MEGALOURETHRA: A CASE REPORT

Abstract

Congenital megalourethra is a rare mesenchymal anamoly of the male urethra. It is defined as dilation of the anterior urethra due to absence of development or deficiency of erectile tissue of the penis. It leads to deformity of the penis (scaphoid megalourethra) or impotence (fusiform megalourethra) and also renal insufficiency and pulmonary hypoplasia. The associated anomalies are often life threatening and influence the management and prognosis. We present here a report of a case of megalourethra.

Authors and Affiliations

Aditya Pratap Singh| M.ch. (Resident), Department of Pediatric surgery, S.M.S. Medical College, Jaipur, Corresponding author email: dr.adisms@gmail.com, Javed Salam Ansari| M.ch. (Resident), Department of Pediatric surgery, S.M.S. Medical College, Jaipur, Arvind Shukla| Professor Department of Pediatric surgery, S.M.S. Medical College, Jaipur, Aadil Farooq| M.ch. (Resident), Department of Pediatric surgery, S.M.S. Medical College, Jaipur, Veenita Chaturvedi| Professor Department of Pediatric surgery, S.M.S. Medical College, Jaipur, Morya DP| M.ch. (Resident), Department of Pediatric surgery, S.M.S. Medical College, Jaipur

Keywords

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  • EP ID EP11285
  • DOI 10.5958/2319-5886.2014.00050.2
  • Views 269
  • Downloads 13

How To Cite

Aditya Pratap Singh, Javed Salam Ansari, Arvind Shukla, Aadil Farooq, Veenita Chaturvedi, Morya DP (2014). MEGALOURETHRA: A CASE REPORT. International Journal of Medical Research & Health Sciences (IJMRHS), 3(4), 1044-1046. https://europub.co.uk./articles/-A-11285