Retronucal cystic hygroma as a marker of chromosomal abnormalities in the first trimester of gestation - Update

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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...

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Autores: Huamán Guerrero, Moisés, Pacheco Romero, José, Espinoza Llanos, Lourdes, Huamán Joo, Moisés, Díaz Kuan, Alicia
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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network_name_str Revista Peruana de Ginecología y Obstetricia
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dc.title.none.fl_str_mv 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
format article
status_str 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
dc.rights.none.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 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
instname_str Sociedad Peruana de Obstetricia y Ginecología
instacron_str SPOG
institution SPOG
reponame_str Revista Peruana de Ginecología y Obstetricia
collection Revista Peruana de Ginecología y Obstetricia
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spelling 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<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<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
score 13.408945
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