Prenatal Diagnosis of a Congenital Pseudoaneurysm of the Mitral-Aortic Intervalvular Fibrosa: A Multimodality Imaging Case Report

Abstract Background Congenital pseudoaneurysm of the mitral-aortic intervalvular fibrosa (P-MAIVF) is exceptionally rare, and prenatal diagnosis remains challenging. Case Summary We report a rare case of a congenital P-MAIVF diagnosed prenatally. The fetus was closely monitored throughout pregnancy and after birth. Surgical resection was performed at 12 months because of progressive enlargement and concern for fistula formation. The combination of imaging techniques helped in detecting the complication and guiding management. Postoperative outcome was excellent. Discussion The diagnosis of such a rare congenital anomaly is challenging and improving its recognition is essential. Multimodality imaging may help in diagnosis, clinical decision making and longitudinal follow-up.

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Publication Details

Journal
European Heart Journal - Case Reports
Published
2026-06-16
DOI
https://doi.org/10.1093/ehjcr/ytag461
Primary Topic
Infective Endocarditis Diagnosis and Management
Type
article
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article

Prenatal Diagnosis of a Congenital Pseudoaneurysm of the Mitral-Aortic Intervalvular Fibrosa: A Multimodality Imaging Case Report

Emmanuelle Fournier, Igor Deryabin, Marine Dorsi, E Valdeolmillos et al.
European Heart Journal - Case Reports
Infective Endocarditis Diagnosis and Management
article

Prenatal Diagnosis of a Congenital Pseudoaneurysm of the Mitral-Aortic Intervalvular Fibrosa: A Multimodality Imaging Case Report

Emmanuelle Fournier, Igor Deryabin, Marine Dorsi, E Valdeolmillos, Clement Batteux
article en

Abstract

Abstract Background Congenital pseudoaneurysm of the mitral-aortic intervalvular fibrosa (P-MAIVF) is exceptionally rare, and prenatal diagnosis remains challenging. Case Summary We report a rare case of a congenital P-MAIVF diagnosed prenatally. The fetus was closely monitored throughout pregnancy and after birth. Surgical resection was performed at 12 months because of progressive enlargement and concern for fistula formation. The combination of imaging techniques helped in detecting the complication and guiding management. Postoperative outcome was excellent. Discussion The diagnosis of such a rare congenital anomaly is challenging and improving its recognition is essential. Multimodality imaging may help in diagnosis, clinical decision making and longitudinal follow-up.

European Heart Journal - Case Reports
Hospital for Sick Children (CA), Centre Hospitalier Intercommunal de Poissy (FR), Hôpital Marie Lannelongue (FR)
Peace, Justice and strong institutions
Openalex Percentile: Top 6%
Infective Endocarditis Diagnosis and Management
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