2018
DOI: 10.1155/2018/1425953
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Congenital Uterovaginal Prolapse in a Newborn

Abstract: Background Uterovaginal prolapse is a rare condition in newborns which is usually associated with spinal cord defects. It is usually diagnosed at birth. Different treatment options have been proposed for genital prolapse in newborns. Most of the treatment options recommended are conservative; radical approach is rarely suggested for the treatment of these cases. Case Details We report a 6-hour-old newborn that was diagnosed to have congenital uterovaginal prolapse and was successfully managed conservatively wi… Show more

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Cited by 6 publications
(8 citation statements)
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“…The management of these "congenital hydrocephalic paraplegics" is complex, multidisciplinary and long-term [5] [6] [7]. There is a need for regular follow-up in neurosurgery [5], orthopaedics and urology, and for rehabilitation sessions [1] [8].…”
Section: Discussionmentioning
confidence: 99%
“…The management of these "congenital hydrocephalic paraplegics" is complex, multidisciplinary and long-term [5] [6] [7]. There is a need for regular follow-up in neurosurgery [5], orthopaedics and urology, and for rehabilitation sessions [1] [8].…”
Section: Discussionmentioning
confidence: 99%
“…Uterine prolapse is a therapeutic emergency to prevent complications. Such as urinary obstruction, which can lead to hydronephrosis, or endometrial metaplasia [6] [7]. No consensus management protocol has been established.…”
Section: Discussionmentioning
confidence: 99%
“…It ranges from conservative treatment to surgical treatment. Manual reduction under anaesthesia has been strongly reported [1] [6]. This reduction is held in place either by an intravaginal wick with a compression bandage for 72 hours on average [6].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Uterovaginal prolapse is defined as the descent and protrusion of the uterus and vagina outward through the vaginal opening [1] [2]. It is a rare condition in newborns [3] [4] [5] [6]; diagnosis is usually made at birth or in the first few days of life [4] [7]. It is most often associated with neural tube closure anomalies, in particular myelomeningocele and spina bifida occulta [2] [3] [5].…”
Section: Introductionmentioning
confidence: 99%