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Case report shows effective prenatal diagnosis and surgical management of a rare congenital anomaly, implying improved outcomes.
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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Dorsi et al. (2026) studied this question.
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