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Information Journal Paper

Title

POSTERIOR URETHRAL POLYP: A RARE CASE

Pages

  203-207

Abstract

 Urethral POLYPS are a rare finding in CHILDren. Urethral fibro epithelial POLYPS are usually discovered in the first decade of life. They present with voiding dysfunction, obstructive and irritative urinary symptoms, and hematuria. They may be associated with other congenital urinary tract anomalies. Histopathologically, they are usually benign lesions with no tendency to recurrence and are treated by surgical ablation, fulguration or laser therapy. Diagnosis is made by sonography, voiding cystourethogram and cystoscopy. In this report, a rare case of posterior urethral polyp in an eight –year old male CHILD is presented.

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    APA: Copy

    KAMALATI, A., & NEMATOLLAHI, N.. (2013). POSTERIOR URETHRAL POLYP: A RARE CASE. JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES, 20(2), 203-207. SID. https://sid.ir/paper/321/en

    Vancouver: Copy

    KAMALATI A., NEMATOLLAHI N.. POSTERIOR URETHRAL POLYP: A RARE CASE. JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2013;20(2):203-207. Available from: https://sid.ir/paper/321/en

    IEEE: Copy

    A. KAMALATI, and N. NEMATOLLAHI, “POSTERIOR URETHRAL POLYP: A RARE CASE,” JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES, vol. 20, no. 2, pp. 203–207, 2013, [Online]. Available: https://sid.ir/paper/321/en

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