法洛五联症1例报告。

IF 1.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Journal of International Medical Research Pub Date : 2025-04-01 Epub Date: 2025-04-28 DOI:10.1177/03000605251334463
Zhixiong Zhong, Ting Wen
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引用次数: 0

摘要

我们报告的情况下,45岁的妇女与法洛五联症,一个严重的和复杂的紫绀型先天性心脏病。法洛五联症的先天性异常包括室间隔缺损、右心室肥厚、鞍主动脉、肺动脉口狭窄、房间隔缺损、卵圆孔未闭。法洛氏五联症比法洛氏三联症和法洛氏四联症少见,可影响儿童的身体发育。大约95%的法洛五征患者在40岁前死亡,建议早期进行根治性手术。然而,本病例的患者并未接受手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pentalogy of Fallot: A case report.

We report the case of a 45-year-old woman with pentalogy of Fallot, a severe and complicated cyanotic congenital heart disease. Congenital anomalies of pentalogy of Fallot include ventricular septal defect, right ventricular hypertrophy, saddle aorta, pulmonary ostium stenosis, atrial septal defect, and patent foramen ovale. Pentalogy of Fallot is less common than triplet and tetralogy of Fallot and can affect children's physical development. Approximately 95% of patients with pentalogy of Fallot die before the age of 40 years, and early surgical radical surgery is recommended. However, the patient in the current case did not undergo surgery.

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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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