Retronucal cystic hygroma as a marker of chromosomal abnormalities in the first trimester of gestation - Update
Descripción del Articulo
Objective: To evaluate the association of retronucal cystic hygroma (RCH) and fetal chromosomal abnormalities. Methods: Retrospective observational study of 323 first trimester fetuses at risk for chromosomal abnormalities diagnosed by ultrasound between 11 and 13.6 weeks. Results: Of 323 fetuses at...
| Autores: | , , , , |
|---|---|
| Formato: | artículo |
| Fecha de Publicación: | 2022 |
| Institución: | Sociedad Peruana de Obstetricia y Ginecología |
| Repositorio: | Revista Peruana de Ginecología y Obstetricia |
| Lenguaje: | español inglés |
| OAI Identifier: | oai:ginecologiayobstetricia.pe:article/2423 |
| Enlace del recurso: | https://ginecologiayobstetricia.pe/index.php/RPGO/article/view/2423 |
| Nivel de acceso: | acceso abierto |
| Materia: | Higroma quístico retronucal Translucencia nucal tabicada Biopsia de vellosidades coriales Amniocentesis Aberraciones cromosómicas |
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Revista Peruana de Ginecología y Obstetricia |
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Retronucal cystic hygroma as a marker of chromosomal abnormalities in the first trimester of gestation - Update Higroma quístico retronucal como marcador de anomalías cromosómicas en el primer trimestre de la gestación - Actualización |
| title |
Retronucal cystic hygroma as a marker of chromosomal abnormalities in the first trimester of gestation - Update |
| spellingShingle |
Retronucal cystic hygroma as a marker of chromosomal abnormalities in the first trimester of gestation - Update Huamán Guerrero, Moisés Higroma quístico retronucal Translucencia nucal tabicada Biopsia de vellosidades coriales Amniocentesis Aberraciones cromosómicas |
| title_short |
Retronucal cystic hygroma as a marker of chromosomal abnormalities in the first trimester of gestation - Update |
| title_full |
Retronucal cystic hygroma as a marker of chromosomal abnormalities in the first trimester of gestation - Update |
| title_fullStr |
Retronucal cystic hygroma as a marker of chromosomal abnormalities in the first trimester of gestation - Update |
| title_full_unstemmed |
Retronucal cystic hygroma as a marker of chromosomal abnormalities in the first trimester of gestation - Update |
| title_sort |
Retronucal cystic hygroma as a marker of chromosomal abnormalities in the first trimester of gestation - Update |
| dc.creator.none.fl_str_mv |
Huamán Guerrero, Moisés Pacheco Romero, José Espinoza Llanos, Lourdes Huamán Joo, Moisés Díaz Kuan, Alicia |
| author |
Huamán Guerrero, Moisés |
| author_facet |
Huamán Guerrero, Moisés Pacheco Romero, José Espinoza Llanos, Lourdes Huamán Joo, Moisés Díaz Kuan, Alicia |
| author_role |
author |
| author2 |
Pacheco Romero, José Espinoza Llanos, Lourdes Huamán Joo, Moisés Díaz Kuan, Alicia |
| author2_role |
author author author author |
| dc.subject.none.fl_str_mv |
Higroma quístico retronucal Translucencia nucal tabicada Biopsia de vellosidades coriales Amniocentesis Aberraciones cromosómicas |
| topic |
Higroma quístico retronucal Translucencia nucal tabicada Biopsia de vellosidades coriales Amniocentesis Aberraciones cromosómicas |
| description |
Objective: To evaluate the association of retronucal cystic hygroma (RCH) and fetal chromosomal abnormalities. Methods: Retrospective observational study of 323 first trimester fetuses at risk for chromosomal abnormalities diagnosed by ultrasound between 11 and 13.6 weeks. Results: Of 323 fetuses at risk for chromosomal abnormalities, 132 cases of chromosomal abnormalities were found (40.9%). A total of 145 cases of RCH were identified; chorionic villus biopsy was performed in 64 (56.6%) and amniocentesis in 81 (43.5%); an abnormal karyotype was found in 82 (56.6%). Of 88 fetuses with isolated RCH, 33 (37.5%) had some chromosomal abnormality. In 58 fetuses with RCH associated with other abnormal findings, chromosomal abnormalities were found in 43 fetuses (74.1%) and of these 24 (41.4%) had abnormal ductus