Results 11 to 20 of about 1,510 (167)

Modified Cantwel-Ransley Reconstruction of Continent Penile Epispadias In Children: A Case Report

open access: yesFolia Medica Indonesiana, 2021
Epispadias as an isolated embryologic defect is a rare anomaly, with an incidence of 1 in 117.000 males. Isolated epispadias with continence is a very rare condition comprising less than 10% of all epispadias cases.
Ahmad Nadhir, Tarmono Tarmono
doaj   +8 more sources

Female epispadias

open access: yesAfrican Journal of Paediatric Surgery, 2011
Isolated female epispadias without bladder exstrophy is an extremely rare congenital anomaly. The symptoms of female epispadias are primary urinary incontinence and abnormal anatomical features.
M V Krishna Shetty, A Bhaskaran, T K Sen
doaj   +4 more sources

Delayed Presentation of Classic Bladder Exstrophy Associated With Epispadias and Bilateral Non‐Scrotal Testes in an 11‐Year‐Old Afghan Boy: A Case Report

open access: yesClinical Case Reports
Bladder exstrophy–epispadias complex (BEEC) is a rare congenital anomaly due to failure of lower abdominal wall and urinary tract closure. We report an 11‐year‐old boy with neglected bladder exstrophy, epispadias, and bilateral cryptorchidism.
Abdul Ghafar Ghayur   +5 more
doaj   +2 more sources

Urothelial carcinoma occurring in a defunctionalized bladder after urinary diversion due to the bladder exstrophy‐epispadias complex

open access: yesIJU Case Reports
Introduction The bladder exstrophy‐epispadias complex is a rare congenital disease. Urothelial carcinomas rarely occur in patients with this disease, and there have been few reports on its treatment.
Toshiharu Morikawa   +8 more
doaj   +2 more sources

Cantwell-Ransley technique in complete epispadias repair [PDF]

open access: yesAin-Shams Journal of Surgery, 2014
Background/Purpose: Epispadias  is a rare congenital  anomaly of the external genitalia occurring in approximately one in 118 000 males and one in 400 000 females.
Mohamed Hashish   +3 more
doaj   +1 more source

Technical details in the primary repair of male epispadias: Step by step video

open access: yesUrology Video Journal, 2022
Objective: the primary correction of male epispadias consists of multiple surgical steps: isolation of the complex corpora-urethral plate, bladder neck plasty if incontinence is associated, tubularization of the urethral plate, correction of dorsal ...
JL Pippi Salle   +6 more
doaj   +1 more source

Complete female epispadias with urinary incontinence: A single-stage perineal urethroplasty and cystoscopic-guided bladder neck plication

open access: yesAfrican Journal of Paediatric Surgery, 2023
Isolated female epispadias without bladder exstrophy is an extremely rare congenital anomaly. The presenting features of female epispadias are urinary incontinence and abnormal anatomical features.
Rajat Piplani, Enono Yhoshu
doaj   +1 more source

Single-Stage Trans-Vestibular and Foley’s-Assisted Epispadias Repair (STAFER) for Girls with Incontinent Epispadias: A Retrospective Study from a Tertiary-Care Center

open access: yesUro, 2022
Objective: The aim of this study was to evaluate the outcomes of single-stage trans-vestibular and Foley’s assisted epispadias repair (STAFER) technique in girls with incontinent epispadias.
Minu Bajpai, Sachit Anand, Prabudh Goel
doaj   +1 more source

Management of the exstrophy-epispadias complex in adolescents and adults

open access: yesAfrican Journal of Urology, 2017
Objectives: To study the presentation and management of the exstrophy-epispadias complex in adolescents and adults and to evaluate the outcome of the repair. Subjects and methods: This retrospective review of our medical records of adult patients with an
A. Jana   +3 more
doaj   +1 more source

Exstrophy-Epispadias Complex Variants: A Hybrid Case

open access: yesPediatric Reports, 2021
The term exstrophy-epispadias complex refers to a group of midline defects ranging from epispadias to cloacal exstrophy. Bladder exstrophy is the most frequent malformation of this spectrum and it can present as a classical or a variant form. We report a
Alba Ganarin   +5 more
doaj   +1 more source

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