bilateral congenital perineal hernias: spontaneous resolution
Clicks: 109
ID: 217303
2018
Article Quality & Performance Metrics
Overall Quality
Improving Quality
0.0
/100
Combines engagement data with AI-assessed academic quality
Reader Engagement
Steady Performance
30.0
/100
103 views
14 readers
Trending
AI Quality Assessment
Not analyzed
Abstract
A congenital perineal hernia develops through a defect in the pelvic floor muscles and presents as a reducible buttock swelling. These hernias are exceptionally rare with only six cases previously documented in the English literature. We report an extremely premature infant who developed bilateral posterior perineal hernias at 2 weeks of age. The diagnosis was confirmed by ultrasound scan. She remained asymptomatic. By a corrected age of 10 weeks post term, the hernias had resolved clinically and on imaging. A congenital perineal hernia should be considered in the differential diagnosis of a reducible buttock swelling. The diagnosis can be confirmed by imaging and elective surgical repair is indicated for symptomatic or persistent hernias. This case demonstrates that an asymptomatic perineal hernia in a very premature infant should initially be managed conservatively as it may resolve spontaneously. Keywords: Buttock mass, Pelvic hernia
| Reference Key |
harrison2018journalbilateral
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | ;Lachlan J.R. Harrison;Vaughan F. Richardson;Jean Murdoch;Mark D. Stringer |
| Journal | clinical medicine (london, england) |
| Year | 2018 |
| DOI |
DOI not found
|
| URL | |
| Keywords |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.