Síndrome de Mayer-Rokitansky- Küster-Hauser. Reporte de dos casos.
Saved in:
| Title: | Síndrome de Mayer-Rokitansky- Küster-Hauser. Reporte de dos casos. |
|---|---|
| Alternate Title: | Mayer-Rokitansky-Küster-Hauser Syndrome: Two cases report. |
| Authors: | Ávila-Vergara, Marco Antonio1 mavila_v@uas.edu.mx, León-Álvarez, Damián Alfredo2, López-Villegas, Miriam Nayeli2, Quintero-Medrano, Samantha Melissa2, Angulo-Bueno, Gladys Fabiola2, Vadillo-Ortega, Felipe3 |
| Source: | Ginecología y Obstetricia de México. mar2015, Vol. 83 Issue 3, p199-205. 7p. 5 Black and White Photographs. |
| Subjects: | MAYER-Rokitansky-Kuster-Hauser syndrome, PRIMARY amenorrhea, UTERUS abnormalities, SCOLIOSIS, DIAGNOSTIC ultrasonic imaging, ABDOMINAL surgery, PATIENTS, THERAPEUTICS |
| Abstract (English): | Agenesia of the Müllerian ducts is a low-frequency congenital disease but with devastating effects on women's reproductive health. In this paper we present two cases of women affected by Mayer-Rokitansky-Küster-Hauser syndrome (MRKH). First case was a 17-year-old woman with aplasia of the upper vagina and absence of uterus. No other defects were found and was classified as type 1-MRKH. Second case was 18-year-old woman with absence of uterus, escoliosis and polycystic ovary syndrome, classified as type II-MRKH. Patients were seen at the Hospital with primary amenorrhea and fully developed secondary sexual characteristics. A clinical follow-up protocol, including the use of high-resolution image studies was used for diagnosis. Diagnostic procedures and current medical approaches to the treatment of MRKH are discussed, including psychological advisory, surgical procedures and new tissue-engineering techniques. [ABSTRACT FROM AUTHOR] |
| Abstract (Spanish): | La agenesia de los conductos de Müller es un padecimiento congénito poco frecuente pero de gran afectación. Se comunican dos casos de pacientes con síndrome de Mayer-Rokitansky-Küster-Hauser. El primer caso correspondió a una mujer de 17 años de edad con síndrome tipo 1, con aplasia de los dos tercios superiores de la vagina y ausencia de útero, sin otras alteraciones asociadas. El segundo caso es de una mujer de 18 años de edad con síndrome tipo 2 en la que se documentó ausencia de útero, escoliosis y síndrome de ovario poliquístico. El motivo de consulta fue: amenorrea primaria con desarrollo completo de characteres sexuales secundarios en ambos casos. Se utilizó un protocolo clínico para descartar diagnósticos diferenciales y se estableció el diagnóstico con ayuda de imagenología de alta resolución. Se discuten los procedimientos diagnósticos y tratamientos médicos actuales: atención psicológica, intervenciones quirúrgicas y técnicas de ingeniería de tejidos para formación de la neovagina. [ABSTRACT FROM AUTHOR] |
| Copyright of Ginecología y Obstetricia de México is the property of Federacion Mexicana de Ginecologia y Obstetricia and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | MedicLatina |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
|---|---|
| Header | DbId: lth DbLabel: MedicLatina An: 101849294 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Síndrome de Mayer-Rokitansky- Küster-Hauser. Reporte de dos casos. – Name: TitleAlt Label: Alternate Title Group: TiAlt Data: Mayer-Rokitansky-Küster-Hauser Syndrome: Two cases report. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Ávila-Vergara%2C+Marco+Antonio%22">Ávila-Vergara, Marco Antonio</searchLink><relatesTo>1</relatesTo><i> mavila_v@uas.edu.mx</i><br /><searchLink fieldCode="AR" term="%22León-Álvarez%2C+Damián+Alfredo%22">León-Álvarez, Damián Alfredo</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22López-Villegas%2C+Miriam+Nayeli%22">López-Villegas, Miriam Nayeli</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Quintero-Medrano%2C+Samantha+Melissa%22">Quintero-Medrano, Samantha Melissa</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Angulo-Bueno%2C+Gladys+Fabiola%22">Angulo-Bueno, Gladys Fabiola</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Vadillo-Ortega%2C+Felipe%22">Vadillo-Ortega, Felipe</searchLink><relatesTo>3</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Ginecología+y+Obstetricia+de+México%22">Ginecología y Obstetricia de México</searchLink>. mar2015, Vol. 83 Issue 3, p199-205. 7p. 5 Black and White Photographs. