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[青少年肺动静脉瘘]

[Pulmonary arteriovenous fistula in an adolescent].

作者信息

Zoricić-Letoja I, Mikulić Z, Simunić S, Vladović-Relja T, Krizanac S

机构信息

Bolnica za tuberkulozu pluća i plućne bolesti djece i mladezi, Zagreb.

出版信息

Lijec Vjesn. 1995 Jan-Feb;117(1-2):28-32.

PMID:7651067
Abstract

We report the case of a patient, a 19-year-old young man, with a rare malformation of the pulmonary blood vessels--a complex arteriovenous (A-V) fistula. The disease was characterized by typical signs of the right-to-left shunt: cyanosis, clubbed fingers and exertional dyspnea. Hypoxemia and polyglobulia were present in the blood examination findings and functional tests showed significantly reduced diffusion lung capacity and progressive dyspnea, while ergometry revealed cyanosis. The physical examination, ECG and ultrasound of the heart were normal as well as aortography. The final diagnosis was made by pulmonary angiography which showed a complex A-V malformation of several feeding arteries and profuse initial multiple venous drainage. Following a successful surgical procedure the diagnosis was also confirmed histopathologically-diffuse teleangiectatic A-V fistula of the lower lobe of the left lung. Following surgery cyanosis, dyspnea, hypoxemia and polyglobulia disappeared and the young man has been well for the following two years.

摘要

我们报告了一例患者,一名19岁的年轻男性,患有罕见的肺血管畸形——复杂动静脉(A-V)瘘。该疾病的特征为典型的右向左分流体征:发绀、杵状指和劳力性呼吸困难。血液检查结果显示存在低氧血症和红细胞增多症,功能测试显示肺弥散能力显著降低且进行性呼吸困难,而运动试验显示发绀。体格检查、心电图、心脏超声以及主动脉造影均正常。最终诊断通过肺血管造影做出,显示有几条供血动脉的复杂A-V畸形以及大量起始的多处静脉引流。成功手术后,组织病理学也证实了诊断——左肺下叶弥漫性毛细血管扩张性A-V瘘。手术后,发绀、呼吸困难、低氧血症和红细胞增多症消失,该年轻人在接下来的两年里情况良好。

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[Pulmonary arteriovenous fistula].
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