Clinical characteristics and postoperative outcomes of systemic artery-to-pulmonary vessel fistula in hemoptysis patients

Author(s):  
Chu-Jie Zhang ◽  
Fa-Ming Jiang ◽  
Ze-Jin Zuo ◽  
Shan-Shan Li ◽  
Yue-An Zhao ◽  
...  
1974 ◽  
Vol 68 ◽  
pp. 137-141 ◽  
Author(s):  
R. Visconti ◽  
E. Maña ◽  
C. Quiroga Mayor

2021 ◽  
Vol 7 (3) ◽  
pp. 7
Author(s):  
Thomas J An ◽  
T. Gregory Walker

Systemic arterial to pulmonary vessel fistulas may develop in the setting of pleural inflammation and/or injury. Bronchial arteries are the most commonly involved vessels, with recruitment often occurring in chronic diseases such as tuberculosis and cystic fibrosis. Rarely, transpleural systemic arteries that directly communicate with the pulmonary vasculature may develop in the presence of pleural injury or chronic inflammation. The clinical presentation and management of three cases of transpleural systemic artery to pulmonary vessel fistulas are detailed. Given the atypical imaging appearance of these lesions, there is risk of misdiagnosis of these entities as a pulmonary arteriovenous malformation. Understanding the pathophysiology, complex anatomy, and treatment for these rare vascular malformations is crucial prior to angiographic intervention in order to improve outcomes, avoid misdiagnosis, and prevent inappropriate intervention.


2010 ◽  
Vol 48 (5) ◽  
pp. 286-291 ◽  
Author(s):  
M. Edward Wilson ◽  
Albrecht Hennig ◽  
Rupal H. Trivedi ◽  
Benjamin J. Thomas ◽  
Sanjay Kumar Singh

2018 ◽  
Vol 103 (10) ◽  
pp. 3620-3629 ◽  
Author(s):  
Masao Takeda ◽  
Koichi Yamamoto ◽  
Hiroshi Akasaka ◽  
Hiromi Rakugi ◽  
Mitsuhide Naruse ◽  
...  

1981 ◽  
Vol 31 (4) ◽  
pp. 360-363 ◽  
Author(s):  
Ray C.J. Chiu ◽  
Milton J. Herba ◽  
Juan Viloria ◽  
David S. Mulder

CHEST Journal ◽  
1972 ◽  
Vol 62 (1) ◽  
pp. 19-23 ◽  
Author(s):  
Bruce H. Brundage ◽  
Alphonse C. Gomez ◽  
Melvin D. Cheitlin ◽  
John T. Gmelich

2021 ◽  
Author(s):  
Shen Zhang ◽  
Jun Qian

Abstract The systemic artery to pulmonary vessel fistula(SAPVF) is an uncommon vascular abnormal communication between systemic arteries (except bronchial arteries) and the lung parenchyma[1]. It can be divided into congenital and acquired causes. Congenital SAPVF is often accompanied by cardiac or pulmonary artery hypoplasia, and acquired are usually caused by pleural adhesions after pleurisy, empyema, trauma, or surgery[2].We report a case of transcatheter arterial embolization for the treatment of congenital right inferior phrenic artery to pulmonary artery fistula.


2003 ◽  
Vol 76 (6) ◽  
pp. 1873-1877 ◽  
Author(s):  
Gregory Riehl ◽  
Philippe Chaffanjon ◽  
Gil Frey ◽  
Carmine Sessa ◽  
Pierre-Yves Brichon

2001 ◽  
Vol 120 (5) ◽  
pp. A234-A234
Author(s):  
R HILSDEN ◽  
M VERHOEF ◽  
A BEST ◽  
R ENNS

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