RESUMEN
Prune-belly syndrome is a rare compound fetal anomaly, characterized by absence or hypoplasia of abdominal wall musculature associated with urinary tract abnormalities and cryptorchidism. The prenatal ultrasound diagnosis was based on the findings of a lower abdominal cystic echo caused by abnormal dilatation of the bladder, upward compression of small intestines and decreased amniotic fluid volume. We experienced a case of Prune-belly syndrome diagnosed by ultrasound in a 12 weeks fetus following to IVF-ET pregnancy. Termination was performed at 12 weeks and autopsy confirmed the distended bladder, absence of abdominal muscles and urethra. So, we reported this case with a brief review of literature.
Asunto(s)
Femenino , Masculino , Embarazo , Músculos Abdominales , Pared Abdominal , Líquido Amniótico , Autopsia , Criptorquidismo , Diagnóstico , Dilatación , Feto , Intestino Delgado , Diagnóstico Prenatal , Síndrome del Abdomen en Ciruela Pasa , Ultrasonografía , Uretra , Vejiga Urinaria , Sistema UrinarioRESUMEN
Actinomycosis is a rare disease in human and has variable clinical features, which make the diagnosis difficult. Actinomycosis may be confused with malignancy and other inflammatory diseases because of its infiltrative nature and its tendency to invade normal anatomic barriers. We have experienced a case of abdominal actinomycosis combined with ovarian mucinous cystadenocarcinoma and report this case with brief review of literatures.