Annals of medicine and surgery (2012) · 2026
Dextrocardia with situs solitus in a neonate: a rare case report from Syria.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Shams Aldeen Abd Alkarim, Marta Rana, Tannous Ritchelle, Abo Alaika Tark, Alibrahim Mohamad, Sleiay Bilal, Anis Yaman, Sleiay Mouhammed
Аннотация
INTRODUCTION AND IMPORTANCE: Dextrocardia with situs solitus is an exceptionally rare congenital anomaly. Its asymptomatic nature may delay diagnosis, highlighting the need for careful prenatal and postnatal evaluation.
CASE PRESENTATION: A full-term female neonate was found to have isolated dextrocardia with situs solitus following prenatal suspicion. Postnatal chest X-ray and echocardiography confirmed dextroversion with normal cardiac anatomy and function. No associated anomalies were found. The patient remained asymptomatic and was stable at 3-month follow-up.
CLINICAL DISCUSSION: Isolated dextrocardia with situs solitus is rare and often discovered incidentally. Our case illustrates the importance of thorough prenatal imaging and clinical follow-up to detect potential associated anomalies.
CONCLUSION: Even when asymptomatic, dextrocardia requires comprehensive evaluation. This case contributes to the limited literature and emphasizes the value of imaging and vigilance in similar scenarios.
CASE PRESENTATION: A full-term female neonate was found to have isolated dextrocardia with situs solitus following prenatal suspicion. Postnatal chest X-ray and echocardiography confirmed dextroversion with normal cardiac anatomy and function. No associated anomalies were found. The patient remained asymptomatic and was stable at 3-month follow-up.
CLINICAL DISCUSSION: Isolated dextrocardia with situs solitus is rare and often discovered incidentally. Our case illustrates the importance of thorough prenatal imaging and clinical follow-up to detect potential associated anomalies.
CONCLUSION: Even when asymptomatic, dextrocardia requires comprehensive evaluation. This case contributes to the limited literature and emphasizes the value of imaging and vigilance in similar scenarios.