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Journal articles on the topic 'Agenesia vaginal'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Fernández Fernández, Jesús Ángel, and Grisel María Marín Rincón. "Síndrome de Mayer-Rokitansky- Küster-Hauser asociado con malformación anorectal." Revista Repertorio de Medicina y Cirugía 28, no. 3 (2019): 191–95. http://dx.doi.org/10.31260/repertmedcir.v28.n3.2019.962.

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La agenesia vaginal es una entidad poco frecuente que puede presentarse en forma aislada o acompañada de otras anomalías congénitas. El desconocimiento de esta asociación puede retardar su diagnóstico, causar complicaciones indeseadas y comprometer el resultado del tratamiento. Se describen tres casos clínicos con agenesia vaginal y malformación anorrectal, cuyos diagnósticos no fueron realizados en el momento del nacimiento. Aunque la coexistencia de anomalías vaginales y anorectales sean poco frecuentes, los médicos responsables de su tratamiento deben ser conscientes de su existencia y prac

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2

Alcántara Ascón, René, and Víctor Díaz Huamán. "AGENESIA VAGINAL EN EL HOSPITAL ARZOBISPO LOAYZA LIMA-PERU." Revista Peruana de Ginecología y Obstetricia 35, no. 7 (2015): 10–13. http://dx.doi.org/10.31403/rpgo.v35i1030.

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Se estudia 12 pacientes con agenesia vaginal, atendidos entre Abril de 7970 a Marzo de 1988, con el propósito de presentar su incidencia, manejo y complicaciones. Se encontró un caso por cada 3,311 hospitalizaciones. La agenesia vaginal como hallazgo único la tuvieron 4 mujeres, en las otras 8 hubo además útero rudimentario (3 casos), agenesia uterina (2 casos), feminización testicular (1 caso), prosis renal bilateral (1 caso) y bifidez ureteral (1 caso). Las técnicas de vaginasplastía fueron las de Wharton (5 casos) y de Mc Indoe (3 casos). No existió complicaciones en 3 pacientes, mientras q

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3

Aristizábal-Duque, Jorge Enrique, and Joan Camilo Piedrahíta-Mejía. "Seguridad y eficacia de la vaginoplastia de Vecchietti en agenesia vaginal: estudio de cohorte, en Medellín, Colombia, 2007 a 2012." Revista Colombiana de Obstetricia y Ginecología 70, no. 3 (2019): 165–73. http://dx.doi.org/10.18597/rcog.3177.

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Objetivo: describir la técnica de vaginoplastia de Vecchietti (TVV) en pacientes diagnosticadas con agenesia vaginal secundaria y hacer una aproximación a la seguridad y eficacia de esta técnica. Materiales y métodos: cohorte histórica de pacientes con agenesia vaginal secundaria al síndrome de Mayer-Rokitansky-Kuster-Hauser y al síndrome de insensibilidad androgénica, a quienes se les realizó vaginoplastia por técnica de Vecchietti en el Hospital Universitario San Vicente Fundación, institución de referencia, de alta complejidad, en el periodo 2007 a 2012. Se excluyeron quienes tenían una vag

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4

Gutiérrez, Carlos, Jorge Han, and René Alcántara. "ANOMALIAS DEL APARATO GENITAL FEMENINO." Revista Peruana de Ginecología y Obstetricia 32, no. 4 (2015): 14–17. http://dx.doi.org/10.31403/rpgo.v32i602.

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Se realizó un estudio de 58 pacientes con anomalías del aparato genital, vistas entre 1970 y 1984. Se registró un caso por cada 555 mujeres hospitalizadas. Las anomalías genitales más frecuentes fueron tabique vaginal (25.9%), himen imporforado (17.2%), agenesia vaginal (12%), y quiste de Gartner (12%). También se halló agenesia uterina (8.8%), útero bicorne (6.9 %), útero didelfo (5.2%), hipoplasia uterina (5.2%), útero tabicado (1.7%) , hipertrofia del cérvix (1.7%), síndrome de Rokitansky (1.7%) y pseudohermafroditismo (1.7%). Como procedimientos de diagnóstico se efectuó laparotomías, lapa

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5

Jara-Vélez, Carlos Alberto, José Manuel Rengifo-Cruz, and Adriana Arango-Martínez. "Prevalencia de anomalías de los conductos de Müller en el Hospital General de Medellín (2000-2005)." Revista Colombiana de Obstetricia y Ginecología 57, no. 2 (2006): 82–87. http://dx.doi.org/10.18597/rcog.506.

