PSEUDODIPHALLIA WITH DUPLICATION OF URETHRA. Pseudodifalia con duplicación de uretra
نویسندگان
چکیده
منابع مشابه
Urethra duplication with bladder outlet membrane obstruction
A two-year-old boy presented with voiding through two orifices, with one greater than the other. On physical examination, he had bifid glans penis with a complete foreskin and no other anomaly (Figure 1). The urinalysis and urine culture were normal. It is difficult to find the internal opening of the urethra by cystoscopy through cystostomy. Catheterization through the external openings of the...
متن کامل[Sertoli cell tumor of the testis with positive neuroendocrine markers].
de los pacientes se diagnostican en los primeros años de vida. La forma de presentación clı́nica más frecuente es la existencia de un doble meato uretral y/o un doble chorro miccional. Otras manifestaciones descritas son la presencia de infecciones urinarias de repetición, reflujo vesicoureteral, incontinencia y goteo perineal durante la micción. El diagnóstico se basa en la exploración fı́sica c...
متن کاملComplete duplication of urinary bladder and urethra: prenatal sonographic features.
Prenatal sonographic features of the rare anomaly of complete duplication of the urinary bladder and urethra are described in this case report. A coronal scan of the fetal pelvis at 29 weeks of gestation revealed two pyriform cystic structures. The umbilical arteries coursed around both of them. They emptied independently of each other. Postnatally the newborn had two vulvae, two anal openings,...
متن کاملComplete duplication of bladder and urethra: a case report.
A case of complete duplication of the bladder and urethra in a girl is reported, demonstrating outlet obstruction in the bladder on the left side. Associated anomalies and pertinent literature are reviewed.
متن کاملFirst Case of Complete Bladder Duplication in the Coronal Plane with Concomitant Duplication of the Urethra in an Adult Male
Duplication of the lower urinary tract is a very rare congenital anomaly which is diagnosed either at birth or during early childhood. These rare malformations are most of the times accompanied by other concomitant anomalies and are therefore diagnosed immediately after birth. In some even rarer cases there are no concomitant anomalies and symptoms thus leading to a diagnosis later in childhood...
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ژورنال
عنوان ژورنال: Revista Argentina de Anatomía Clínica
سال: 2016
ISSN: 1852-8023
DOI: 10.31051/1852.8023.v4.n1.13946