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二维/四维超声中孕期扫描诊断胎儿腋窝部淋巴管瘤:病例报告及文献复习。

Fetal axillary lymphangioma diagnosed on a 2D/4D ultrasound second trimester scan - a case report and short literature review.

机构信息

Department of Obstetrics and Gynecology Clinical Emergency Hospital "Sf. Ap. Andrei" Galati University "Dunarea de Jos", Faculty of Medicine and Pharmacy, Galati, Romania.

University "Dunarea de Jos", Faculty of Medicine and Pharmacy, Galati, Romania.

出版信息

Med Ultrason. 2021 Nov 25;23(4):490-492. doi: 10.11152/mu-2531. Epub 2020 Jun 13.

Abstract

Fetal lymphangioma, also known as cystic hygroma, is a hamartomatous congenital tumor which involves the fetal skin and the subcutaneous tissue. The most common site of appearance is in the neck region. Location of the lesion in the axilla as well as in other anathomical sites is very rare.Prenatal diagnosis can be made on ultrasound examination. Other structural or chromosomal anomalies are frequently associated with this diagnosis. The antepartum management and type of delivery should be set up by a multidisciplinary team.We present a rare case diagnosed with axillary lymphangioma during the second trimester morphological ultrasound 2D/4D scan.

摘要

胎儿淋巴管瘤,亦称囊状水瘤,是一种涉及胎儿皮肤和皮下组织的先天性错构瘤。最常见的发病部位是颈部。腋窝及其他解剖部位的病变极为罕见。产前超声检查可做出诊断。该诊断常伴有其他结构或染色体异常。应通过多学科团队设置产前管理和分娩方式。我们报告了一例罕见病例,该病例在中期形态学二维/四维超声扫描时被诊断为腋窝淋巴管瘤。

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