Massive left pulmonary artery aneurysm with a co-existing patent ductus arteriosus in a five-year-old female child: a case report

Authors

  • Javeria Khan National Institute of Cardiovascular Diseases, Karachi, Pakistan https://orcid.org/0000-0002-6629-6241
  • Muhammad Mansoor Khan National Institute of Cardiovascular Diseases, Karachi, Pakistan
  • Zubair Brohi National Institute of Cardiovascular Diseases, Karachi, Pakistan
  • Mahwish Mahboob National Institute of Cardiovascular Diseases, Karachi, Pakistan
  • Sohail Khan Bangash National Institute of Cardiovascular Diseases, Karachi, Pakistan

DOI:

https://doi.org/10.47391/JPMA.9952

Keywords:

pulmonary artery aneurysm (PAA), patent ductus arteriosus (PDA), cardiac aneurysm, left pulmonary artery, saccular aneurysm

Abstract

Pulmonary Artery Aneurysm (PAA), whether congenital or acquired, is a rare diagnostic finding compared to aortic aneurysms. There have been few cases where PAAs were documented as a complication of untreated Patent Ductus Arteriosus (PDA) due to long-standing Pulmonary Arterial Hypertension (PAH). However, it is quite rare for a case of PAA to be reported with co-existing PDA without PAH. This report highlights a case of a five-year-old girl who was presented with palpitations, easy fatigability, fever, cyanosis, and vomiting. A Chest X-ray showed moderate cardiomegaly. A PDA of 6 mm was diagnosed on Transthoracic Echocardiography (TTE) and a large cavity connected with LPA raised suspicion of a possible LPA aneurysm. A Chest CT scan confirmed the diagnosis of a saccular aneurysm, originating from the distal part of the main Left Pulmonary Artery (LPA) just proximal to the point of bifurcation into lobar branches, measuring 7.5 x 6.5 cm.

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Published

2024-02-11

How to Cite

Javeria Khan, Khan, M. M., Zubair Brohi, Mahwish Mahboob, & Sohail Khan Bangash. (2024). Massive left pulmonary artery aneurysm with a co-existing patent ductus arteriosus in a five-year-old female child: a case report. Journal of the Pakistan Medical Association, 74(3), 585–588. https://doi.org/10.47391/JPMA.9952

Issue

Section

CASE REPORT