Abstract:The authors reviewed 32 patients who underwent vaginal reconstruction using a modified McIndoe procedure during the past 15 years. This technique consists of the application of split-thickness skin grafts into a new cavity created between the rectum, bladder, and urethra. The grafts are placed previously on a mold of Optosil, which is a silicon-based condensation curing impression material used by dentists. The mold is kept for 3 months 24 hours each day. During the next 3 to 4 weeks it is applied 12 hours per… Show more
“…In most of these studies the focus was on assessing the outcome of neovaginal surgeries (e.g., Rajimwale, Furness, Brant, & Koyle, 2004;Seccia et al, 2002). The fact that both condition groups share a DSD diagnosis that includes infertility but that the following differences also exist makes MRKHS an appropriate comparison group for CAIS studies in general: In CAIS, a defect of the androgen receptor gene leads to infertility and a feminine phenotype despite the presence of inguinal testes and 46,XY karyotype.…”
The perception of gender development of individuals with complete androgen insensitivity syndrome (CAIS) as unambiguously female has recently been challenged in both qualitative data and case reports of male gender identity. The aim of the mixed-method study presented was to examine the self-perception of CAIS individuals regarding different aspects of gender and to identify commonalities and differences in comparison with subfertile and infertile XX-chromosomal women with diagnoses of Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) and polycystic ovary syndrome (PCOS). The study sample comprised 11 participants with CAIS, 49 with MRKHS, and 55 with PCOS. Gender identity was assessed by means of a multidimensional instrument, which showed significant differences between the CAIS group and the XX-chromosomal women. Other-than-female gender roles and neither-female-nor-male sexes/genders were reported only by individuals with CAIS. The percentage with a not exclusively androphile sexual orientation was unexceptionally high in the CAIS group compared to the prevalence in "normative" women and the clinical groups. The findings support the assumption made by Meyer-Bahlburg ( 2010 ) that gender outcome in people with CAIS is more variable than generally stated. Parents and professionals should thus be open to courses of gender development other than typically female in individuals with CAIS.
“…In most of these studies the focus was on assessing the outcome of neovaginal surgeries (e.g., Rajimwale, Furness, Brant, & Koyle, 2004;Seccia et al, 2002). The fact that both condition groups share a DSD diagnosis that includes infertility but that the following differences also exist makes MRKHS an appropriate comparison group for CAIS studies in general: In CAIS, a defect of the androgen receptor gene leads to infertility and a feminine phenotype despite the presence of inguinal testes and 46,XY karyotype.…”
The perception of gender development of individuals with complete androgen insensitivity syndrome (CAIS) as unambiguously female has recently been challenged in both qualitative data and case reports of male gender identity. The aim of the mixed-method study presented was to examine the self-perception of CAIS individuals regarding different aspects of gender and to identify commonalities and differences in comparison with subfertile and infertile XX-chromosomal women with diagnoses of Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) and polycystic ovary syndrome (PCOS). The study sample comprised 11 participants with CAIS, 49 with MRKHS, and 55 with PCOS. Gender identity was assessed by means of a multidimensional instrument, which showed significant differences between the CAIS group and the XX-chromosomal women. Other-than-female gender roles and neither-female-nor-male sexes/genders were reported only by individuals with CAIS. The percentage with a not exclusively androphile sexual orientation was unexceptionally high in the CAIS group compared to the prevalence in "normative" women and the clinical groups. The findings support the assumption made by Meyer-Bahlburg ( 2010 ) that gender outcome in people with CAIS is more variable than generally stated. Parents and professionals should thus be open to courses of gender development other than typically female in individuals with CAIS.
“…This anomaly is associated with a lasting negative psychological impact on women. However, the main problems are the inability to establish a sexual life and reproductive problems, which could wait until beginning sexual activity (38,(109)(110)(111)(112)(113).…”
Section: Correlation With Clinical Presentation and Prognosismentioning
“…Different types of grafts have been used; split thickness skin graft harvested from various sites and rotational flaps (fasciocutaneus and muscolocutaneus). The main disadvantages of this procedure are the visible scar, including keloids and infection [Seccia et al, 2002;Klingele et al, 2003], inadequate lubrication and high rate of graft stenosis necessitating frequent and potentially life long dilation. Long-term sexual function results have not been validated; however, sexual satisfaction rates have been reported to be between 80 and 90% [Mobus et al, 1996;Keser et al, 2005].…”
Patients with disorders of sexual development (DSD) requiring vaginal reconstruction are complex and varied in their presentation. Enlargement procedures for vaginal hypoplasia include self-dilation therapy or surgical vaginoplasty. There are many vaginoplasty techniques described, and each method has different risks and benefits. Reviewing the literature on management options for vaginal hypoplasia, the results show a number of techniques available for the creation of a neovagina. Studies are difficult to compare due to their heterogeneity, and the indications for surgery are not always clear. Psychological support improves outcomes. There is a paucity of evidence to inform management regarding the optimum surgical technique to use, and long-term data on success is lacking, particularly with respect to sexual function. In conclusion, vaginal dilators remain the cornerstone of treatment of women with vaginal hypoplasia and should be used as the first-line technique. Surgical vaginoplasty has a role in complex patients with previous failed dilation and surgical intervention, particularly those cases where there is significant scarring from previous surgery. Regardless of the vaginal reconstruction technique, patients should be managed in a multidisciplinary team where there is adequate emotional and psychological support available.
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