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Isolated Fetal Ascites Secondary to Persistent Urogenital Sinus

机译:继发于持续性泌尿生殖窦的孤立胎儿腹水

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Objective. To present a case of isolated ascites secondary due to urogenital abnormalities (urogenital sinus) without any other prenatal ultrasound marker.Method. A 36-year-old woman with prenatal isolated ascites delivered a female baby, weighing 2.285 g; ascites was drained at birth and the baby underwent several episodes of urinary retention prior to undergoing X-ray investigations.Results. A voiding cystourethrogram revealed a short urogenital sinus: a vesicostomy was performed. A vaginoscopy revealed double vagina with a large posterior vagina. A posterior sagittal anorectal pull-through with genitoplasty was performed at 2 years old with 1-year follow-up.Conclusions. Though rare, a urogenital abnormality is to be suspected in fetal ascites cases with negative viral tests and no cardiac anomalies. The most common ultrasound marker of such abnormalities (fluid filled cavity) may be missing because of complete drainage of urine through the tubes into peritoneum.
机译:目的。提出一例因泌尿生殖系统异常(泌尿生殖窦)而继发的孤立性腹水的病例,无任何其他产前超声标记物。一名36岁产前腹水的妇女分娩了一名女婴,体重为2.285微克;出生时腹水被排出,婴儿在进行X射线检查之前经历了几次尿retention留。膀胱尿道造影图显示尿道窦短:行膀胱造瘘术。阴道镜检查显示双阴道,后阴道较大。 2岁时进行了后矢状肛门直肠穿刺成形术,并进行了1年的随访。尽管很少见,但在病毒性试验阴性且无心脏异常的胎儿腹水病例中,怀疑有泌尿生殖器异常。由于尿液通过试管完全排入腹膜,可能会缺少最常见的此类异常超声标记(充满液体的腔)。

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