Literature DB >> 9120985

The genetic male with absent penis and urethrorectal communication: experience with 5 patients.

W H Hendren1.   

Abstract

PURPOSE: Congenital aphallia is a rare anomaly that occurs only once in 30 million births. Five cases are described.
MATERIALS AND METHODS: All 5 patients 4 to 20 years old had been reared as female. The bladder neck or short urethra entered the anterior rectum in each patient. At referral 2 patients had a vesicostomy and 1 had a colostomy. Hydronephrosis and vesicoureteral reflux were present in 2 and 3 cases, respectively. After separating the urinary tract from the rectum a urethra was created in each patient and a bowel vagina was constructed in 4 during the same operation. The initial patient did not undergo simultaneous creation of a vagina.
RESULTS: One patient later required a bladder neck narrowing operation for stress incontinence. She became incontinent again after transpubic surgery to create a sigmoid vagina was performed elsewhere 8 years later. The other 4 patients are dry, and they have normal urinary and bowel control.
CONCLUSIONS: A single extensive operation on the bladder, vagina and rectum simultaneously is the ideal approach in these cases using the prone posterior sagittal and supine abdominal perineal positions.

Entities:  

Mesh:

Year:  1997        PMID: 9120985

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  6 in total

1.  Discordant sexual identity in some genetic males with cloacal exstrophy assigned to female sex at birth.

Authors:  William G Reiner; John P Gearhart
Journal:  N Engl J Med       Date:  2004-01-22       Impact factor: 91.245

Review 2.  Male gender assignment in aphallia: a case report and review of the literature.

Authors:  Percy Jal Chibber; Hemendra N Shah; Pritesh Jain; Prabha Yadav
Journal:  Int Urol Nephrol       Date:  2005       Impact factor: 2.370

Review 3.  Aphallia: a review to standardize management.

Authors:  Tarryn Gabler; Robyn Charlton; Jerome Loveland; Ellen Mapunda
Journal:  Pediatr Surg Int       Date:  2018-04-20       Impact factor: 1.827

4.  Congenital aphallia associated with congenital urethrorectal fistula: A rare case report.

Authors:  Si-Si Luo; Zhe Yang; Ning Ma; Wei-Xin Wang; Sen Chen; Qi Wu; Si-Wei Qu; Yang-Qun Li
Journal:  Medicine (Baltimore)       Date:  2022-02-18       Impact factor: 1.817

5.  A rare case of penis agenesis (Aphallia) with associated multiple urogenital anomalies.

Authors:  Zafer Demirer; Bilal Firat Aip; Sami Uguz; Ali Guragac; Hasan Cem Irkilata
Journal:  Int J Surg Case Rep       Date:  2015-08-10

6.  A case report of aphallia with urorectal septum malformation sequence in a newborn: a very rarely seen condition.

Authors:  Deepak Sharma; Ravinder Singh; Sweta Shastri
Journal:  Int Med Case Rep J       Date:  2015-12-04
  6 in total

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