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伴有致命性大量咯血的肺毛霉病

Pulmonary mucormycosis with fatal massive hemoptysis.

作者信息

Harada M, Manabe T, Yamashita K, Okamoto N

机构信息

Department of Pathology, Kawasaki Medical School, Kurashiki, Japan.

出版信息

Acta Pathol Jpn. 1992 Jan;42(1):49-55. doi: 10.1111/j.1440-1827.1992.tb01110.x.

Abstract

A case of pulmonary mucormycosis in a 57-year-old woman with acute promyelocytic leukemia (APL) who died of massive hemoptysis is reported. Chest radiography revealed changes that began with a small focal infiltration and progressed to a large round nodule with cavity formation. Postmortem examination showed the nodule to be composed mainly of infarcted lung tissue with saprophytic growth of Mucor. An adjacent proximal branch of the left pulmonary artery was thrombosed with mucoraceous hyphae, and it had ruptured into the cavitary space around the necrotic tissue and then into a conducting bronchus. In general, both fatal massive hemoptysis and cavity formation are rare in pulmonary mucormycosis. In our present case, the histological findings suggested that both phenomena were closely related to the pulmonary infarction caused by Mucor invasion of the pulmonary artery.

摘要

报告了一例57岁急性早幼粒细胞白血病(APL)女性患者发生肺毛霉病,该患者死于大量咯血。胸部X线检查显示病变始于小片状局灶性浸润,进展为伴有空洞形成的大圆形结节。尸检显示该结节主要由梗死的肺组织组成,伴有毛霉腐生生长。左肺动脉的一个相邻近端分支被毛霉样菌丝血栓形成,并且已破裂进入坏死组织周围的空洞空间,然后进入一个传导支气管。一般来说,致命性大量咯血和空洞形成在肺毛霉病中都很罕见。在我们目前的病例中,组织学结果表明这两种现象都与毛霉侵犯肺动脉导致的肺梗死密切相关。

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