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1.
Prenat Diagn ; 37(10): 1033-1039, 2017 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-28809041

RESUMEN

OBJECTIVE: The objective of the study is to analyse the sonographic features, cytogenetic results and pregnancy outcomes in complex malformations involving the body wall in a large cohort of fetuses with regard to different definitions proposed in the literature. METHOD: A retrospective study on 96 fetuses with complex malformations comprising ventral wall, craniofacial structures, limbs and umbilical cord that were evaluated between 1997 and 2015. RESULTS: The most common sonographic finding was an extensive ventral wall defect (95.8%; 92/96) comprising liver (94.6%; 87/92), intestine (82.6%; 76/92), heart (17.4%; 16/92) and bladder (8.7%; 8/92). Acrania and encephalocoele were observed in 24 and 9 fetuses (25.0%, 24/96; 9.4%, 9/96), respectively. Limb anomalies were present in 54 fetuses (56.3%; 54/96). Rudimentary or absent umbilical cord was observed in 62 fetuses (64.6%; 62/96). In 79 fetuses, there were additional multiple structural anomalies detected prenatally. None of the currently used definitions encompasses all possible phenotypes of body wall defects present in our cohort. Chromosomal aberrations were seen in 8 out of 60 cases with conclusive cytogenetic result (13.3%, 8/60). CONCLUSION: Chromosomal anomalies are common, and karyotyping should be offered. There is a need for a more rigorous classification of complex malformations in order to better understand the underlying pathophysiology. © 2017 John Wiley & Sons, Ltd.


Asunto(s)
Anomalías Congénitas/diagnóstico por imagen , Anomalías Congénitas/embriología , Ultrasonografía Prenatal , Aberraciones Cromosómicas/embriología , Encefalocele/diagnóstico por imagen , Encefalocele/embriología , Femenino , Edad Gestacional , Cardiopatías Congénitas/diagnóstico por imagen , Cardiopatías Congénitas/embriología , Humanos , Intestinos/anomalías , Intestinos/diagnóstico por imagen , Intestinos/embriología , Deformidades Congénitas de las Extremidades/diagnóstico por imagen , Deformidades Congénitas de las Extremidades/embriología , Hígado/anomalías , Hígado/diagnóstico por imagen , Hígado/embriología , Defectos del Tubo Neural/diagnóstico por imagen , Defectos del Tubo Neural/embriología , Embarazo , Resultado del Embarazo , Estudios Retrospectivos , Cordón Umbilical/anomalías , Cordón Umbilical/diagnóstico por imagen , Vejiga Urinaria/anomalías , Vejiga Urinaria/embriología
2.
Prenat Diagn ; 35(11): 1093-6, 2015 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-26175315

RESUMEN

OBJECTIVE: The objective of this study is to determine the risk of aneuploidy, associated structural anomalies, and pregnancy outcome in the presence of prenatal double bubble sign detection. METHOD: We have performed a retrospective study on ultrasound reports and pregnancy outcomes in 42 fetuses with double bubble sign examined in our ultrasound department between 1998 and 2013. RESULTS: Additional major defects or aneuploidy markers were present in 24 fetuses. Chromosomal abnormalities occurred in 21 cases. There were 35 live births; two pregnancies ended in intrauterine fetal demise; five patients opted for termination of pregnancy because of additional anomalies or abnormal karyotype. Postnatal or postmortem verification revealed duodenal obstruction secondary to intrinsic or extrinsic cause in 40 cases; in one case, proximal jejunal atresia was diagnosed, and one neonate had normal bowel. CONCLUSIONS: Sonographic double bubble sign is associated with a significant rate of major anatomic defects, abnormal karyotype, and unfavorable pregnancy outcome. It is strongly indicative of duodenal obstruction.


Asunto(s)
Aneuploidia , Anomalías Congénitas/diagnóstico por imagen , Obstrucción Duodenal/diagnóstico por imagen , Adulto , Aberraciones Cromosómicas , Anomalías Congénitas/epidemiología , Obstrucción Duodenal/epidemiología , Femenino , Humanos , Recién Nacido , Embarazo , Resultado del Embarazo/epidemiología , Estudios Retrospectivos , Ultrasonografía Prenatal , Adulto Joven
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