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Objetivos: determinar la prevalencia y características clínicas de pacientes con malformaciones Müllerianas que consultan a un hospital de tercer nivel.Métodos: se realizó un estudio de corte transversal, en pacientes con diagnóstico de malformaciones Müllerianas, en el Hospital General de Medellín entre los años 2000 y 2005.Resultados: de un total de 1.450 pacientes que consultaron por urgencias, consulta externa ginecológica o se encontraban hospitalizadas, 39 cumplieron los criterios de inclusión, hallándose una prevalencia de 2,6%. Las malformaciones más frecuentes fueron: agenesia vaginal

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6

Hoyle Cox, Javier. "Cirugía en esterilidad. Cirugía de los problemas congénitos." Revista Peruana de Ginecología y Obstetricia 26, no. 1 (2015): 154–55. http://dx.doi.org/10.31403/rpgo.v26i1609.

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Problemas de malformaciones congénitas son causa frecuente de esterilidad, su solución está dentro del campo quirúrgico, en la mayor parte de las veces, exceptuándose aquéllas como la agenesia vaginal, uterina u ovárica que, por su condición, son irreversibles.

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7

Barbosa Ramírez, Gabriel Andrés, Luis Jorge Lombana, and Leila Quintero. "Síndrome de Mayer-von Rokitansky-Küster-Hauser." Universitas Médica 54, no. 2 (2013): 253–60. http://dx.doi.org/10.11144/javeriana.umed54-2.smro.

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Introducción: el síndrome de Mayer-von Rokitansky-Küster-Hauser (MRKH) ocurre aproximadamente en una de cada cinco mil mujeres nacidas vivas y es la causa más común de ausencia congénita de vagina.Método: se presentan dos casos manejados quirúrgicamente mediante corrección abdominoperineal con interposición de intestino, en conjunto por las especialidades de Ginecología Pediátrica y de la Adolescencia y Cirugía de Colon y Recto en el Hospital de San Ignacio. Dados los hallazgos clínicos y paraclínicos, se consideró que la mejor opción terapéutica para las pacientes era la realización de la neo

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8

Altez, Carlos, Ernesto Molina, Félix Ortega, and David Angulo. "Neovagina con revestimiento peritoneal por laparascopia." Revista Peruana de Ginecología y Obstetricia 59, no. 1 (2013): 55–57. http://dx.doi.org/10.31403/rpgo.v59i21.

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La agenesia vaginal o Síndrome de Mayer-Rokitansky es una rara anomalía congénita, cuya prevalencia aproximada es de 1 de cada 5 000 mujeres recién nacidas. El tratamiento de estos pacientes representa un reto para el cirujano; se requieren buenos resultados cosméticos y funcionales. Se presenta el caso de una paciente de 41 años con síndrome de Mayer-Rokitansky, a la cual se le construyó una neovagina asistida por laparoscopia, según la técnica de Davydov modificada. No hubo complicaciones inmediatas o mediatas. Se obtuvo una adecuada longitud de vagina, de 7 cm una semana después de la cirug

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9

Rechkemmer Prieto, Adolfo. "Creación laparoscópica de neovagina según técnica de Davydov modificado, en pacientes con síndrome de Rokitanski." Revista Medica Herediana 32, no. 1 (2021): 33–36. http://dx.doi.org/10.20453/rmh.v32i1.3945.

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Se describe una técnica quirúrgica alternativa para la formación de neovagina en ocho casos de agenesia de útero y vagina. Todas las pacientes tenían amenorrea primaria y ausencia congénita de útero y vagina (Síndrome de Rokitansky), y tenían entre 18 y 25 años de edad. De manera breve, la técnica consistió en hacer una disección roma en el espacio vésico-rectal hasta alcanzar el peritoneo. Se realizó tracción del peritoneo hacia abajo con una pinza, se abrió y se suturó con vicryl 0 al borde del orificio de la neovagina a nivel del introito. Por vía laparoscópica se cerró el peritoneo formand

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10

Martínez Martínez, C., AJ Láinez Ramos-Bossini, and B. Mirón Pozo. "Giant Gartner duct cyst: complications and management." Cirugía Andaluza 31, no. 2 (2020): 196–98. http://dx.doi.org/10.37351/2020312.27.

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Resumen La persistencia del quiste del conducto de Gartner es una entidad bastante infrecuente que consiste en la persistencia de un remanente del conducto de Wolff o mesonéfrico. Suelen estar localizados en el aspecto anterolateral de la vagina, pero pueden hallarse en cualquier localización de la pared vaginal. Pueden estar asociados a malformaciones nefrourológicas como uréter ectópico o agenesia o hipoplasia renal unilateral. Con frecuencia, los quistes del conducto de Gartner son pequeños y asintomáticos, pero si son lo suficientemente grandes pueden producir síntomas como dolor pélvico o

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11

Plasencia, W., M. A. Barber, I. Eguiluz, M. Lure, and J. A. García-Hernández. "Tratamiento de un hematómetra con sonda de Foley en un caso de agenesia vaginal." Progresos de Obstetricia y Ginecología 47, no. 11 (2004): 533–37. http://dx.doi.org/10.1016/s0304-5013(04)76049-5.

