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Case Reports in Cardiology
Volume 2014, Article ID 427045, 3 pages
http://dx.doi.org/10.1155/2014/427045
Case Report

Accidental Left Circumflex Artery to Right Lung Fistula in a Suspected Case of Pulmonary Hypertension

1Cardiovascular Research Center, Modarres Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
2Prevention of Metabolic Disorders Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran
3Cardiovascular Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran

Received 17 April 2014; Revised 29 June 2014; Accepted 29 June 2014; Published 17 July 2014

Academic Editor: Ramazan Akdemir

Copyright © 2014 Saeed Alipourparsa et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

A 56-year-old woman was referred to the cardiology department of the Shahid Modarres hospital. The patient had a history of pulmonary thromboembolism 20 years ago which had been managed by the inferior vena cava filter and since then the patient has been on warfarin. Her chief complaint was chronic dyspnea on exertion (NYHA class II) from several years ago. Right and left heart catheterization was performed for evaluation of pulmonary artery pressure. We found rich collateral formations between LCX as well as RCA and right pulmonary artery, primarily assumed as multiple fistulas. Among patients who have chronic thromboembolic pulmonary hypertension, systemic collateral supply to the pulmonary parenchyma has been previously reported to occur from both bronchial and/or nonbronchial systemic circulations. Our patient had neither signs of heart failure nor myocardial ischemia and, thus, was a candidate for conservative management. The adenosine pulmonary reactivity test was not performed because of low pulmonary pressure which had been estimated to be high.