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[一例肺毛霉菌病尸检病例,患者在急性髓细胞白血病缓解期因胸降主动脉破裂导致致命咯血]

[An autopsy case of pulmonary mucormycosis with fatal hemoptysis from a rupture of the thoracic descending aorta during remission from acute myelocytic leukemia].

作者信息

Izumi N, Kumagai H, Shindo T

机构信息

Department of Internal Medicine, Yamagata Prefectural Central Hospital.

出版信息

Rinsho Ketsueki. 2000 Nov;41(11):1201-7.

Abstract

A 16-year-old girl was hospitalized because of anemia and thrombocytopenia in April 1998, and was diagnosed as having AML (FAB:M2). After failure of initial remission induction therapy, she was successfully treated with the MEC regimen as a second-line chemotherapy. On June 22, the first consolidation therapy was started. One week later, the patient developed a high fever with backache. Chest computed tomography (CT) on July 8 showed a 3cm mass lesion adjacent to the thoracic descending aorta in the left upper lobe. She was given fluconazole and antibiotics, and remained in remission. On July 24, the mass lesion changed to a cavitary lesion on chest CT, suggesting a fungal infection, probably aspergillosis. With recovery from neutropenia, the patient became asymptomatic, and fluconazole was changed to itraconazole. On July 27, she suffered sudden, massive hemoptysis and died. Autopsy revealed a localized adhesion between the cavitary lesion and the thoracic descending aorta, and the aortic wall was ruptured at this site. Microscopic examination revealed invasion of mucormycotic hyphae into the wall of the aorta with infiltration of inflammatory cells. The vasa vasorum were occluded by thrombi, in which mucormycotic hyphae were detected.

摘要

1998年4月,一名16岁女孩因贫血和血小板减少症住院,被诊断为急性髓系白血病(FAB:M2)。初始缓解诱导治疗失败后,她作为二线化疗接受MEC方案治疗并获得成功。6月22日开始首次巩固治疗。一周后,患者出现高热伴背痛。7月8日的胸部计算机断层扫描(CT)显示左上叶降主动脉旁有一个3厘米的肿块病变。给予氟康唑和抗生素治疗,患者仍处于缓解状态。7月24日,胸部CT显示肿块病变变为空洞性病变,提示真菌感染,可能为曲霉菌病。随着中性粒细胞减少症的恢复,患者无症状,氟康唑改为伊曲康唑。7月27日,她突然大量咯血并死亡。尸检显示空洞性病变与降主动脉之间有局部粘连,主动脉壁在此处破裂。显微镜检查显示毛霉菌菌丝侵入主动脉壁并伴有炎症细胞浸润。滋养血管被血栓阻塞,在血栓中检测到毛霉菌菌丝。

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