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12

Souza, Pedro Duran Marquez de, Laís Rodrigues Valadares, Vantuir José Domingos da Mota, Ana Thalissa Vilela Carvalho, and Sonaly Santiago Pereira. "importância do exame clínico no reconhecimento da síndrome de Herlyn-Werner-Wunderlich: relato de caso." Revista de Medicina 100, no. 2 (2021): 184–88. http://dx.doi.org/10.11606/issn.1679-9836.v100i2p184-188.

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A síndrome de Herlyn-Werner-Wunderlich (SHWW) é uma doença congênita rara dos ductos müllerianos, em que há útero didelfo, obstrução de hemivagina obstruída por septo e agenesia renal ipsilateral. A apresentação clínica mais comum é dor pélvica progressiva, dismenorreia e massa palpável. Em alguns casos a paciente pode apresentar menstruação normal devido a obstrução de apenas uma hemivagina, fato que resulta em atraso no diagnóstico. Relato do caso: Paciente, 13 anos, sexo feminino, com queixa de dor pélvica intermitente e progressiva, há um ano, associada a irregularidade menstrual, é atendi

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13

Adjoby, Cassou R., Soh V. Koffi, Denis Effoh, et al. "Mayer-Rokitansky-Kuster-Hauser syndrome and ovarian benign teratoma: a case report." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 9, no. 2 (2020): 815. http://dx.doi.org/10.18203/2320-1770.ijrcog20200383.

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Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH) is an unknown congenital etiology disorder characterized by agenesia or hypoplasia of the Müller ductal system, including the upper vagina, uterus and fallopian tubes. The occurrence of an associated ovarian tumor is rare, with fewer than 20 cases reported to date according to the literature. We report the case of a 14-year-old girl, virgin, who had not yet seen her menarche, complaining of an abdomino-pelvic mass associated with pain. The ultrasound performed revealed a large left ovarian tumor and an absence of uterus. The indication of a laparo

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14

Duarte Contreras, Alberto. "Valor semiológico de la secreción mucosa genital de la recién nacida." Revista Colombiana de Obstetricia y Ginecología 44, no. 2 (1993): 153–57. http://dx.doi.org/10.18597/rcog.844.

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Toda recién nacida a término debe presentar en los primeros días de vida una secreción mucosa en el vestíbulo vaginal.Esta secreción fisiológica no se encuentra:1- En las recién nacidas prematuras.2- En las recién nacidas a término con malformaciones congénitas que obstruyen la luz del canal genital.3- En recién nacidas a término con atresia o con agenesia del cérvix uterino.Estas malformaciones se pueden diagnosticar o al menos sospechar durante el período neonatal a partir de un "síntoma negativo", la falta de secreción cérvico vaginal en el introito vaginal.Los métodos de diagnóstico son la

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15

Prötzel Pinedo, Ana. "Amenorrea Primaria." Revista Peruana de Ginecología y Obstetricia 54, no. 3 (2015): 166–69. http://dx.doi.org/10.31403/rpgo.v54i1107.

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Las principales causas de amenorrea primaria incluyen el síndrome de Turner, el síndrome de insensibilidad androgénica y la agenesia útero-vaginal. Para el diagnóstico, es práctico relacionar este síntoma con el grado de desarrollo puberal, la talla y con la presencia o no de anormalidades en el tracto genital y es útil la siguiente clasificación, que será revisada desde el punto de vista genético: A)Amenorrea con retraso puberal: Hipogonadismo hipergonadotrópico: síndrome de Turner (ST), síndrome de Swyer (XYGD), síndrome de Perrault y otras formas de disgenesia gonadal XX (XXGD). Hipogonadis

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16

Macêdo, J. T. S. A., R. B. Lucena, P. R. Giaretta, et al. "Defeitos congênitos em bovinos da Região Central do Rio Grande do Sul." Pesquisa Veterinária Brasileira 31, no. 4 (2011): 297–306. http://dx.doi.org/10.1590/s0100-736x2011000400005.

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Foram revisados casos de defeitos congênitos (DCs) diagnosticados em bovinos no Laboratório de Patologia da Universidade Federal de Santa Maria em 1964-2010. Durante o período estudado, foram examinados materiais provenientes da necropsia de 7.132 bovinos e foram encontrados 31 bezerros (0,4%) com DCs, os quais foram classificados em 34 tipos e alocados nos sistemas orgânicos primariamente afetados. Os DCs ocorriam isoladamente (19 [61,3%]) ou afetavam múltiplos sítios anatômicos (15 [28,7%]) com frequência semelhante em ambos os sexos. Como vários terneiros mostraram múltiplos DCs, um total d

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17

Piriyev, Elvin, and Thomas Romer. "Rare case: enucleation of multiple fibroids after intraoperative vaginal sonographic detection of the solitary pelvic kidney by patient with Mayer-Rokitansky-Kuster-Hauser syndrome." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 9, no. 9 (2020): 3873. http://dx.doi.org/10.18203/2320-1770.ijrcog20203872.

