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[阴道闭锁病例的麦金杜手术。关于该主题的思考]

[McIndoe operation in a case of vaginal agenesis. Considerations on the subject].

作者信息

Sereno J A

机构信息

Hospital General Dr. Miguel Silva, S.S.A. Morelia, Mich.

出版信息

Ginecol Obstet Mex. 1993 Jul;61:190-4.

PMID:8349133
Abstract

Congenital absence of the vagina depends on partial or complete failure of Müllerian duct development. The ovaries develop normally and the fimbrial ends of the tubes are vestigial but there is no uterus, cervix or vagina. The urinary and genital systems and some skeletal portions developing from Müllerian ducts are so closely linked embryologically that congenital abnormality of kidney and bones is said to accompany genital defects in approximately 20% of cases. Several surgical techniques have been proposed but the gynecologist can have sufficient experience to choose the most suitable treatment according to the pecularities of each case. McIndoe Operation offers the best possible result opening a space between the ureta and the rectum and placing within in a large penile shaped mold draped with a split skin graft. This operation can result in a vagina that looks and feels absolutely normal but the most discouraging however is the time required for the completion of the whole treatment. There are several photos illustrating the procedure.

摘要

先天性阴道缺失取决于苗勒管发育部分或完全失败。卵巢发育正常,输卵管伞端发育不全,但没有子宫、宫颈或阴道。从苗勒管发育而来的泌尿系统、生殖系统及一些骨骼部分在胚胎学上联系紧密,以至于约20%的病例中,生殖器缺陷伴有肾脏和骨骼的先天性异常。已经提出了几种手术技术,但妇科医生要有足够经验,根据每个病例的特点选择最合适的治疗方法。麦金杜手术能取得最好的效果,即在尿道和直肠之间开辟一个空间,并在其中放置一个覆盖有裂层皮片的大型阴茎状模具。该手术可形成外观和感觉完全正常的阴道,但最令人沮丧的是整个治疗所需的时间。有几张图片展示了该手术过程。

相似文献

1
[McIndoe operation in a case of vaginal agenesis. Considerations on the subject].[阴道闭锁病例的麦金杜手术。关于该主题的思考]
Ginecol Obstet Mex. 1993 Jul;61:190-4.
2
Müllerian anomalies "without a classification": from the didelphys-unicollis uterus to the bicervical uterus with or without septate vagina.“未分类”的苗勒管异常:从双子宫单宫颈到有或无纵隔阴道的双宫颈子宫。
Fertil Steril. 2009 Jun;91(6):2369-75. doi: 10.1016/j.fertnstert.2008.01.079. Epub 2008 Mar 25.
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Uterine didelphys with duplicated upper vagina and bilateral lower vaginal agenesis: a novel Müllerian anomaly with options for surgical management.双子宫伴双重复上阴道及双侧下阴道闭锁:一种新型苗勒管异常及其手术治疗方案
Fertil Steril. 2008 Mar;89(3):693-8. doi: 10.1016/j.fertnstert.2007.03.062. Epub 2007 Aug 2.
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Double vagina and cervix communicating bilaterally with a single uterine cavity: report of a case with an unusual congenital uterine malformation.双阴道、双宫颈且双侧与单一子宫腔相通:一例罕见先天性子宫畸形病例报告
J Reprod Med. 2007 Mar;52(3):238-40.
5
Müllerian anomalies.苗勒管异常
Semin Reprod Med. 2003 Nov;21(4):375-88. doi: 10.1055/s-2004-815593.
6
Mayer-Rokitansky-Küster-Hauser syndrome of Müllerian agenesis [corrected].苗勒管发育不全的梅耶-罗基坦斯基-库斯特-豪泽综合征[校正后]
Saudi Med J. 2003 May;24(5):532-4.
7
Treatment of patients with a congenital transversal vaginal septum or a partial aplasia of the vagina. The vaginal pull-through versus the push-through technique.先天性横向阴道隔或部分阴道发育不全患者的治疗。阴道拖出术与推进术。
J Pediatr Adolesc Gynecol. 2009 Jun;22(3):157-61. doi: 10.1016/j.jpag.2008.02.008.
8
A normal uterus communicating with a double cervix and the vagina: a müllerian anomaly without any present classification.一个正常子宫与双宫颈及阴道相通:一种未被现有任何分类涵盖的苗勒管异常。
Fertil Steril. 2009 Mar;91(3):935.e1-3. doi: 10.1016/j.fertnstert.2008.09.042. Epub 2008 Nov 11.
9
Congenital malformations of uterus and vagina.子宫和阴道先天性畸形。
Radiologe. 1994 Jul;34(7):397-404.
10
Management of vaginal agenesis.阴道发育不全的管理
Ann Chir Gynaecol. 1980;69(1):37-41.