venosus flow wave (DVF), 17 (29.3%) had generalized edema, 8 cases (13.8%) with cardiopathy, 7 (12,1%) with absent nasal bone. The predictive values of RCH were sensitivity (S) 62.1%, specificity (Sp) 67%, positive predictive value (PPV) 56.6%, negative predictive value (NPV) 71.9%, p<0.001, OR: 3.3. RCH associated with other abnormal findings were S 52.4%, Sp 76.2%, PPV 76.2%, OR: 3.5, LR+: 2.2, p<0.000. Generalized edema and abnormal ductus venosus had the highest predictive values: PPV 88.2% and 83.3%, respectively. The most frequently found chromosomal abnormalities were T21 (53.7%), monosomy X (18.3%), T18 (15.9%), T13 (6.1%). Conclusions: Retronucal cystic hygroma is a risk marker with high predictive value for chromosomal abnormalities, being higher when associated with other abnormal ultrasound findings. Ultrasonographic identification of RCH in first trimester prenatal screening should be an indication to recommend diagnostic testing for chromosomal abnormalities. |
| publishDate |
2022 |
| dc.date.none.fl_str_mv |
2022-07-11 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
| dc.identifier.none.fl_str_mv |
https://ginecologiayobstetricia.pe/index.php/RPGO/article/view/2423 10.31403/rpgo.v68i2423 |
| url |
https://ginecologiayobstetricia.pe/index.php/RPGO/article/view/2423 |
| identifier_str_mv |
10.31403/rpgo.v68i2423 |
| dc.language.none.fl_str_mv |
spa eng |
| language |
spa eng |
| dc.relation.none.fl_str_mv |
https://ginecologiayobstetricia.pe/index.php/RPGO/article/view/2423/2627 https://ginecologiayobstetricia.pe/index.php/RPGO/article/view/2423/2628 |
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https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
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https://creativecommons.org/licenses/by/4.0 |
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openAccess |
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application/pdf application/pdf |
| dc.publisher.none.fl_str_mv |
Sociedad Peruana de Obstetricia y Ginecología |
| publisher.none.fl_str_mv |
Sociedad Peruana de Obstetricia y Ginecología |
| dc.source.none.fl_str_mv |
The Peruvian Journal of Gynecology and Obstetrics ; Vol. 68 No. 2 (2022) Revista Peruana de Ginecología y Obstetricia; Vol. 68 Núm. 2 (2022) 2304-5132 2304-5124 reponame:Revista Peruana de Ginecología y Obstetricia instname:Sociedad Peruana de Obstetricia y Ginecología instacron:SPOG |
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Sociedad Peruana de Obstetricia y Ginecología |
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SPOG |
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SPOG |
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Revista Peruana de Ginecología y Obstetricia |
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Revista Peruana de Ginecología y Obstetricia |
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1868078736568483840 |
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Retronucal cystic hygroma as a marker of chromosomal abnormalities in the first trimester of gestation - UpdateHigroma quístico retronucal como marcador de anomalías cromosómicas en el primer trimestre de la gestación - ActualizaciónHuamán Guerrero, MoisésPacheco Romero, JoséEspinoza Llanos, LourdesHuamán Joo, MoisésDíaz Kuan, AliciaHigroma quístico retronucalTranslucencia nucal tabicadaBiopsia de vellosidades corialesAmniocentesisAberraciones cromosómicasObjective: To evaluate the association of retronucal cystic hygroma (RCH) and fetal chromosomal abnormalities. Methods: Retrospective observational study of 323 first trimester fetuses at risk for chromosomal abnormalities diagnosed by ultrasound between 11 and 13.6 weeks. Results: Of 323 fetuses at risk for chromosomal abnormalities, 132 cases of chromosomal abnormalities were found (40.9%). A total of 145 cases of RCH were identified; chorionic villus biopsy was performed in 64 (56.6%) and amniocentesis in 81 (43.5%); an abnormal karyotype was found in 82 (56.6%). Of 88 fetuses with isolated RCH, 33 (37.5%) had some chromosomal abnormality. In 