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Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH) is a congenital anomaly of the genital tract that occurs in about 1 in 4000 women. MRKH syndrome can be associated with renal, skeletal, heart and hearing abnormalities. The frequency of renal/urinary tract abnormalities is 33%. Only a few cases of fibroid development in MRKH syndrome have been described in the literature. The diagnosis and surgery of a fibroid in MRKH syndrome may be complicated in associated kidney abnormality by an atypical kidney position, as in this case: pelvic kidney on one side and renal agenesia on the contralateral side.

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18

Cam, Cetim, Cem Celik, Mustafa Sakalli, Bahar Baykal, and Ates Karateke. "Introito-cervical sigmoid colon transpositioning procedure." Open Medicine 5, no. 2 (2010): 184–88. http://dx.doi.org/10.2478/s11536-008-0041-y.

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AbstractThe reported incidence of vaginal agenesis varies from 1 in 4,000 to 1 in 80,000 and individuals with congenital absence of vagina usually are first seen by a gynecologist at ages 14 to 15 years, when the absence of menses causes concern. A colon-introitus anastomosis was performed with interrupted absorbable sutures after opening peritoneum on müllerien dimple by sharp dissection using a guide inserted through the created perineo-abdominal tunnel. A rare case of vaginal agenesis with a septate uterus and normal tubes and ovaries is reported. Sigmoid vaginoplasty seemed the most approp

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19

Figueroa-Blanco, Andrés Felipe, and Miguel Ángel Montañez-Aldana. "Herlyn-Werner-Wünderlinch syndrome: case report." Case reports 4, no. 2 (2018): 111–17. http://dx.doi.org/10.15446/cr.v4n2.69279.

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Introducción. El síndrome de Herlyn-Werner-Wünderlich (HWW) es una asociación de tres alteraciones anatómicas urogenitales de baja incidencia. Las alteraciones müllerianas son poco comunes y suelen ser hallazgos incidentales, por lo que se encuentran subdiagnosticadas y poco se conoce su génesis o su relación con tener más probabilidad de expresión en el lado derecho. Reporte de caso. Se trata de una paciente de 17 años quien consultó por dolor abdominal hipogástrico de fuerte intensidad ligado a sangrado fétido. En el examen físico se encontró tabique vaginal y en las imágenes complementarias

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20

Utama, Bobby Indra, and Ermawati Ermawati. "SEPTUM VAGINA TRANSVERSA." JOURNAL OBGIN EMAS 1, no. 2 (2019): 80–85. http://dx.doi.org/10.25077/aoj.1.2.80-85.2017.

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The vagina is a membranous muscular tube that connects the vulva and uterus. Congenital or congenital abnormalities in the form of complete or partial absence of the vagina (vaginal agenesis). Patients who experience vaginal agenesis have less frequency, namely 1 in 4000 births, 1 in 4000 to 10,000 births (ACOG). Meanwhile in Dr. Cipto Mangunkusumo Jakarta from 1995 to 1999, an average of 10-12 cases per year. It has been reported the case of a female patient aged 14 years who entered the Gynecology Ward Dr. M. Djamil Padang on January 25, 2014 at 11.00 WIB with a delivery from the RSMJ gyn cl

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21

Razak, Lubna, and Raheela Mohsin. "Primary Menouria due to Congenital Urethrovaginal Fistula with Vaginal Agenesis." Nepal Journal of Obstetrics and Gynaecology 13, no. 2 (2018): 63–65. http://dx.doi.org/10.3126/njog.v13i2.21704.

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Congenital Urethrovaginal fistula with vaginal agenesis is a rare variant of vaginal agenesis. It is difficult to diagnose, classify and treat because of late clinical presentation at menarche. Management is usually challenging, and it involves vaginal reconstruction. A 22 years female presented with cyclical menouria since age of 12 years. Clinical examination revealed the absence of a vagina with developed secondary sexual characters such as axillary and pubic hair, breast development. Abdominal USG showed normal uterus and ovaries, urinary bladder with left kidney. MRI revealed functi

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22

Agarwal, Mukta, Bhawana Tiwary, and Prajnanika Gurung. "Complex mullarian duct abnormality in a young female: a theraputic dilemma." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 6, no. 8 (2017): 3673. http://dx.doi.org/10.18203/2320-1770.ijrcog20173510.

