitant rhinocerebral mucormycosis and T. asahii fungemia secondary to Pseudomonas aeruginosa sepsis in a patient with neutropenia and acute lymphoblastic leukemia. A boy aged one year and two months was diagnosed with B-cell acute lymphoblastic leukemia on January 10 and underwent three courses of regular chemotherapy. He experienced neutropenia for 154 days and was hospitalized for vomiting, diarrhea and fever for 3 days. The day after hospitalization, Pseudomonas aeruginosa was isolated by blood culture and ceftazidime/avibactam was administered. Extracorporeal Membrane Oxygenation (ECMO) was used to provide continuous extracorporeal respiration and circulation for the patient. On day 8, the patient developed T. asahii fungemia. On day 10, he presented with necrotizing skin caused by Rhizopus delemar. He was treated with liposomal amphotericin B for Rhizopus delemar and voriconazole for T. asahii infection. Unfortunately, his health deteriorated and he died on day 11 due to the rapid progression of the infection and multiple organ failure. The management and treatment of such a complex infection requires a multidisciplinary approach and close monitoring of the patient's condition. Therefore, it is imperative to continue to research and report rare cases such as this to further understand the complexities of mucormycosis and trichosporidiosis coinfection and improve patient outcomes.

摘要

毛霉菌病是一种罕见的危及生命的机会性感染,其中鼻脑毛霉菌病(ROCM)最为常见。近平滑念珠菌是一种新兴的病原体,由于其高度耐药性,常导致患有潜在血液恶性肿瘤的患者发生致命感染。我们报告了一例罕见的中性粒细胞减少症和急性淋巴细胞白血病患者继发于铜绿假单胞菌败血症的同时发生鼻脑毛霉菌病和近平滑念珠菌菌血症的病例。一名 1 岁零 2 个月的男孩于 1 月 10 日被诊断为 B 细胞急性淋巴细胞白血病,并接受了三疗程常规化疗。他经历了 154 天的中性粒细胞减少症,并因呕吐、腹泻和发热住院 3 天。住院的第二天,血培养分离出铜绿假单胞菌,并给予头孢他啶/阿维巴坦治疗。体外膜氧合(ECMO)用于为患者提供持续的体外呼吸和循环。第 8 天,患者发生近平滑念珠菌菌血症。第 10 天,他出现由 Rhizopus delemar 引起的坏死性皮肤病变。他接受了脂质体两性霉素 B 治疗 Rhizopus delemar 和伏立康唑治疗 T. asahii 感染。不幸的是,他的健康状况恶化,由于感染迅速进展和多器官衰竭,于第 11 天死亡。这种复杂感染的管理和治疗需要多学科方法和密切监测患者的病情。因此,继续研究和报告此类罕见病例对于进一步了解毛霉菌病和曲霉菌病合并感染的复杂性并改善患者预后至关重要。

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