A rare case of scimitar syndrome with pulmonary arterial hypertension in an adult female

Abstract Scimitar syndrome is a rare congenital anomaly characterized by partial or total anomalous pulmonary venous drainage of the right lung to the inferior vena cava. We report a case of a 67‐year‐old female who presented with cough and dyspnea and was diagnosed with scimitar syndrome and pulmon...

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Main Authors: Yang Liu, Weiliang Ruan, Ziye Li, Hua Wang, Shenghai Chen, Yuhong Ding, Jianfeng Jin
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:Pulmonary Circulation
Subjects:
Online Access:https://doi.org/10.1002/pul2.12332
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author Yang Liu
Weiliang Ruan
Ziye Li
Hua Wang
Shenghai Chen
Yuhong Ding
Jianfeng Jin
author_facet Yang Liu
Weiliang Ruan
Ziye Li
Hua Wang
Shenghai Chen
Yuhong Ding
Jianfeng Jin
author_sort Yang Liu
collection DOAJ
description Abstract Scimitar syndrome is a rare congenital anomaly characterized by partial or total anomalous pulmonary venous drainage of the right lung to the inferior vena cava. We report a case of a 67‐year‐old female who presented with cough and dyspnea and was diagnosed with scimitar syndrome and pulmonary arterial hypertension based on comprehensive imaging and hemodynamic evaluation. This case highlights the importance of considering scimitar syndrome as a cause of pulmonary hypertension even in adult patients.
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spelling doaj.art-d922a3b17a2b4fe59911a9ac5e1a28202024-03-28T19:28:30ZengWileyPulmonary Circulation2045-89402024-01-01141n/an/a10.1002/pul2.12332A rare case of scimitar syndrome with pulmonary arterial hypertension in an adult femaleYang Liu0Weiliang Ruan1Ziye Li2Hua Wang3Shenghai Chen4Yuhong Ding5Jianfeng Jin6Respiratory Department Shaoxing City Keqiao District Hospital of Traditional Chinese Medicine Shaoxing ChinaRespiratory Department Shaoxing City Keqiao District Hospital of Traditional Chinese Medicine Shaoxing ChinaRespiratory Department Shaoxing City Keqiao District Hospital of Traditional Chinese Medicine Shaoxing ChinaSpecial Inspection Department Shaoxing City Keqiao District Hospital of traditional Chinese Medicine Shaoxing ChinaRespiratory Department Shaoxing City Keqiao District Hospital of Traditional Chinese Medicine Shaoxing ChinaRespiratory Department Shaoxing City Keqiao District Hospital of Traditional Chinese Medicine Shaoxing ChinaRespiratory Department Shaoxing City Keqiao District Hospital of Traditional Chinese Medicine Shaoxing ChinaAbstract Scimitar syndrome is a rare congenital anomaly characterized by partial or total anomalous pulmonary venous drainage of the right lung to the inferior vena cava. We report a case of a 67‐year‐old female who presented with cough and dyspnea and was diagnosed with scimitar syndrome and pulmonary arterial hypertension based on comprehensive imaging and hemodynamic evaluation. This case highlights the importance of considering scimitar syndrome as a cause of pulmonary hypertension even in adult patients.https://doi.org/10.1002/pul2.12332computed tomography angiographypulmonary arterial hypertensionscimitar syndrome
spellingShingle Yang Liu
Weiliang Ruan
Ziye Li
Hua Wang
Shenghai Chen
Yuhong Ding
Jianfeng Jin
A rare case of scimitar syndrome with pulmonary arterial hypertension in an adult female
Pulmonary Circulation
computed tomography angiography
pulmonary arterial hypertension
scimitar syndrome
title A rare case of scimitar syndrome with pulmonary arterial hypertension in an adult female
title_full A rare case of scimitar syndrome with pulmonary arterial hypertension in an adult female
title_fullStr A rare case of scimitar syndrome with pulmonary arterial hypertension in an adult female
title_full_unstemmed A rare case of scimitar syndrome with pulmonary arterial hypertension in an adult female
title_short A rare case of scimitar syndrome with pulmonary arterial hypertension in an adult female
title_sort rare case of scimitar syndrome with pulmonary arterial hypertension in an adult female
topic computed tomography angiography
pulmonary arterial hypertension
scimitar syndrome
url https://doi.org/10.1002/pul2.12332
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