scholarly journals Huge Pulmonary Artery Aneurysm

2009 ◽  
Vol 16 (3) ◽  
pp. 93-95 ◽  
Author(s):  
Aiman M Hammad ◽  
Sultan M Al-Qahtani ◽  
Mohammed A Al-Zahrani

Pulmonary artery aneurysms (PAAs) are uncommon entities. PAAs are caused mostly by trauma (often iatrogenic), infections and Behcet’s disease (BD). Less common causes are pulmonary hypertension, congenital heart disease and neoplasm. BD is a multisystem disorder presenting with recurrent oral and genital ulcerations, as well as ocular involvement, and PAA is one of its rare complications. A case of huge PAA, in which the usual criteria for the clinical diagnosis of BD were present, is described. Transcatheter embolization resulted in clinical improvement.

2005 ◽  
Vol 29 (1) ◽  
pp. 151-154 ◽  
Author(s):  
Barbaros E. Cil ◽  
Baris Turkbey ◽  
Murat Canyiğit ◽  
Ozlem O. Kumbasar ◽  
Gokhan Celik ◽  
...  

2019 ◽  
Vol 12 (6) ◽  
pp. e230477 ◽  
Author(s):  
Kelly Alice Drivdahl Dougherty ◽  
Mahmoud Elkaissi ◽  
Hani Sabbour ◽  
Samar Farha

2021 ◽  
pp. 1-6
Author(s):  
Ergin Arslanoglu ◽  
Kenan Abdurrahman Kara ◽  
Fatih Yigit ◽  
Cüneyt Arkan ◽  
Esra Ozcan ◽  
...  

Abstract Pulmonary artery aneurysms are rare. They are characterised by an aneurysmatic dilatation of the pulmonary vascular bed, including the main pulmonary artery or the accompanying pulmonary artery branches. Increases in pulmonary flow and pulmonary artery pressure increase the risk of rupture: when these conditions are detected, surgical intervention is necessary. This study is a retrospective analysis of 33 patients treated in our paediatric cardiac surgery clinic from 2012 to 2020. Aneurysms and pseudoaneurysms in patients who were patched for right ventricular outflow tract reconstruction and corrected with a conduit were excluded from the study. Seventeen (51.5%) of the patients included in the study were female and 16 (48.5%) were male. The patients were aged between 23 and 61 years (mean 30.66 ± 12.72 years). Graft interpositions were performed in 10 patients (30.3%) and pulmonary artery plications were performed in 23 patients (69.7%) to repair aneurysms. There was no significant difference in mortality between the two groups (p > 0.05). Pulmonary artery aneurysm interventions are safe, life-saving treatments that prevent fatal complications such as ruptures, but at present there is no clear guidance regarding surgical timing or treatment strategies. Pulmonary artery interventions should be performed in symptomatic patients with dilations ≥5 cm or asymptomatic patients with dilations ≥8 cm; pulmonary artery pressure, right ventricular systolic pressure, and pulmonary artery aneurysm diameter must be considered when planning surgeries, their timing, and making decisions regarding indications. Experienced surgical teams can achieve satisfactory results using one of the following surgical techniques: reduction pulmonary arterioplasty, plication, or graft replacement.


2018 ◽  
Vol 270 ◽  
pp. 120-125 ◽  
Author(s):  
Pastora Gallego ◽  
María José Rodríguez-Puras ◽  
Pilar Serrano Gotarredona ◽  
Israel Valverde ◽  
Begoña Manso ◽  
...  

2018 ◽  
Vol 39 (suppl_1) ◽  
Author(s):  
P Gallego Garcia De Vinuesa ◽  
M J Rodriguez-Puras ◽  
P Serrano ◽  
I Valverde ◽  
B Manso ◽  
...  

Author(s):  
Madhusudana Narayana ◽  
Nagesh Basavaraj ◽  
Smitha Nagaraju ◽  
Jagmohan Sugnyanasagar Venkataramanappa

Abstract We report a rare case of solitary peripheral pulmonary artery aneurysm in a patient who was evaluated for haemoptysis. Incidentally, his total antibodies were positive for Coronavirus 2019 infection. Patient underwent right lower lobectomy uneventfully. Peripheral pulmonary artery aneurysms arising from segmental or intrapulmonary branches are extremely rare. Untreated, the majority end fatally due to sudden rupture and exsanguination. The purpose of this article is to report our rare case and review the pertinent literature.


2021 ◽  
pp. 021849232199849
Author(s):  
Richard Saldanha ◽  
Ravi Ghatanatti ◽  
Mohan D Gan ◽  
Kiran Kurkure ◽  
Gautam Suresh ◽  
...  

Mycotic pulmonary artery aneurysms requiring pneumonectomy are extremely rare. We present a severely breathless immunocompromised diabetic middle-aged female patient. CT pulmonary angiogram revealed a giant pulmonary artery aneurysm with impending rupture in the right lung. We did an emergency right pneumonectomy under cardiopulmonary bypass support. Histopathology report of the lung specimen confirmed mucormycosis. She received amphotericin B after the procedure. The patient had a prolonged postoperative hospital stay and succumbed to sepsis. Mycotic pulmonary artery aneurysm portends very high morbidity and mortality in immunocompromised patients.


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