Isolated Idiopathic Pulmonary Artery Aneurysm

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.

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.


2019 ◽  
Vol 30 (1) ◽  
pp. 159-160
Author(s):  
Davide Carino ◽  
Nikita Mehta ◽  
Alejandro Fernández-Cisneros ◽  
Daniel Pereda

Abstract Pulmonary artery aneurysms are rare but are associated with a significant risk of rupture and dissection. Moreover, pulmonary valve regurgitation and/or stenosis often coexist. In this study, we present a case of a pulmonary artery aneurysm with severe pulmonary regurgitation in a patient with pulmonary hypertension treated with aneurysm resection and pulmonary valve repair.


Author(s):  
Veronica Lorenz ◽  
Andrea Gambacciani ◽  
Susanna Guerrini ◽  
Mazzei Francesco Giuseppe ◽  
Montesi Gianfranco ◽  
...  

AbstractThe pulmonary artery aneurysm (PAA) is a rare disease with no well-defined guidelines about the diagnostic criteria and its management. In fact, the indications for surgical treatment and the type of surgical approach are not clear. However, in case of giant PAAs with hypertension and pulmonary valve abnormalities, surgery should be considered as an effective and safe approach to prevent dissections or ruptures. In this report, we describe a successful case of surgical repair, using a Bioconduit with a pericardial patch to recreate the pulmonary artery bifurcation in a 72-year-old male with aneurysm of the pulmonary artery (max diameter: 72 mm), associated with quadricuspid pulmonary valve stenosis and pulmonary hypertension. The procedure was uncomplicated and the follow-up computed tomography scan at 4 months showed correct positioning of the graft with no sign of contrast leakage.


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

2020 ◽  
Vol 30 (6) ◽  
pp. 943-944
Author(s):  
Xiaobing Li ◽  
Xian Fan ◽  
Li Shen ◽  
Rufang Zhang

Abstract Pulmonary artery (PA) aneurysm is a very rare complication of Behcet’s disease. We report on a 14-year-old boy with a giant left distal PA aneurysm caused by Behcet’s disease. A left thoracotomy was first performed to separate the aneurysm, but it was interrupted due to continuous and massive tracheorrhagia. We immediately converted to a median sternotomy and established cardiopulmonary bypass (CPB). The patient’s condition was stable; aneurysmectomy and left-down lobectomy were successfully performed. Results of the 2-year follow-up were favourable. Based on our experience, we recommend selecting CPB when performing surgery on patients with PAA, especially those with Behcet’s disease.


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

2010 ◽  
Vol 90 (6) ◽  
pp. 2049-2051 ◽  
Author(s):  
Nagarajan Muthialu ◽  
Vijayakumar Raju ◽  
Venkatadevanathan Muthubaskaran ◽  
Padmanabhan Chandrasekar ◽  
Srinivasan Muralidharan ◽  
...  

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