THE MAYER-ROKITANSKY-KUSTER-SYNDROME - AN ANALYSIS OF ITS MORPHOLOGY AND EMBRYOLOGY - PART II - EMBRYOLOGY

Authors
Citation
Ks. Ludwig, THE MAYER-ROKITANSKY-KUSTER-SYNDROME - AN ANALYSIS OF ITS MORPHOLOGY AND EMBRYOLOGY - PART II - EMBRYOLOGY, Archives of gynecology and obstetrics, 262(1-2), 1998, pp. 27-42
Citations number
25
Categorie Soggetti
Obsetric & Gynecology
ISSN journal
09320067
Volume
262
Issue
1-2
Year of publication
1998
Pages
27 - 42
Database
ISI
SICI code
0932-0067(1998)262:1-2<27:TM-AAO>2.0.ZU;2-R
Abstract
The Mullerian duct (MD; ductus paramesonephricus) develops independent of the coelomic epithelium above the mesonephros. This part of the du ct gives rise to the infundibulum with its fimbriated ostium abdominal e. The part of the duct which lies along the mesonephros as far as its caudal pole makes a contribution to the ampulla and less often the is thmus. In the area of the mesonephros the MD fuses with the Wolffian d uct (WD; ductus mesonephricus). The WD gives rise to the ampulla and t he isthmus. Below the caudal pole of the mesonephros, as well as beyon d the attachment point of the inguinal ligament of the mesonephros, th e later round ligament of the uterus, the MD develops as an outgrowth of the WD and no longer as an independent structure. The MRK syndrome is, in its formal genesis, a non-fusion of the MD with the WD. This ex plains the fact that in a das sic case of MRK syndrome, the Fallopian tube with a very small part of the cornu uteri extends only as far as the connection with the round ligament of the uterus. Different possib ilities for the origin of MRK syndrome are discussed. It is suggested that the cause of the development of MRK syndrome could be a deficienc y of gestagen and/or oestrogen receptors. This would also explain the various forms of the rudimentary vagina.