scholarly journals PULMONARY ARTERY ANEURYSM- IDIOPATHIC

2021 ◽  
Vol 54 (2) ◽  
pp. 203-204
Author(s):  
Imran Hameed

SUMMARY A 28-years old female presented with complaints of palpitations and mild retrosternal chest pain. CXR showed a prominent Pulmonary artery. A TTE study revealed a huge main pulmonary artery whereas the branches were of normal size. CT angio revealed aneurysmal main Pulmonary artery and normal sized branches. No concomitant etiology was noted, hence labelled as “idiopathic pulmonary artery aneurysm”. CASE DESCRIPTION A 28-year-old female presented with retrosternal chest pain and palpitations for the last six months. Multiple systolic clicks and murmur III/VI heard in the pulmonary area. ECG was unremarkable. Chest X-Ray showed no cardiomegaly and a prominent pulmonary artery. Transthoracic echocardiography showed aneurysmally dilated main pulmonary artery (size: 5.7cm). Pulmonary valve was thickened with mild regurgitation. CT angiogram demonstrated dilated main pulmonary artery (axial dimension: 5.8cm) with normal-sized branches (Figure1). Immunological workup was negative. She was advised surgical intervention which she agreed to pursue soon at a tertiary care hospital near her hometown. LEARNING POINTS Pulmonary artery aneurysm has an incidence of 1 in 14,000, (based on 109,571 autopsies).1 The maximum normal diameter of MPA is 29mm in males and 27 mm in females. For interlobar branches the maximum size it 17 mm.2 If the size exceeds 4 cm it is “aneurysmal” which may be true of false. PAA could be congenital due to Eisenmenger’ syndrome, Pulmonary valve stenosis and absent pulmonary valve syndrome. Connective tissue disorders (Marfan’s syndrome, alpha-1 antitrypsin deficiency and Ehlers-Danlos syndrome) and autoimmune disorders (Behcet’s disease and Hughes-Stovin syndrome).3 Acquired causes include PAH, auto-immune disease (vasculitis), trauma infections, malignancy and idiopathic. For intervention no consensus of opinion is available. However expert opinion recommends it when the patient becomes symptomatic or pulmonary artery diameter exceeds 5 cm to 6 cm. QUESTIONS WITH ANSWERS Question 1: Is there any difference in the measurement of PA size by echocardiography and CT? Question 2: What is the usual site of dissection in PAA? Question 3: In Pulmonary arterial tree what is the most frequent site of aneurysm? Question 4: Some cases of pulmonary artery aneurysms can be managed medically- Y/N? Question 5: The technique of choice for diagnosing PA aneurysm is pulmonary angiography or CT angiogram? Answers Question 1: Yes Question 2: Main PA Question 3: Right lobar artery Question 4: Yes Question 5: CT angiogram References Deterling RA Jr and Clagett OT. Aneurysm of the pulmonary artery; review of the literature and report of a case. Am Heart J. 1947;34:471-99. Truong QA, Massaro JM, Rogers IS, Mahabadi AA, Kriegel MF, Fox CS. Reference values for normal pulmonary artery dimensions by noncontrast cardiac computed tomography: The Framingham Heart Study. Circ Cardiovasc Imaging 2012;5:147-54. Agarwal S, Chowdhury UK, Saxena A, Ray R, Sharma S, Airan B. Isolated idiopathic pulmonary artery aneurysm. Asian Cardiovasc Thorac Ann. 2002;10(2):167-9.

2002 ◽  
Vol 10 (2) ◽  
pp. 167-169 ◽  
Author(s):  
Saket Agarwal ◽  
Ujjwal Kumar Chowdhury ◽  
Anita Saxena ◽  
Ruma Ray ◽  
Sanjeev Sharma ◽  
...  

Aneurysm formation of the main pulmonary artery is rare. Its natural history is not well understood and there are no clear guidelines on optimal treatment. A 20-year-old woman with a huge saccular aneurysm of the main pulmonary artery, underwent repair with a pericardial patch and concomitant reconstruction of the pulmonary valve. The patient was doing well on follow-up at 6 months; echocardiography revealed a good repair with mild to moderate pulmonary regurgitation.


1989 ◽  
Vol 19 (2) ◽  
pp. 343
Author(s):  
Hong Lyeol Lee ◽  
Myong Ki Hong ◽  
Kyung Kwon Paik ◽  
Seung Jae Tahk ◽  
Woong Ku Lee ◽  
...  

2019 ◽  
Vol 36 (11) ◽  
pp. 2094-2098
Author(s):  
Kianoush Ansari‐Gilani ◽  
Brian D. Hoit ◽  
Robert C. Gilkeson

2007 ◽  
Vol 70 (10) ◽  
pp. 453-455 ◽  
Author(s):  
Hsin-Hung Shih ◽  
Pei-Leun Kang ◽  
Chun-Yao Lin ◽  
Yu-Hsin Lin

2015 ◽  
Vol 31 (1) ◽  
pp. 31-33
Author(s):  
Ramesh Chandra Mishra ◽  
Ramachandra Chandra Barik ◽  
Naresh Kumar Kalludi ◽  
Amaresh Rao Malempati

2020 ◽  
Vol 68 (8) ◽  
pp. 855-857 ◽  
Author(s):  
Yosuke Takahashi ◽  
Toshihiko Shibata ◽  
Masanori Sakaguchi ◽  
Hiromichi Fujii ◽  
Akimasa Morisaki ◽  
...  

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.


2019 ◽  
Vol 107 (6) ◽  
pp. e385-e387
Author(s):  
Sedigheh Saedi ◽  
Kiara Rezaei-Kalantari ◽  
Mozhgan Parsaee ◽  
Mohaddeseh Behjati ◽  
Saeid Hosseini

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