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Idiopathic Asymptomatic Aneurysms of Pulmonary Artery and Ascending Aort: A Case Report

Received: 26 January 2017    Accepted: 4 March 2017    Published: 18 December 2017
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Abstract

The dilatation of pulmonary artery is a rare condition and called as pulmonary artery aneurysm. Aneurysm of both the pulmonary trunk and the ascending aorta is even rarer. Symptoms are due to aneurysm compression in adjacent anatomical structures. The main indicator of treatment is the pulmonary artery pressure. The prognosis and treatment of pulmonary artery aneurysm is unclear. Herein we present a case of a main pulmonary artery and ascending aortic aneurysms without underlying pathology. Because our case was asymptomatic, without a initiative cardiac lesion and/or pulmonary hypertension; we decided to follow-up him without operation and he was stable at 24-month follow-up.

Published in International Journal of Cardiovascular and Thoracic Surgery (Volume 3, Issue 6)
DOI 10.11648/j.ijcts.20170306.13
Page(s) 75-77
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Ascending Aortic Aneurysm, Idiopathic, Pulmonary Artery Aneurysm

References
[1] Ercan S, Dogan A, Altunbas G, Davutoglu V. Giant pulmonary artery aneurysm: 12 years of follow-up. case report and review of the literature. Thorac Cardiovasc Surg. 2014; 62 (5): 450-2.
[2] Fraser RS, Müller NL, Colman N, Paré PD. Pulmonary Hypertension and Edema. In: Fraser RS, Müller NL, Colman N, Paré PD, eds. Diagnosis of Diseases of the Chest. Philadelphia, PA: Saunders, 1999: 1935–1937.
[3] Betkier-Lipinska K, Suwalski G, Czarkowski S, Hendzel P, Cwetsch A. Pulmonary artery aneurysm in an adult patient with idiopathic dilatation of the pulmonary artery. Kardiochir Torakochirurgia Pol. 2015; 12 (4): 341-4.
[4] Kreibich M, Siepe M, Kroll J, Höhn R, Grohmann J, Beyersdor F. Aneurysms of the Pulmonary Artery Circulation. 2015; 131: 310-316.
[5] Kotwica T, Szumarska J, Staniszewska-Marszalek E, et al: Idiopathic pulmonary artery aneurysm. Echocardiography 2009; 26: 593–595.
[6] Arslan Ş, Kalkan ME, Gündoğdu F, Kantarcı M. Gögüs ağrısı ile başvuran bir olguda idiyopatik pulmoner arter anevrizması. Arch Turk Soc Cardiol 2009; 37: 253-5.
[7] Shih SY, Tsai IC, Chang YT, Tsan YT, Hu SY. Fatal haemoptysis caused by a ruptured Rasmussens’s aneurysm. Thorax 2011; 66: 553-4.
[8] Deb SJ, Zehr KJ, Shields RC. Idiopathic pulmonary artery aneurysm. Ann Thorac Surg 2005; 80: 1500-1502.
[9] Van Rens MT, Westermann CJ, Postmus PE, Schramel FM. Untreated idiopathic aneurysm of the pulmonary artery: long-term follow-up. Respir Med. 2000; 94: 404 – 405.10.
[10] Kuwaki K, Morishita K, Sato H, Urita R and Abe. Surgical repair of the pulmonary trunk aneurysm. Eur J Cardiothorac Surg. 2000 Nov; 18 (5): 535-9.
[11] Seguchi M, Wada H, Sakakura K, Kubo N, Ikeda N, Sugawara Y, et al. Idiopathic pulmonary artery aneurysm. Circulation. 2011; 124 (14): 369-70.
[12] Sughimoto K, Nakano K, Gomi A, Nakatani H, Nakamura Y, Sato A. Pulmonary artery aneurysm with ascending aortic aneurysm concomitant with bilateral bicuspid semilunar valves. Ann Thorac Surg. 2006; 82 (6): 2270-2.
[13] Hartley JPR, Dinnen JS, Seaton A. Pulmonary and systemic aneurysms in a case of widespread arteries. Thorax 1978; 33: 493–9.
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  • APA Style

    Mihriban Yalcin, Gonul Zeren. (2017). Idiopathic Asymptomatic Aneurysms of Pulmonary Artery and Ascending Aort: A Case Report. International Journal of Cardiovascular and Thoracic Surgery, 3(6), 75-77. https://doi.org/10.11648/j.ijcts.20170306.13

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    ACS Style

    Mihriban Yalcin; Gonul Zeren. Idiopathic Asymptomatic Aneurysms of Pulmonary Artery and Ascending Aort: A Case Report. Int. J. Cardiovasc. Thorac. Surg. 2017, 3(6), 75-77. doi: 10.11648/j.ijcts.20170306.13

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    AMA Style

    Mihriban Yalcin, Gonul Zeren. Idiopathic Asymptomatic Aneurysms of Pulmonary Artery and Ascending Aort: A Case Report. Int J Cardiovasc Thorac Surg. 2017;3(6):75-77. doi: 10.11648/j.ijcts.20170306.13

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  • @article{10.11648/j.ijcts.20170306.13,
      author = {Mihriban Yalcin and Gonul Zeren},
      title = {Idiopathic Asymptomatic Aneurysms of Pulmonary Artery and Ascending Aort: A Case Report},
      journal = {International Journal of Cardiovascular and Thoracic Surgery},
      volume = {3},
      number = {6},
      pages = {75-77},
      doi = {10.11648/j.ijcts.20170306.13},
      url = {https://doi.org/10.11648/j.ijcts.20170306.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijcts.20170306.13},
      abstract = {The dilatation of pulmonary artery is a rare condition and called as pulmonary artery aneurysm. Aneurysm of both the pulmonary trunk and the ascending aorta is even rarer. Symptoms are due to aneurysm compression in adjacent anatomical structures. The main indicator of treatment is the pulmonary artery pressure. The prognosis and treatment of pulmonary artery aneurysm is unclear. Herein we present a case of a main pulmonary artery and ascending aortic aneurysms without underlying pathology. Because our case was asymptomatic, without a initiative cardiac lesion and/or pulmonary hypertension; we decided to follow-up him without operation and he was stable at 24-month follow-up.},
     year = {2017}
    }
    

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    AB  - The dilatation of pulmonary artery is a rare condition and called as pulmonary artery aneurysm. Aneurysm of both the pulmonary trunk and the ascending aorta is even rarer. Symptoms are due to aneurysm compression in adjacent anatomical structures. The main indicator of treatment is the pulmonary artery pressure. The prognosis and treatment of pulmonary artery aneurysm is unclear. Herein we present a case of a main pulmonary artery and ascending aortic aneurysms without underlying pathology. Because our case was asymptomatic, without a initiative cardiac lesion and/or pulmonary hypertension; we decided to follow-up him without operation and he was stable at 24-month follow-up.
    VL  - 3
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Author Information
  • Department of Cardiovascular Surgery, Ordu State Hospital, Ordu, Turkey

  • Department of Cardiology, Ordu State Hospital, Ordu, Turkey

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