Results 31 to 40 of about 1,551 (154)
Porous poly-l-lactide-co-ɛ-caprolactone scaffold: a novel biomaterial for vaginal tissue engineering [PDF]
Royal Society Open Science, 2018 The surgical reconstruction of functional neovagina is challenging and susceptible to complications. Therefore, developing tissue engineering-based treatment methods for vaginal defects is important.
Reetta Sartoneva +9 more
doaj +1 more source
Brazilian Journal of Medical and Biological Research, 1997 We present an ultrastructural study of the utilization of human amniotic membrane in the treatment of congenital absence of the vagina in 10 patients. All patients were surgically treated with application of an amniotic membrane graft using the modified ...
L.F. Bleggi-Torres +2 more
doaj +1 more source
European Journal of Pediatric Surgery Reports, 2021 Anorectal malformation with rectovestibular fistula associated with vaginal agenesis is rare. We report on a child in whom this combination was diagnosed at the age of 1 year. After creation of a divided descending colostomy, we chose to leave the rectum-
Antonio Dessanti +3 more
doaj +1 more source
Sexuelle Zufriedenheit von Frauen mit vaginaler Aplasie nach operativer Neovagina-Bildung [PDF]
, 2008 Obwohl kein sehr seltenes Phänomen, stellt der Befund einer Aplasie von Uterus und Vagina (Mayer-Rokitansky-Küster-Hauser-Syndrom) ein im Allgemeinen wenig bekanntes Thema dar.
Marcollo Pini, A R
core +2 more sources
Journal of Human Reproductive Sciences, 2016 Context: Host of vaginoplasty techniques have been described. None has been successful in developing normal vagina. Laparoscopic peritoneal vaginoplasty (LPV) is performed in Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) culminating in normal vagina ...
Pravin N Mhatre +4 more
doaj +1 more source
McIndoe Vaginoplasty in MRKHS: Case Report and Literature Review. [PDF]
Clin Case RepABSTRACT Mayer–Rokitansky–Küster–Hauser syndrome (MRKHS) is a rare congenital disorder characterized by agenesis of the uterus and upper two‐thirds of the vagina. It affects around 1 in 4000–5000 females and is of two types: type 1, also known as isolated Müllerian aplasia or Rokitansky, which involves only uterovaginal agenesis, and type 2, presents ...
Shah NA +7 more
europepmc +2 more sources
Condylomata acuminata of the neovagina in a HIV-seropositive male-to-female transsexual
, 2004 We present an unusual case of condylomata acuminata arising in the transplanted skin of a neovagina in a male-to-female transsexual. The neovagina had been constructed using a penile and a scrotal skin flap.
DE SETA F. +6 more
core +2 more sources
GMS Interdisciplinary Plastic and Reconstructive Surgery DGPW, 2016 Vaginal agenesis is a congenital anomaly that affects the life of one of each four thousand women around the world. There is a trend that patients request immediate surgical correction, instead of passive vaginal dilatation.
Torres-de la Roche, Luz Angela +6 more
doaj +1 more source
Double Pedicle Artery Rotation Sigmoid Vaginoplasty for Vaginal Aplasia Management [PDF]
Annals of Coloproctology, 2020 Sigmoid vaginoplasty has been popular for neovagina reconstruction in vaginal aplasia. The most common surgical complication was vaginal stenosis caused by inadequate vascularization and tension because of graft length.
Adeodatus Yuda Handaya +8 more
doaj +1 more source
Biomedical Papers, 2021 Mayer-Rokitansky-Küster-Hauser syndrome is a rare female congenital anomaly that presents with an inability to have coital sexual intercourse and absolute uterine factor infertility.
Roman Chmel +4 more
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