نتایج جستجو برای: diphallus

تعداد نتایج: 15  

2010
Ali-Reza Mirshemirani Naser Sadeghyian Leila Mohajerzadeh Hojat Molayee Parand Ghaffari

BACKGROUND Diphallus is an extremely rare anomaly. Numerous associated genitourinary, gastrointestinal and other anomalies have been described with diphallus. These patients need several investigations, and finally surgical intervention. CASES PRESENTATION In this report we discuss six patients with diphallus which evaluated retrospectively. Five patients had complete diphallia, and one had b...

2010
Alireza Mirshemirani Fatollah Roshanzamir Shahnaz Shayeghi Leily Mohajerzadeh Shaghayegh Hasas-yeganeh

BACKGROUND Diphallus is a rare anomaly and accompanying anomalies vary from bifid scrotum, bladder exstrophy, imperforate anus and colo-rectal anomaly such as duplication, and other associated anomalies. CASE PRESENTATION A 2-day old infant is reported with imperforate anus and complete duplication of recto-sigmoid colon, rectal pouch, doubling of the genitalia with completely formed penis (d...

Journal: :Proceedings of the Royal Society of Medicine 1930

Journal: :Proceedings of the Royal Society of Medicine 1968

2007
Abdulkadir Tepeler Mert Ali Karadağ Ünsal Özkuvancı Erhan Sarı Yalçın Berberoğlu Ahmet Yaser Müslümanoğlu

We herein present an unusual case of 14-year-old boy with complete diphallus and bifid scrotum. He was not aware of his extragenital abnormality until he was examined by a surgeon before circumsion. During surgery, the hypoplastic penis was resected and a single scrotum was constructed by removing the band of skin separating the compartments. The rugose skin was then joined, giving scrotal cont...

Journal: :medical journal of islamic republic of iran 0
abdollah nassehi from the department of urology, mashhad university of medical sciences, mashhad, islamic republic mohammad amir khammer

we report an unusual case of diphailus in a five year old boy. the two organs appeared separately, one orthotopically in the pubic area and the other in the perineum with no urinary meatus. a perineal hypospadias with meatus in the anterior anal verge was also present. the right testis was undescended and the scrotum was mildly bifid. the patient was continent for both voiding and defecation. m...

ABDOLLAH NASSEHI, MOHAMMAD AMIR KHAMMER,

We report an unusual case of diphaIlus in a five year old boy. The two organs appeared separately, one orthotopically in the pubic area and the other in the perineum with no urinary meatus. A perineal hypospadias with meatus in the anterior anal verge was also present. The right testis was undescended and the scrotum was mildly bifid. The patient was continent for both voiding and defeca...

2012
Mohamed Abdel Al M. Bakheet Mohammad Refaei

BACKGROUND Penile duplication (diphallus) is an extremely rare disorder. It is almost always associated with other malformations like double bladder, exstrophy of the cloacae, imperforate anus, duplication of the rectosigmoid and vertebral deformities. Meanwhile anal canal duplication, the most distal and least common duplication of the digestive tube and is a very rare congenital malformation....

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