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22MAYER-Rokitansky-Kuster-Hauser+syndrome%22">MAYER-Rokitansky-Kuster-Hauser syndrome</searchLink><br /><searchLink fieldCode="DE" term="%22PRIMARY+amenorrhea%22">PRIMARY amenorrhea</searchLink><br /><searchLink fieldCode="DE" term="%22UTERUS+abnormalities%22">UTERUS abnormalities</searchLink><br /><searchLink fieldCode="DE" term="%22SCOLIOSIS%22">SCOLIOSIS</searchLink><br /><searchLink fieldCode="DE" term="%22DIAGNOSTIC+ultrasonic+imaging%22">DIAGNOSTIC ultrasonic imaging</searchLink><br /><searchLink fieldCode="DE" term="%22ABDOMINAL+surgery%22">ABDOMINAL surgery</searchLink><br /><searchLink fieldCode="DE" term="%22PATIENTS%22">PATIENTS</searchLink><br /><searchLink fieldCode="DE" term="%22THERAPEUTICS%22">THERAPEUTICS</searchLink> – Name: Abstract Label: Abstract (English) Group: Ab Data: Agenesia of the Müllerian ducts is a low-frequency congenital disease but with devastating effects on women's reproductive health. In this paper we present two cases of women affected by Mayer-Rokitansky-Küster-Hauser syndrome (MRKH). First case was a 17-year-old woman with aplasia of the upper vagina and absence of uterus. No other defects were found and was classified as type 1-MRKH. Second case was 18-year-old woman with absence of uterus, escoliosis and polycystic ovary syndrome, classified as type II-MRKH. Patients were seen at the Hospital with primary amenorrhea and fully developed secondary sexual characteristics. A clinical follow-up protocol, including the use of high-resolution image studies was used for diagnosis. Diagnostic procedures and current medical approaches to the treatment of MRKH are discussed, including psychological advisory, surgical procedures and new tissue-engineering techniques. [ABSTRACT FROM AUTHOR] – Name: Abstract Label: Abstract (Spanish) Group: Ab Data: La agenesia de los conductos de Müller es un padecimiento congénito poco frecuente pero de gran afectación. Se comunican dos casos de pacientes con síndrome de Mayer-Rokitansky-Küster-Hauser. El primer caso correspondió a una mujer de 17 años de edad con síndrome tipo 1, con aplasia de los dos tercios superiores de la vagina y ausencia de útero, sin otras alteraciones asociadas. El segundo caso es de una mujer de 18 años de edad con síndrome tipo 2 en la que se documentó ausencia de útero, escoliosis y síndrome de ovario poliquístico. El motivo de consulta fue: amenorrea primaria con desarrollo completo de characteres sexuales secundarios en ambos casos. Se utilizó un protocolo clínico para descartar diagnósticos diferenciales y se estableció el diagnóstico con ayuda de imagenología de alta resolución. Se discuten los procedimientos diagnósticos y tratamientos médicos actuales: atención psicológica, intervenciones quirúrgicas y técnicas de ingeniería de tejidos para formación de la neovagina. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Ginecología y Obstetricia de México is the property of Federacion Mexicana de Ginecologia y Obstetricia and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=lth&AN=101849294 |
| RecordInfo | BibRecord: BibEntity: Languages: – Code: spa Text: Spanish PhysicalDescription: Pagination: PageCount: 7 StartPage: 199 Subjects: – SubjectFull: MAYER-Rokitansky-Kuster-Hauser syndrome Type: general – SubjectFull: PRIMARY amenorrhea Type: general – SubjectFull: UTERUS abnormalities Type: general – SubjectFull: SCOLIOSIS Type: general – SubjectFull: DIAGNOSTIC ultrasonic imaging Type: general – SubjectFull: ABDOMINAL surgery Type: general – SubjectFull: PATIENTS Type: general – SubjectFull: THERAPEUTICS Type: general Titles: – TitleFull: Síndrome de Mayer-Rokitansky- Küster-Hauser. Reporte de dos casos. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ávila-Vergara, Marco Antonio – PersonEntity: Name: NameFull: León-Álvarez, Damián Alfredo – PersonEntity: Name: NameFull: López-Villegas, Miriam Nayeli – PersonEntity: Name: NameFull: Quintero-Medrano, Samantha Melissa – PersonEntity: Name: NameFull: Angulo-Bueno, Gladys Fabiola – PersonEntity: Name: NameFull: Vadillo-Ortega, Felipe IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: mar2015 Type: published Y: 2015 Identifiers: – Type: issn-print Value: 03009041 Numbering: – Type: volume Value: 83 – Type: issue Value: 3 Titles: – TitleFull: Ginecología y Obstetricia de México Type: main |
| ResultId | 1 |
