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CASE REPORT article

Front. Pediatr.

Sec. Pediatric Cardiology

Volume 13 - 2025 | doi: 10.3389/fped.2025.1624029

This article is part of the Research TopicPediatric and Perinatal Cardiology; Insights, Advances and UpdatesView all 9 articles

A thrombosis of ductus arteriosus aneurysm involving the left pulmonary artery in a full-term newborn with isolated right ventricular hypoplasia

Provisionally accepted
Stasa  KrasicStasa Krasic1,2Nevena  DjorovicNevena Djorovic2Ivan  DizdarevicIvan Dizdarevic2Vesna  TopicVesna Topic2Nikola  IlicNikola Ilic2Adrijan  SarajlijaAdrijan Sarajlija1,2Dragana  AleksicDragana Aleksic2Vladislav  VukomanovićVladislav Vukomanović1,2*
  • 1Faculty of Medicine, University of Belgrade, Belgrade, Serbia
  • 2Mother and Child Health Institute of Serbia, Belgrade, Serbia

The final, formatted version of the article will be published soon.

Background: Thrombosis of ductus arteriosus aneurysm (DAA) is a well-known complication of DAA that can lead to vascular obstruction or thromboembolic events. Case report: A full-term male newborn presented with isolated right ventricular hypoplasia (IRVH). Follow-up echocardiography at 19 days of life revealed a pedunculated mass, suggesting a thrombus partially obstructing the left pulmonary artery (LPA). The patient remained clinically stable but was admitted to the neonatal intensive care unit for close monitoring. CT and MRI confirmed DAA thrombosis involving LPA. Due to a lack of resolution with conservative treatment, the patient underwent a thrombectomy and resection of the ductus arteriosus (DA). The postoperative course was uneventful, and the follow-up echocardiography showed normalisation of the right ventricular cavity and no residual thrombus. Conclusion: This case highlights the importance of early detection and investigation in neonates with echocardiographic findings of intrauterine ductus arteriosus closure, stenosis, or DA closure in the first 12 hours of life to prevent life-threatening complications.

Keywords: Ductus arteriosus aneurysm, Pulmonary artery thrombus, Isolated right ventricular hypoplasia, neonates, case report

Received: 06 May 2025; Accepted: 11 Sep 2025.

Copyright: © 2025 Krasic, Djorovic, Dizdarevic, Topic, Ilic, Sarajlija, Aleksic and Vukomanović. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Vladislav Vukomanović, vvukomanovicdr@gmail.com

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