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Genital outflow tract obstruction is a rare cause of primary amenorrhoea. Cervical agenesis is a very rare condition often associated with atresia of vagina. Clinical diagnosis is usually difficult before surgery. Transverse vaginal septum or vaginal agenesis is also a rare condition that results from incomplete fusion between vaginal components of the mullerian ducts and urogenital sinus. If the septum is complete, the menstrual flow will be obstructed causing primary amenorrhoea. The septum is basically a membrane of fibrous connective tissue with both muscular and vascular components formed

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23

LNU, Pushpalatha, O. Syamala, Rukshana LNU, K. Sangeetha, and G. Usha Rani. "Vaginal Reconstruction in Müllerian Agenesis with User- Friendly Indigenous Prosthetic Vaginal Dilators." Journal of SAFOMS 2, no. 2 (2014): 75–78. http://dx.doi.org/10.5005/jp-journals-10032-1046.

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ABSTRACT Objective Vaginal reconstruction in Müllerian agenesis through nonsurgical method, using serial vaginal dilators which were worn by the patients with the help of a T-shaped perineal bandage. Materials and methods Seven patients with Müllerian agenesis had attended the outpatient clinic between 2008 and 2013. The age of women ranged from 18 to 30 years. This clinical report describes the use of prosthesis, fabricated by a maxillofacial prosthodontist that enabled the patients to have custom made personalized vaginal dilators of increasing dimensions which they could wear with comfort w

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24

Tharihalli, Chandrashekhar, Muralikrishna V., and Shiva Kumar H. C. "Surgical management of vaginal agenesis using a modified Mc Indoe’s technique: VIMS experience." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 6, no. 9 (2017): 3841. http://dx.doi.org/10.18203/2320-1770.ijrcog20173683.

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Background: Mullerian agenesis is a challenge to reconstructive surgeons. In order to create a new vagina that mimic the normal one in size, lining and appearance, multiple techniques have been designed; among these techniques Mc Indoe’s vaginoplasty represents the simplest one with good results. Mc Indoe’s operation which involves the creation of a space between bladder and rectum, insertion of a mould covered with split-thickness skin graft into that neo-vaginal space, and use of postoperative vaginal mould for dilation and to avoid stenosis. However, many modifications have been introduced

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Park, CH, and CH Son. "Segmental agenesis of the uterine body, cervix and vagina in a bitch." Veterinární Medicína 64, No. 03 (2019): 134–37. http://dx.doi.org/10.17221/139/2018-vetmed.

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This report describes a case of congenital segmental agenesis of the uterine body, cervix and vagina in a bitch. A five-year-old, Pomeranian bitch was presented with anorexia, abdominal distension and absence of the oestrus vulvar discharge. Complementary examinations were performed and ultrasonography revealed marked distention of the uterine horns with fluid-filled thin wall and defects in the uterine-vaginal segment. During surgery, closer inspection of the reproductive tract showed segmental agenesis of the uterine body, cervix and cranial part of vagina. The dog recovered uneventfully and

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Ali Adwal Ali, Khalida M. Amin, Emil N. AZZO, and Ayla K. Kahya. "Absent vagina a description of cases with varied ages, presentations and reconstructions." International Journal of Research in Pharmaceutical Sciences 10, no. 3 (2019): 1741–45. http://dx.doi.org/10.26452/ijrps.v10i3.1365.

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The aim is to describe cases of vaginal agenesis of varied ages presentations and managements and report the outcome of interventions regarding restoration of continuity of reproductive tract and normal sexual activity. A prospective descriptive case series study. Five female patients with vaginal agenesis were recruited from November 2005 to November 2016. Three were adolescents and had a functioning uterus. Three patients underwent vaginoplasty using McIndoe method, one had vagino-vaginal anastomosis, and the other had hysterectomy to remove source of menstruation. Age ranged from 12 to 24 y

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27

Barreno Sánchez, Diana Fernanda, Luis Geovanny Paguay Carrasco, and Mariuxi López. "Síndrome de Herlyn-Wener-Wunderlich." Mediciencias UTA 3, no. 4 (2019): 39. http://dx.doi.org/10.31243/mdc.uta.v3i4.238.2019.

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Introducción: El Síndrome de Herlyn-Wener-Wunderlich es una malformación de los conductos de Müller y de Wolf, debido a una falta de fusión de los mismos, es muy rara y se caracteriza por presentar un útero didelfo, con una hemivagina obstruida y agenesia renal ipsilateral, más frecuente del lado derecho. Objetivo: Describir un caso clínico de una paciente adolescente con cuadro de dismenorrea secundario a Sindrome de Herlyn-Wener-Wunderlich. Material y métodos: Se realizó un estudio descriptivo, retrospectivo y documental sobre dismenorrea secundaria, malformaciones mullerianas y

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28

Sultana, Razia, Nazmul Haque, and Ferdousi Begum. "Effective uterovaginal anastomosis done in cervical agenesis with menouria." Bangladesh Medical Journal Khulna 46, no. 1-2 (2014): 28–30. http://dx.doi.org/10.3329/bmjk.v46i1-2.18237.

