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[直肠后囊性错构瘤。1例经阴道切除术的报告及文献复习]

[Retrorectal cystic hamartoma. Report of one case with vaginal resection and review of the literature].

作者信息

Delemer M, Detchev R, Dugue T, Gosset P, Houzé de l'Aulnoit D

机构信息

Service de gynécologie obstétrique, hôpital Saint-Vincent-de-Paul, GHICL, boulevard de Belfort, BP 387, 59020 Lille cedex, France.

出版信息

J Gynecol Obstet Biol Reprod (Paris). 2011 Oct;40(6):569-71. doi: 10.1016/j.jgyn.2010.12.009. Epub 2011 Feb 25.

Abstract

Tailgut cyst is a rare congenital presacral lesion. We report a case of a 24-year-old woman presenting a recurrent retrorectal mass with pain. Surgical resection by vaginal way found retrorectal cystic hamartoma. Differential diagnosis include cystic teratoma, epidermal cyst and rectal duplication cysts. The most important complications are recurrence, infection, perineal fistulas and the possibility of malignant transformation. So the complete surgical excision of these lesion is necessary.

摘要

尾肠囊肿是一种罕见的先天性骶前病变。我们报告一例24岁女性,出现复发性直肠后肿块并伴有疼痛。经阴道手术切除发现直肠后囊性错构瘤。鉴别诊断包括囊性畸胎瘤、表皮样囊肿和直肠重复囊肿。最重要的并发症是复发、感染、会阴瘘以及恶变的可能性。因此,对这些病变进行完整的手术切除是必要的。

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引用本文的文献

1
Tailgut cyst: 2 case reports.尾肠囊肿:2例病例报告。
Clin Case Rep. 2021 Jul 16;9(7):e04490. doi: 10.1002/ccr3.4490. eCollection 2021 Jul.

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