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心脏脂肪瘤致新生儿低氧血症:强调放射学诊断的病例报告及文献综述

Cardiac lipoma-induced neonatal hypoxemia: a case report underscoring radiological diagnosis and a literature review.

作者信息

Al-Bitar Ahmad, Al Malla Ahmad, Redan Lana, Tellawi Israa, Al Helbawi Hussien, Al-Dairy Alwaleed

机构信息

Faculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.

Department of Radiology, Damascus Hospital, Damascus, Syrian Arab Republic.

出版信息

Radiol Case Rep. 2025 Jul 28;20(10):5196-5204. doi: 10.1016/j.radcr.2025.06.098. eCollection 2025 Oct.

Abstract

Cardiac tumors in neonates are exceedingly rare, with cardiac lipomas representing an exceptionally uncommon subtype associated with high mortality due to hemodynamic compromise. This report presents a 2-day-old Arab male neonate admitted with acute hypoxemia and cardiomegaly. Echocardiography and CT imaging revealed a large hyperechoic, fatty-density mass (3.8 × 3.5 × 3.3 cm) in the left ventricle, suggestive of a cardiac lipoma, but biopsy or surgical intervention could not be performed due to rapid clinical deterioration culminating in fatal cardiopulmonary failure. This case underscores the diagnostic and therapeutic challenges of neonatal cardiac tumors, highlighting the need for clinical suspicion and early prenatal surveillance to avoid their life-threatening mass effects and enable multidisciplinary planning. Future research should prioritize biomarkers, risk-stratification tools, and improved imaging algorithms to facilitate timely diagnosis and intervention in low-resource contexts.

摘要

新生儿心脏肿瘤极为罕见,心脏脂肪瘤是一种极其罕见的亚型,由于血流动力学受损,其死亡率很高。本报告介绍了一名2日龄的阿拉伯男婴,因急性低氧血症和心脏肿大入院。超声心动图和CT成像显示左心室有一个大的高回声、脂肪密度肿块(3.8×3.5×3.3厘米),提示为心脏脂肪瘤,但由于临床迅速恶化最终导致致命的心肺衰竭,无法进行活检或手术干预。该病例强调了新生儿心脏肿瘤的诊断和治疗挑战,突出了临床怀疑和早期产前监测的必要性,以避免其危及生命的占位效应,并实现多学科规划。未来的研究应优先关注生物标志物、风险分层工具和改进的成像算法,以便在资源有限的情况下促进及时诊断和干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c19/12320533/f4702613209b/gr1.jpg

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