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产前诊断的胎儿头皮血管瘤完全消退。

Complete involution of prenatally-diagnosed fetal scalp hemangioma.

作者信息

Jo Eun Ju, Choi Suk-Joo, Oh Soo-young, Park Byung Kwan, Roh Cheong-Rae, Kim Jong-Hwa

机构信息

Department of Obstetrics and Gynecology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

Department of Obstetrics and Gynecology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

出版信息

Taiwan J Obstet Gynecol. 2014 Mar;53(1):86-9. doi: 10.1016/j.tjog.2013.10.038.

Abstract

OBJECTIVE

Scalp hemangioma is a rare benign fetal tumor. Here, we describe the detailed imaging features and natural course of a fetal scalp hemangioma until 1 year of age.

CASE REPORT

We encountered a case of scalp hemangioma at 23 weeks' gestation by prenatal ultrasonography and magnetic resonance imaging. The mass persisted postnatally, but spontaneously regressed after birth.

CONCLUSION

Proper diagnosis with prenatal ultrasonography and magnetic resonance imaging is important when a scalp mass is suspected in utero. Continuation of the pregnancy after appropriate counseling is prudent, considering the favorable prognosis and the rate of spontaneous regression of uncomplicated cases.

摘要

目的

头皮血管瘤是一种罕见的胎儿良性肿瘤。在此,我们描述一例胎儿头皮血管瘤直至1岁时的详细影像学特征及自然病程。

病例报告

我们通过产前超声和磁共振成像在孕23周时发现一例头皮血管瘤。该肿块出生后持续存在,但出生后自行消退。

结论

当子宫内怀疑有头皮肿块时,产前超声和磁共振成像的正确诊断很重要。考虑到预后良好以及单纯病例的自发消退率,在适当咨询后继续妊娠是谨慎的做法。

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