congenital urethral polyp in a preterm neonate

Clicks: 120
ID: 202844
2018
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Ranked #57 of 72 articles by views in clinical medicine (london, england)

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Abstract
A congenital urethral polyp is a benign soft tissue lesion that rarely manifests in young males presenting with lower urinary tract symptoms [1]. Until 2004 there were only 181 reported cases with an age range from 21 days to 90 years [2]. In February 2017 only the fifth neonatal case was reported [3]. The occurrence in neonates from birth is extremely uncommon and more so in a preterm infant, hence this publication [2,5]. When suspected, the diagnosis is usually confirmed on micturition cystourethrogram, ultrasound or cystoscopy [1]. The following case study will explore the presentation of fibro-epithelial polyp on a preterm male newborn presenting with a visible transurethral mass, which was successfully excised.
Reference Key
morare2018journalcongenital Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Nolitha T. Morare;Thomas Rangaka;Ricardo Gonzales
Journal clinical medicine (london, england)
Year 2018
DOI
10.1016/j.epsc.2017.10.010
URL
Keywords Keywords not found

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