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Agenesis of the uterine cervix is uncommon uterine anomaly. We report a case of 22 year old woman who was admitted in a private hospital with menouria and pelvic mass. Examination found no communication between vagina and uterus. Cervix was absent. Utero-vaginal anastomosis was done and a Foleys catheter was inserted in the uterine cavity for 14 days. During follow up of 1 month and 6 month after surgery patient was menstruating normally and examination revealed that the communication between the uterus and vagina was healed and had been sexually active at 6 months after the procedure. So uter

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29

Perlman, Sally, and S. Paige Hertweck. "Vaginal Agenesis." Journal of Pediatric and Adolescent Gynecology 13, no. 3 (2000): 143–44. http://dx.doi.org/10.1016/s1083-3188(00)00051-6.

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30

Symonds, E. M. "Vaginal agenesis." Current Obstetrics & Gynaecology 1, no. 3 (1991): 154–57. http://dx.doi.org/10.1016/0957-5847(91)90065-6.

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31

Kamal, Samarina, Sarita Tirkey, Shashibala Singh, and Shobha Chakraborty. "A clinical study of McIndoe vaginoplasty in vaginal agenesis." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 8, no. 12 (2019): 4732. http://dx.doi.org/10.18203/2320-1770.ijrcog20195310.

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Background: The aim of this study is to determine the effectiveness of McIndoe Vaginoplasty in the creation of a neovagina for patients with vaginal agenesis.Methods: this is a retrospective study of 50 cases of vaginal agenesis, who underwent McIndoe Vaginoplasty over a period of 8 years (2004-2012) by using skin graft in 25 cases and amnion as graft in the remaining.Results: McIndoe Vaginoplasty was performed successfully in all 50 patients and post-surgical result was acceptable to the patient psychologically, sexually and aesthetically.Conclusions: McIndoe Vaginoplasty is a safe and effect

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Patnana, Arun Kumar, Ankita Chugh, Vinay Kumar Chugh, and Shashank Shekhar. "Simple and novel technique for fabrication of prosthetic vaginal dilators." BMJ Case Reports 12, no. 4 (2019): e229524. http://dx.doi.org/10.1136/bcr-2019-229524.

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Vaginal agenesis is one of the major congenital anomalies affecting women. Postoperative prosthetic vaginal dilators are indicated in patients treated surgically for vaginal agenesis. Although different dental materials such as acrylics and silicone-coated materials are used, addition silicones alone have never been used for the fabrication of prosthetic vaginal dilators. Addition silicone materials have advantages, such as high elastic recovery, high tear and tensile strengths, which aid in the definitive use of vaginal dilators. Vaginal dilators fabricated using addition silicone materials a

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Mishra, Vineet, Suwa Ram Saini, Priyankur Roy, Rohina Aggarwal, Ruchika Verneker, and Shaheen Hokabaj. "Uterine conserving surgery in a case of cervicovaginal agenesis with cloacal malformation." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 6, no. 3 (2017): 1144. http://dx.doi.org/10.18203/2320-1770.ijrcog20170604.

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Cervico-vaginal agenesis (MRKHS) with normally formed uterus along with cloacal malformation is a very rare mullerian anomaly. We report a case, of a 13-year-old girl who was admitted at our tertiary care center with complaints of primary amenorrhea and cyclical lower abdominal pain for 3 months. Clinical examination and radiological investigations revealed complete cervico-vaginal agenesis with normal uterus with hematometra with horse shoe kidney. Vaginoplasty was done by McIndoe’s method with uterovaginal anastomosis and neocervix formation. Malecot’s catheter was inserted in uterine cavity

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Avino, Adelaida, Laura Răducu, Adrian Tulin, et al. "Vaginal Reconstruction in Patients with Mayer–Rokitansky–Küster–Hauser Syndrome—One Centre Experience." Medicina 56, no. 7 (2020): 327. http://dx.doi.org/10.3390/medicina56070327.

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Background and Objectives: The Mayer–Rokitansky–Küster–Hauser syndrome is a congenital condition in which patients are born with vaginal and uterus agenesis, affecting the ability to have a normal sexual life and to bear children. Vaginal reconstruction is a challenging procedure for plastic surgeons. The aim of this study is to report our experience in the management of twelve patients with congenital absence of the vagina due to the MRKH syndrome. Materials and Methods: We performed a retrospective study on 12 patients admitted to the Plastic Surgery Department of the Clinical Emergency Hosp

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Mohamed, Kasim, Preetha Krishnamurthy, Yogitha K, and Syed Altaf Hussain. "Hollow Prosthetic Vaginal Dilator - A Novel Technique." Journal of Evolution of Medical and Dental Sciences 10, no. 11 (2021): 841–44. http://dx.doi.org/10.14260/jemds/2021/180.

