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http://dx.doi.org/10.1007/s12519-010-0014-5DOI Listing

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Article Synopsis
  • Acquired urethral diverticula (UD) in males is an unusual condition, often occurring post surgeries like prostatectomy, and this case highlights its occurrence after holmium laser enucleation of the prostate (HoLEP) in a 69-year-old man.
  • The patient had a significantly enlarged prostate and experienced multiple episodes of urine retention and infections, despite medical treatment; he was ultimately diagnosed with a 6-cm UD following urodynamics, cystoscopy, and imaging tests.
  • After surgical intervention to remove the diverticulum, the patient still faced challenges with mixed urine incontinence, suggesting that UD may be a rare but important consideration in men with recurrent urinary tract infections and incontinence following prostate surgery.
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Prolonged ischemic priapism presents a treatment challenge given the difficulty in achieving detumescence and effects on sexual function. To evaluate current practice patterns, an open, web-based multi-institutional survey querying surgeons' experience with and perceived efficacy of tunneling maneuvers (corporoglanular tunneling and penoscrotal decompression), as well as impressions of erectile recovery, was administered to members of societies specializing in male genital surgery. Following distribution, 141 responses were received.

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A Boy with 46,XX Karyotype (SRY double-positive) having a Leydig Cell Tumor.

J Clin Res Pediatr Endocrinol

March 2023

Department of Pediatric Endocrinology, University of Health Science, Antalya Training and Research Hospital, Antalya, Turkey.

Leydig cell tumors are the most common type of testicular sex cord stromal tumors. Presence of Y chromosome is associated with tumor risk in sex development disorder (DSD), however tumor development without Y chromosome are extremely rare. A 16-year-old boy diagnosed with Leydig cell tumor due to a mass in the right testis was referred after the right orchiectomy.

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Ectopic scrotum and penoscrotal transposition: Case report and literature review.

Front Pediatr

February 2023

Department of Pediatric Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Background: Ectopic scrotum (ES) is an extremely rare congenital scrotal malformation. Ectopic scrotum with VATER/VACTERL [vertebral defects (V), anal atresia or anorectal malformations (A), cardiac defects (C), tracheoesophageal fistula with or without esophageal atresia (TE), cardiac defects, renal malformations (R), and limb defects (L)] association is even rarer. There are no uniform guidelines for diagnosis and treatment.

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