Two Neonates with Congenital Hydrocolpos
Introduction. Neonatal hydrocolpos is a rare condition. Hydrocolpos is cystic dilatation of the vagina with fluid accumulation due to a combination of stimulation of secretary glands of the reproductive tract and vaginal obstruction. The differential for a neonatal presentation of lower abdominal ma...
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Format: | Article |
Language: | English |
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Wiley
2013-01-01
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Series: | Case Reports in Pediatrics |
Online Access: | http://dx.doi.org/10.1155/2013/692504 |
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author | Vydehi Murthy Jessica Costalez Julie Weiner Kristin Voos |
author_facet | Vydehi Murthy Jessica Costalez Julie Weiner Kristin Voos |
author_sort | Vydehi Murthy |
collection | DOAJ |
description | Introduction. Neonatal hydrocolpos is a rare condition. Hydrocolpos is cystic dilatation of the vagina with fluid accumulation due to a combination of stimulation of secretary glands of the reproductive tract and vaginal obstruction. The differential for a neonatal presentation of lower abdominal mass includes urogenital anomalies, Hirschsprung’s, disease or sacrococcygeal teratoma. Prenatal diagnosis and early newborn imaging studies leads to early detection and treatment of these cases. Case. We report here two cases of neonatal hydrocolpos with prenatal diagnosis of lower abdominal mass. Postnatally, ultrasound, MRI imaging, and cystoscopy confirmed large cystic mass as hydrocolpos with distal vaginal obstruction. Both patients had enlarged renal system secondary to mass effect. Conclusion. High index of suspicion for hydrocolpos in a newborn presenting with fetal diagnosis of infraumbilical abdominal mass will facilitate timely intervention and prevention of complications. |
format | Article |
id | doaj-art-7754a1e16c5a4b69b3f5d965416767f1 |
institution | Kabale University |
issn | 2090-6803 2090-6811 |
language | English |
publishDate | 2013-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Pediatrics |
spelling | doaj-art-7754a1e16c5a4b69b3f5d965416767f12025-02-03T01:09:47ZengWileyCase Reports in Pediatrics2090-68032090-68112013-01-01201310.1155/2013/692504692504Two Neonates with Congenital HydrocolposVydehi Murthy0Jessica Costalez1Julie Weiner2Kristin Voos3Children’s Mercy Hospital and Clinics, 2401 Gillham Road, Kansas City, MO 64108, USAChildren’s Mercy Hospital and Clinics, 2401 Gillham Road, Kansas City, MO 64108, USAChildren’s Mercy Hospital and Clinics, 2401 Gillham Road, Kansas City, MO 64108, USAChildren’s Mercy Hospital and Clinics, 2401 Gillham Road, Kansas City, MO 64108, USAIntroduction. Neonatal hydrocolpos is a rare condition. Hydrocolpos is cystic dilatation of the vagina with fluid accumulation due to a combination of stimulation of secretary glands of the reproductive tract and vaginal obstruction. The differential for a neonatal presentation of lower abdominal mass includes urogenital anomalies, Hirschsprung’s, disease or sacrococcygeal teratoma. Prenatal diagnosis and early newborn imaging studies leads to early detection and treatment of these cases. Case. We report here two cases of neonatal hydrocolpos with prenatal diagnosis of lower abdominal mass. Postnatally, ultrasound, MRI imaging, and cystoscopy confirmed large cystic mass as hydrocolpos with distal vaginal obstruction. Both patients had enlarged renal system secondary to mass effect. Conclusion. High index of suspicion for hydrocolpos in a newborn presenting with fetal diagnosis of infraumbilical abdominal mass will facilitate timely intervention and prevention of complications.http://dx.doi.org/10.1155/2013/692504 |
spellingShingle | Vydehi Murthy Jessica Costalez Julie Weiner Kristin Voos Two Neonates with Congenital Hydrocolpos Case Reports in Pediatrics |
title | Two Neonates with Congenital Hydrocolpos |
title_full | Two Neonates with Congenital Hydrocolpos |
title_fullStr | Two Neonates with Congenital Hydrocolpos |
title_full_unstemmed | Two Neonates with Congenital Hydrocolpos |
title_short | Two Neonates with Congenital Hydrocolpos |
title_sort | two neonates with congenital hydrocolpos |
url | http://dx.doi.org/10.1155/2013/692504 |
work_keys_str_mv | AT vydehimurthy twoneonateswithcongenitalhydrocolpos AT jessicacostalez twoneonateswithcongenitalhydrocolpos AT julieweiner twoneonateswithcongenitalhydrocolpos AT kristinvoos twoneonateswithcongenitalhydrocolpos |