58 fetuses with RCH associated with other abnormal findings, chromosomal abnormalities were found in 43 fetuses (74.1%) and of these 24 (41.4%) had abnormal ductus venosus flow wave (DVF), 17 (29.3%) had generalized edema, 8 cases (13.8%) with cardiopathy, 7 (12,1%) with absent nasal bone. The predictive values of RCH were sensitivity (S) 62.1%, specificity (Sp) 67%, positive predictive value (PPV) 56.6%, negative predictive value (NPV) 71.9%, p<0.001, OR: 3.3. RCH associated with other abnormal findings were S 52.4%, Sp 76.2%, PPV 76.2%, OR: 3.5, LR+: 2.2, p<0.000. Generalized edema and abnormal ductus venosus had the highest predictive values: PPV 88.2% and 83.3%, respectively. The most frequently found chromosomal abnormalities were T21 (53.7%), monosomy X (18.3%), T18 (15.9%), T13 (6.1%). Conclusions: Retronucal cystic hygroma is a risk marker with high predictive value for chromosomal abnormalities, being higher when associated with other abnormal ultrasound findings. Ultrasonographic identification of RCH in first trimester prenatal screening should be an indication to recommend diagnostic testing for chromosomal abnormalities.Objetivo. Evaluar la asociación del higroma quístico retronucal (HQR) y anomalías cromosómicasfetales. Métodos. Estudio observacional retrospectivo de 323 fetos del primer trimestre con riesgopara anomalías cromosómicas diagnosticados por ecografía entre las 11 y 13,6 semanas. Resultados.De 323 fetos con riesgo para anomalías cromosómicas, se encontró 132 casos de anomalíascromosómicas (40,9%). Se identificaron 145 casos de HQR; en 64 (56,6%) se realizó biopsia devellosidades coriales y en 81 (43,5%) amniocentesis, hallándose cariotipo anómalo en 82 (56,6%). De88 fetos con HQR aislado, 33 casos (37,5%) tuvieron alguna anomalía cromosómica; en 58 fetos conHQR asociado a otros hallazgos anormales, se encontró que en 43 fetos (74,1%) hubo anomalíascromosómicas, y de ellos 24 (41,4%) tenían onda de flujo (OVF) anormal del ductus venoso, 17(29,3%) tenían edema generalizado, 8 casos (13,8%) con cardiopatía, 7 (12,1%) ausencia del huesonasal. Los valores predictivos del HQR fueron: sensibilidad (S) 62,1%, especificidad (E) 67%, valorpredictivo positivo (VPP) 56,6%, valor predictivo negativo (VPN) 71,9%, p&lt;0,001, OR: 3,3. El HQRasociado a otros hallazgos anormales, tuvo los siguientes valores predictivos: S 52,4%, E 76,2%, VPP76,2%, OR: 3,5, LR+: 2,2, p&lt;0,000. El edema generalizado y el ductus venoso anormal tuvieron losvalores predictivos más altos: VPP 88,2% y 83,3%, respectivamente. Las anomalías cromosómicasencontradas con mayor frecuencia fueron: T21 (53,7%), monosomía X (18,3%), T18 (15,9%), T13(6,1%). Conclusiones. El higroma quístico retronucal es un marcador de riesgo con alto valorpredictivo para anomalías cromosómicas, siendo mayor cuando está asociado a otros hallazgosecográficos anormales. La identificación ecográfica del HQR en el tamizaje prenatal del primertrimestre debería ser indicación para recomendar una prueba diagnóstica para anomalíascromosómicas.Sociedad Peruana de Obstetricia y Ginecología2022-07-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttps://ginecologiayobstetricia.pe/index.php/RPGO/article/view/242310.31403/rpgo.v68i2423The Peruvian Journal of Gynecology and Obstetrics ; Vol. 68 No. 2 (2022)Revista Peruana de Ginecología y Obstetricia; Vol. 68 Núm. 2 (2022)2304-51322304-5124reponame:Revista Peruana de Ginecología y Obstetriciainstname:Sociedad Peruana de Obstetricia y Ginecologíainstacron:SPOGspaenghttps://ginecologiayobstetricia.pe/index.php/RPGO/article/view/2423/2627https://ginecologiayobstetricia.pe/index.php/RPGO/article/view/2423/2628Derechos de autor 2022 Moisés Huamán Guerrero, José Pacheco Romero, Lourdes Espinoza Llanos, Moisés Huamán Joo, Alicia Díaz Kuanhttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessoai:ginecologiayobstetricia.pe:article/24232026-01-12T15:22:08Z |
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13.408945 |
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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).