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1.
J Neonatal Perinatal Med ; 13(1): 91-96, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-31609706

RESUMEN

BACKGROUND: Renal pelvic dilatation (RPD) is a frequent finding in fetal ultrasound. The aim of the study is to correlate the prenatally detected moderate and severe pyelectasis with the postnatal outcome. METHODS: A retrospective analysis involving 90 cases of prenatally detected moderate and severe RPD referred to our prenatal diagnosis centre with 18 months of urological follow-up. Prenatal ultrasound was correlated with postnatal renal function, assessed by plasmatic creatinine and/or renal scintigraphy performed before surgery. RESULTS: Cases were divided between two groups according to postnatal management: group A including 35 newborns (38.9%) that needed surgical treatment and group B with 55 patients (61.1%) who were managed conservatively. The group A presented higher median RPD (18 mm, IQR 12-25 mm) compared to the group B (11 mm, IQR 10-14 mm). The most common anomaly detected within group A was pelvi-ureteric junction (PUI) obstruction (43%). Within group B 32 cases (58%) showed spontaneous resolution of hydronephrosis during postnatal follow up. In case of moderate pyelectasis the risk of postnatal surgery was 25% and raised to 60% for severe RPD. In our study, 29 newborns showed pathologic scintigraphies: 25 required surgery while 4 did not find indication for surgery due to ipsilateral renal function irreversible damage. 6 patients had high creatinine level (>0.6 mg/dl). 35 cases out of 90 (39%) developed monolateral irreversible renal function impairment. CONCLUSION: Moderate and severe RPD are often correlated with postnatal renal damage, therefore a close multidisciplinary follow-up is required. Prenatal scanning is highly predictive of postnatal outcome and can address properly the prenatal counseling.


Asunto(s)
Tratamiento Conservador , Hidronefrosis/terapia , Pielectasia/terapia , Obstrucción Ureteral/cirugía , Procedimientos Quirúrgicos Urológicos , Reflujo Vesicoureteral/terapia , Creatinina/metabolismo , Femenino , Humanos , Hidronefrosis/complicaciones , Hidronefrosis/congénito , Hidronefrosis/diagnóstico por imagen , Recién Nacido , Pelvis Renal/cirugía , Masculino , Embarazo , Pielectasia/diagnóstico por imagen , Pielectasia/metabolismo , Cintigrafía , Remisión Espontánea , Insuficiencia Renal/congénito , Insuficiencia Renal/etiología , Insuficiencia Renal/metabolismo , Estudios Retrospectivos , Índice de Severidad de la Enfermedad , Riñón Único , Ultrasonografía Prenatal , Uréter/cirugía , Obstrucción Ureteral/congénito , Obstrucción Ureteral/diagnóstico por imagen , Estrechez Uretral/diagnóstico por imagen , Estrechez Uretral/metabolismo , Estrechez Uretral/terapia , Anomalías Urogenitales/diagnóstico por imagen , Anomalías Urogenitales/metabolismo , Anomalías Urogenitales/terapia , Reflujo Vesicoureteral/diagnóstico por imagen , Reflujo Vesicoureteral/metabolismo
2.
J Neonatal Perinatal Med ; 12(3): 339-343, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30883366

RESUMEN

OBJECTIVE: Ovarian cysts are relatively common prenatal findings in female fetuses. The aim of this study is to evaluate the ability of antenatal ultrasound in predicting spontaneous regression or a need for surgery. DESIGN: All cases of fetal ovarian cysts treated in our Department between 2007 and 2016 were included. Patients underwent a sonographic monitoring in utero and after birth until spontaneous or surgical resolution. Subjects were divided into two groups according to their postnatal management. Receiver-operating characteristics (ROC) curves were used to test the predictive ability for postnatal surgery of the cyst's mean and maximum diameters; their optimal cut off points were also determined. RESULTS: 38 cases of antenatally-detected fetal ovarian cysts were included. 12/38 cases underwent surgery (Group A). 26/38 cases were resolved spontaneously (Group B). Cyst size of those which were surgically excised significantly differed from those that regressed spontaneously. ROC curve pointed to 45 mm and 47 mm as optimal cut off points for the mean and the maximum cystic diameters, respectively. CONCLUSIONS: Cyst size and echo-structure seemed good predictors for prognosis after birth. The optimal cut off points of the cysts mean and maximum diameters in predicting postnatal surgery have been identified as 45 mm and 47 mm, respectively.


Asunto(s)
Quistes Ováricos/diagnóstico por imagen , Ultrasonografía Prenatal , Estudios de Casos y Controles , Estudios de Cohortes , Femenino , Humanos , Recién Nacido , Quistes Ováricos/cirugía , Embarazo , Pronóstico , Remisión Espontánea
3.
J Ultrasound ; 10(3): 139-42, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-23396677

RESUMEN

We describe the clinical and cerebral ultrasonographic features of a rare case of type 1 acrocephalosyndactyly (Apert syndrome). The patient was a newborn male whose twin had died in utero. Most cases of Apert syndrome are sporadic, although autosomal dominant inheritance has also been reported. Diagnosis is based on physical examination together with imaging data. Since Apert syndrome can give rise to numerous CNS abnormalities, affected newborns should undergo echoencephalography for more complete characterization of their malformations.

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