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[三房心——肺含铁血黄素沉着症的罕见病因]

[Cor triatriatum--a rare cause of pulmonary hemosiderosis].

作者信息

Dieckmann H J, Chares M

机构信息

Abt. Innere Medizin II, Ev. Krankenhaus Unna.

出版信息

Pneumologie. 1995 Aug;49(8):475-9.

PMID:7479643
Abstract

Pneumological examinations including open lung biopsy performed on a male patient of 30 years of age suffering from severe respiratory distress that disabled him, as well as from massive recurring attacks of hemoptysis, resulted in suspicion of idiopathic pulmonary hemosiderosis (also known as Ceelen-Gellerstedt's syndrome). Diagnosis of cor triatriatum followed by surgery was arrived at only after a pulmonary oedema had developed and after other rare cardiac diseases had been considered. This rare congenital malformation--which occasionally becomes clinically manifest only in the adult--should be suspected in differential diagnosis of respiratory distress and a sometimes also life-threatening hemoptysis. Echocardiography is the diagnostic method of choice in this regard.

摘要

对一名30岁男性患者进行了包括开胸肺活检在内的肺部检查。该患者患有严重的呼吸窘迫,导致身体残疾,还伴有大量反复咯血。检查结果怀疑为特发性肺含铁血黄素沉着症(也称为塞伦-格勒斯泰德综合征)。仅在出现肺水肿并排除其他罕见心脏疾病后,才诊断为三房心并进行了手术。这种罕见的先天性畸形——偶尔仅在成年期才出现临床症状——在鉴别诊断呼吸窘迫以及有时同样危及生命的咯血时应予以怀疑。在这方面,超声心动图是首选的诊断方法。

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