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先天性静脉淋巴管畸形作为青春期前阴道出血的罕见原因

Congenital Venous Lymphatic Malformation as an Unusual Source of Premenarchal Vaginal Bleeding.

作者信息

Homa Lori D, Smorgick-Rosenbaum Noam, Smith Yolanda R, Gemmete Joseph J, Quint Elisabeth H

机构信息

Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, Michigan.

Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, Michigan.

出版信息

J Pediatr Adolesc Gynecol. 2017 Jun;30(3):367-369. doi: 10.1016/j.jpag.2016.02.004. Epub 2016 Feb 13.

Abstract

BACKGROUND

Premenarchal vaginal bleeding can present a diagnostic challenge and has not been previously reported in association with congenital venous lymphatic malformation.

CASE

A 3-year-old girl presented with intermittent vaginal bleeding since birth. Evaluation showed premenarchal estradiol and gonadotropin hormones, a normal pelvic ultrasound and normal colonoscopy. Examination under anesthesia and vaginoscopy showed a congested appearance of the hymen and vaginal petechiae. Sudden development of a vulvar cyst led to a pelvic magnetic resonance imaging scan, which revealed a venous malformation of the pelvis and vulvar lymphatic cyst. Vaginal bleeding stopped for approximately 6 months after sclerotherapy with doxycycline and ethanol, however recurred and required repeat sclerotherapy.

SUMMARY AND CONCLUSION

Congenital venous lymphatic malformations can rarely be associated with premenarchal vaginal bleeding and should be considered when all more common etiologies have been ruled out. Diagnosis is made using magnetic resonance imaging, and treatment might include doxycycline and ethanol sclerotherapy.

摘要

背景

青春期前阴道出血可能带来诊断挑战,且此前未见与先天性静脉淋巴管畸形相关的报道。

病例

一名3岁女孩自出生起出现间歇性阴道出血。评估显示青春期前雌二醇和促性腺激素水平正常,盆腔超声及结肠镜检查正常。麻醉下检查及阴道镜检查显示处女膜充血及阴道瘀点。外阴囊肿突然出现,遂行盆腔磁共振成像扫描,结果显示盆腔静脉畸形及外阴淋巴管囊肿。用强力霉素和乙醇进行硬化治疗后,阴道出血停止约6个月,但复发,需再次进行硬化治疗。

总结与结论

先天性静脉淋巴管畸形很少与青春期前阴道出血相关,在排除所有更常见病因后应予以考虑。通过磁共振成像进行诊断,治疗可能包括强力霉素和乙醇硬化治疗。

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