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Certain rare congenital defects can occur during the prenatal development of the female reproductive system, resulting in an abnormal or absent vagina.1 It is a part of the female genital tract. It is muscular and an elastic organ with a soft epithelial lining making it susceptible to disruption during crucial times of organogenesis.1,2 There are different malformations that occur in the female genital organ, many of which are classified under the broader term “Müllerian duct anomalies”. 1,2 Müllerian agenesis is also referred to as congenital absence of the uterus and vagina (CAUV), müllerian

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Muralidhar, Lakshmidevi, and Pramila Pandey. "Partial Vaginal Agenesis with Transverse Vaginal Septum." International Journal of Infertility & Fetal Medicine 5, no. 3 (2014): 110–12. http://dx.doi.org/10.5005/jp-journals-10016-1092.

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ABSTRACT Partial vaginal agenesis with transverse vaginal septum is rare malformation of female genital system. The reported incidence of vaginal atresia is 1:4000 to 5000 live female birth. The incidence of septum in upper one-third is 46%, middle 35%, lower 19%. Transverse vaginal septum occurs due to defect in vertical fusion of mullerian ducts during embryogenesis. Vaginal atresia occurs due to failure of canalization of sinovaginal bulbs. We are presenting such a rare case of partial vaginal agenesis with transverse vaginal septum. The aim of this presentation is to make the consideration

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Ghosh, T. S., and E. Y. Kwawukume. "Construction of an artificial vagina with sigmoid colon in vaginal agenesis." International Journal of Gynecology & Obstetrics 45, no. 1 (1994): 41–45. http://dx.doi.org/10.1016/0020-7292(94)90764-1.

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Albal, Manisha, Prasad Y. Bansod, and Mahendra Chauhan. "Neovagina creation using sigmoid colon in vaginal agenesis: a case report and review of literature." International Surgery Journal 7, no. 3 (2020): 904. http://dx.doi.org/10.18203/2349-2902.isj20200843.

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Mullerian duct anomalies are rare and can present with abnormalities in upper vagina, cervix, uterus, and fallopian tubes. The exact incidence of cervicovaginal agenesis is unknown and there are very few cases recorded in the literature. Authors report a 12-year-old girl referred from gynaecologist with chronic cyclical abdominal pain with underdeveloped, geniatilia and developed secondary sexual characters. Radiological investigations showed hypoplastic cervix with hematometra and left hemato salpinx. A definitive repair with creation of a neovagina using a sigmoid colon segment was performed

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Oelschlager, Anne-Marie Amies, Katherine Debiec, and Heather Appelbaum. "Primary vaginal dilation for vaginal agenesis." Current Opinion in Obstetrics and Gynecology 28, no. 5 (2016): 345–49. http://dx.doi.org/10.1097/gco.0000000000000302.

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Hakim, Seema, Ayesha Ahmad, Maneesha Jain, and Afzal Anees. "Unilateral Functional Uterine Horn with Non Functioning Rudimentary Horn and Cervico-Vaginal Agenesis: Case Report." Bangladesh Journal of Medical Science 13, no. 1 (2014): 101–4. http://dx.doi.org/10.3329/bjms.v13i1.17500.

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Developmental anomalies involving Mullerian ducts are one of the most fascinating disorders in Gynaecology. The incidence rates vary widely and have been described between 0.1-3.5% in the general population. We report a case of a fifteen year old girl who presented with primary amenorrhea and lower abdomen pain, with history of instrumentation about two months back. She was found to have abdominal lump of sixteen weeks size uterus. On examination vagina was found to be represented as a small blind pouch measuring 2-3cms in length. A rectovaginal fistula (2x2 cms) was also observed. Ultrasonogr

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Calderón V., Rolando, Víctor Díaz H., and César Rutte C. "A propósito de un caso de agenesia de útero y vagina." Revista Peruana de Ginecología y Obstetricia 14, no. 2 (2015): 235–38. http://dx.doi.org/10.31403/rpgo.v14i1458.

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La agenesia de vagina ha sido recientemente reportada en nuestro medio y la agenesia de útero y del tercio superior de vagina se ve con cierta frecuencia. Hay que recordar que embriológicamente los dos tercios inferiores de la vagina se desarrollan a partir del seno urogenital, mientras que el tercio superior: el útero y las trompas se desarrollan a partir del conducto de Muller.

