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Parameatal cyst of urethra: a rare congenital anomaly

Metin Onaran1, Mustafa Ozgür Tan, Ahmet Camtosun

  • 1School of Medicine, Urology Department, Gazi University, 12. kat, 06510, Besevler, Ankara, Turkey. monaran@gazi.edu.tr

International Urology and Nephrology
|July 27, 2006
PubMed

Insights

A rare congenital anomaly, parameatal urethral cyst, was observed in a 15-year-old boy. Complete surgical excision of the cyst and its epithelium is crucial for effective treatment and preventing recurrence.

Area of Science:

  • Urology
  • Pediatric Surgery
  • Congenital Anomalies

Background:

  • Parameatal urethral cysts are rare congenital anomalies of the male urethra.
  • Early recognition and management are often limited, with delayed presentation common.

Observation:

  • A 15-year-old male presented with a parameatal urethral cyst, initially identified in infancy.
  • The cyst had enlarged significantly, causing urinary spraying and cosmetic concerns.

Findings:

  • The case highlights a delayed presentation of a parameatal urethral cyst.
  • Surgical intervention is necessary for symptomatic relief and improved quality of life.

Implications:

  • Complete excision of the cyst, including its epithelial lining, is essential for preventing recurrence.
  • This case underscores the importance of timely diagnosis and surgical management of rare urethral anomalies in pediatric patients.

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