Literature DB >> 21831509

The female gubernaculum: role in the embryology and development of the genital tract and in the possible genesis of malformations.

Pedro Acién1, Francisco Sánchez del Campo, María-José Mayol, Maribel Acién.   

Abstract

The female gubernaculum is an embryonic structure that gives rise to the uterine round ligament and seems to be important in Müllerian development. In the absence of androgens and anti-Müllerian hormone, the paramesonephric or Müllerian ducts complete their invagination and development, interfering with the connection of the tissue column that begins at the inguinal cone (the gubernaculum) and targets the mesonephric duct and caudal ligament of the gonad. The gubernaculum then grows over the Müllerian ducts, incorporating its muscular fibres. Outside and above this point, the Müllerian ducts give rise to the Fallopian tubes, whereas medially to the point of insertion of the gubernaculum, the Müllerian ducts develop into the normal uterus, the adequate formation of which is also induced by the mesonephric ducts. Diverse human anatomical and physiological characteristics such as the simplex uterus, as well as pathological conditions and certain female genital malformations, could be related to gubernaculum dysfunction. The main conclusions in this article are: (1) The female gubernaculum is the origin of the uterine round ligament but probably not of the uteroovarian ligament. Gubernacula are composed of muscular fibres that probably derive from the abdominal wall and that, when fixed and fused with the Müllerian ducts, allow or induce, together with the mesonephric ducts, the adequate development and formation of the uterus. (2) The female gubernaculum seems to be responsible for many of the specific human characteristics of Müllerian development, including the uterus simplex, the anteflexion and low intra-abdominal position of the uterus, and the disposition of uterine muscular fibres. (3) The female gubernaculum seems to be related to pathologies arising from the round ligaments and inguinal hernia. Likewise, certain uterine malformations (e.g., didelphys uterus, Rokitansky syndrome) and accessory and cavitated uterine masses might be related to gubernaculum dysfunction.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

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Year:  2011        PMID: 21831509     DOI: 10.1016/j.ejogrb.2011.07.040

Source DB:  PubMed          Journal:  Eur J Obstet Gynecol Reprod Biol        ISSN: 0301-2115            Impact factor:   2.435


  16 in total

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2.  Accessory cavitated uterine mass: MRI features and surgical correlations of a rare but under-recognised entity.

Authors:  N Peyron; E Jacquemier; M Charlot; M Devouassoux; D Raudrant; F Golfier; P Rousset
Journal:  Eur Radiol       Date:  2018-08-29       Impact factor: 5.315

3.  Juvenile Cystic Adenomyoma Mimicking a Uterine Anomaly: a Report of Two Cases.

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Journal:  Eurasian J Med       Date:  2017-02

4.  Close relationship between the short round ligament and the ovarian prolapsed inguinal hernia in female infants.

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5.  Comparative histology of mouse, rat, and human pelvic ligaments.

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Journal:  Int Urogynecol J       Date:  2016-04-18       Impact factor: 2.894

6.  MRI evaluation of pelvis in Mayer-Rokitansky-Kuster-Hauser syndrome: interobserver agreement for surgically relevant structures.

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7.  Twin pregnancy in an accessory cavitated non-communicating uterus.

Authors:  Harith M Alkhateeb; Enas M Yaseen
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Review 8.  The comprehensiveness of the ESHRE/ESGE classification of female genital tract congenital anomalies: a systematic review of cases not classified by the AFS system.

Authors:  A Di Spiezio Sardo; R Campo; S Gordts; M Spinelli; C Cosimato; V Tanos; S Brucker; T C Li; M Gergolet; C De Angelis; L Gianaroli; G Grimbizis
Journal:  Hum Reprod       Date:  2015-03-18       Impact factor: 6.918

9.  Challenging Case of Postmenopausal Bleeding and Complete Urogenital Duplication.

Authors:  Olga Grechukhina; Diana P English; Devin Miller; Elena Ratner
Journal:  Am J Case Rep       Date:  2016-05-16

10.  Juvenile cystic adenomyoma, a rare diagnostic challenge: Case Reports and literature review.

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Journal:  F S Rep       Date:  2021-02-10
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