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Nakhal, Rola S., and Sarah M. Creighton. "Management of Vaginal Agenesis." Journal of Pediatric and Adolescent Gynecology 25, no. 6 (2012): 352–57. http://dx.doi.org/10.1016/j.jpag.2011.06.003.

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Özkan, Özlenen, Münire Erman Akar, Ömer Özkan, and N. Utku Doğan. "Reconstruction of Vaginal Agenesis." Annals of Plastic Surgery 66, no. 6 (2011): 673–78. http://dx.doi.org/10.1097/sap.0b013e3181edd50c.

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Edmonds, D. Keith. "Management of vaginal agenesis." Current Opinion in Obstetrics and Gynecology 25, no. 5 (2013): 382–87. http://dx.doi.org/10.1097/gco.0b013e328363d67f.

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Martadinata, Meiza, and Dedy Hendry. "Agenesis Serviks." JOURNAL OBGIN EMAS 3, no. 1 (2019): 70–75. http://dx.doi.org/10.25077/aoj.3.1.70-75.2019.

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Background : Cervical agenesis is an extremely rare congenital anomaly of female reproductive system with manifestation on the absence of uterine cervix with normal development of uterine and secondary sex signs. According to the American Fertility Society, cervical agenesis is classified as type IB Müllerian anomaly. Symptoms are include primary amenorrhea, cyclic abdominal lower pain and infertility.Objective : To report the treatment of cervical agenesis.Case Report : Reportedly, a woman, 28 years old, came with complaints of primary amenorrhea, cyclic abdominal lower pain and 3 years of pr

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Sunyecz, Alec, Megan Snider, Elizabeth Minniear, Omar Duenas-Garcia, Amber Payton, and Robert Shapiro. "Herlyn-Werner-Wunderlich Syndrome: A Case Report on a Congenital Uterine Anomaly With Literature Review." Journal of Diagnostic Medical Sonography 37, no. 5 (2021): 492–98. http://dx.doi.org/10.1177/87564793211012633.

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During fetal development, abnormalities during Mullerian duct formation can lead to varied types of uterine, cervical, or vaginal anomalies. Herlyn-Werner-Wunderlich Syndrome (HWWS) is a rare, congenital Mullerian duct anomaly characterized by the triad of uterine didelphys, obstructed hemi-vagina, and ipsilateral renal agenesis. If the diagnosis is delayed or missed, permanent sequalae such as chronic pain, infection, and infertility can result. This is a case of a 16-year-old woman with heavy vaginal bleeding and menstrual cramping in which sonography was used in the diagnosis of HWWS. Sonog

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Skerritt, Clare, Alejandra Vilanova Sánchez, Victoria Lane, et al. "Menstrual, Sexual, and Obstetrical Outcomes after Vaginal Replacement for Vaginal Atresia Associated with Anorectal Malformation." European Journal of Pediatric Surgery 27, no. 06 (2016): 495–502. http://dx.doi.org/10.1055/s-0036-1593610.

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Background The authors of this article became aware of significant differences in the management of two females with a rectovestibular fistula and associated vaginal agenesis. In one patient, a sigmoid colovaginoplasty was performed at the time of the posterior sagittal anorectoplasty (PSARP), and the other underwent repair of the rectovestibular fistula with a primary PSARP, but the surgeons elected to delay the timing of vaginal reconstruction. We decided to review the literature, to establish if recommendations could be made to optimize the management of these children based on current evid

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Tugues, Mireia, Bernardo Nuñez, and Raquel Corripio. "Vaginal bleeding in a misdiagnosed Mayer-Rokitansky-Küster-Hauser syndrome." BMJ Case Reports 14, no. 4 (2021): e241387. http://dx.doi.org/10.1136/bcr-2020-241387.

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The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, a spectrum of anomalies arising from incomplete development of the Müllerian ducts, is characterised by congenital aplasia of the uterus and upper part of the vagina, often in the absence of other phenotypical abnormalities. We report the case of a 13-year-old girl referred to our endocrinology unit after an incidental finding of uterine agenesis during laparoscopy to correct suspected ovarian torsion. Initial transabdominal ultrasonography found no uterus. Given her normal secondary sex characteristics, karyotype and hormone profile, MRKH sy

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Fliegner, John R. H. "Vaginal Agenesis and the Embryology of Vaginal Epithelium." Australian and New Zealand Journal of Obstetrics and Gynaecology 34, no. 5 (1994): 562–66. http://dx.doi.org/10.1111/j.1479-828x.1994.tb01111.x.

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Eizenberg, Norman, Seong-Seng Tan, Diane Alcorn, and Felix Beck. "Vaginal Agenesis and the Embryology of Vaginal Epithelium." Australian and New Zealand Journal of Obstetrics and Gynaecology 34, no. 5 (1994): 565–66. http://dx.doi.org/10.1111/j.1479-828x.1994.tb01112.x.

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