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      Large, infected Cowper’s syringoceles: a rare cause of perineal sepsis in adult men

      case-report
      , ,
      Journal of Surgical Case Reports
      Oxford University Press

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          Abstract

          Urologists and general surgeons alike are familiar with assessing acute perineal pathology. A Cowper’s gland syringocele is a rare cystic dilatation of the male bulbourethral gland, typically seen in children. We report the diagnosis and emergency management of two adult cases of large, infected Cowper’s gland syringoceles. A comorbid 76-year old was diagnosed with sepsis and penile swelling, but there was no discrete superficial pathology. Magnetic resonance imaging (MRI) revealed a perineal collection communicating with the membranous urethra. A suprapubic catheter was inserted, and aspiration was attempted. Meanwhile, a 55-year-old diabetic presented with severe perineal pain. MRI revealed a deep perineal collection, involving the scrotum and proximal penis. He improved with antibiotics and aspiration of the collection. This rare diagnosis may be more common in older men than previously thought. Pelvic MRI is a key diagnostic tool. A minimally invasive approach is possible in those with considerable perioperative risk.

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          Invasive Streptococcus anginosus group infection-does the species predict the outcome?

          To determine whether there is an association between the species of Streptococcus anginosus group (SAG) bacteria and the clinical outcome.
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            Cowper's syringocele: symptoms, classification and treatment of an unappreciated problem.

            Cowper's syringocele is a rare deformity in the male urethra that is a distention of the duct of the bulbourethral (Cowper's) gland. We report on 7 cases, review the symptoms and pathophysiology, and propose a simplified classification of this uncommon lesion. We reviewed 7 cases of Cowper's syringocele diagnosed from 1997 to 1998 at our hospital. Cowper's syringocele was diagnosed in 7 patients 25 to 51 years old with persistent post-void dribbling, frequency, urethral pain, hematuria or sudden urethral discharge. Diagnosis was made with urethrocystoscopy or retrograde urethrogram. Cowper's syringocele may be closed (a distended cyst-like swelling in the wall of the urethra) or open (an opening enabling urine reflux into the syringocele). In 2 patients asymptomatic open syringocele was diagnosed. In 1 patient symptomatic syringocele resolved spontaneously following an infection. In 4 patients open syringocele was treated with transurethral marsupialization because of persistent post-void dribbling. Postoperatively patients were completely symptom-free with a mean followup of 12 months (range 6 to 23). Cowper's syringocele may be more common than currently realized. Urologists should rule out this possibility in young male patients with lower urinary tract symptoms and persistent post-void dribbling as it can be treated easily.
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              A neglected gland: a review of Cowper's gland

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                Author and article information

                Contributors
                Journal
                J Surg Case Rep
                J Surg Case Rep
                jscr
                Journal of Surgical Case Reports
                Oxford University Press
                2042-8812
                December 2022
                07 December 2022
                07 December 2022
                : 2022
                : 12
                : rjac568
                Affiliations
                Department of Urology, Whipps Cross University Hospital , London E11 1NR, UK
                Department of Radiology, Whipps Cross University Hospital , London E11 1NR, UK
                Department of Urology, Whipps Cross University Hospital , London E11 1NR, UK
                Author notes
                Correspondence address. Department of Urology, Whipps Cross University Hospital, Barts Health NHS Trust, London E11 1NR, UK. E-mail: k.o.adasonla@ 123456doctors.org.uk
                Author information
                https://orcid.org/0000-0002-2673-4390
                Article
                rjac568
                10.1093/jscr/rjac568
                9731618
                36518654
                8be33ad3-ff8b-47bb-b32e-476e0c9dbfdd
                Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2022.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 29 October 2022
                : 19 November 2022
                Page count
                Pages: 4
                Categories
                AcademicSubjects/MED00910
                jscrep/0170
                Case Series

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