ABSTRACT
Renal dysplasia results from aberrant metanephric histogenesis caused fundamentally by a defect in inducer tissue or responding tissue. Dysplastic kidneys vary tremendously in gross and microscopic appearance but are characterized by abnormal organization and a mixed population of primitive structures, such as fetal or immature cartilage, dysplastic ducts, immature tubules, and undifferentiated mesenchyme. We report a case of unilateral multicystic renal dysplasia associated with an ipsilateral ectopic ureteral orifice entering a seminal vesicle cyst in a 33-year-old man. He was admitted due to primary infertility which had developed three years ago. The his semen analysis revealed oligospermia. No evidence of a family history of renal dysplasia was reported. Microscopic examination showed that the entire kidney was composed of cysts lined by flattened cells, dysplastic ducts and immature tubules surrounded by collars of spindle cells, primitive mesenchyme, and a few aberrantly formed glomeruli.
Subject(s)
Adult , Humans , Male , Cartilage , Infertility , Kidney , Mesoderm , Multicystic Dysplastic Kidney , Oligospermia , Semen Analysis , Seminal Vesicles , UreterABSTRACT
Lumbar kidney is one of renal ectopia which rests opposite the sacral promontory in the iliac fossa and anterior to the iliac vessels. We have experienced a case of hypoplastic kidney associated with ipsilateral vaginal ectopic urethral opening which had been discovered by abdominal exploration.
Subject(s)
Kidney , UreterABSTRACT
An ectopic ureteral orifice inserts at a point other than the trigone of the bladder. Ectopic ureteral orifices in a girl commonly are associated with complete ureteral duplication comprises only 10 to 12 per cent of such patients. Continuous incontinence in a girl with an otherwise normal voiding pattern after toilet training is the classic sign of an ectopic ureteral orifice. Here, we report a 3-years-old girl who was admitted to our hospital due to continuous urinary incontinence and managed with the diagnosis of bilateral ectopic ureteral orifices associated with bilateral complete ureteral duplication.
Subject(s)
Female , Humans , Diagnosis , Toilet Training , Ureter , Urinary Bladder , Urinary IncontinenceABSTRACT
A case of unilateral multicystic renal dysplasia was reported in view of rarity, and a review of literature 23-year-old female was admitted to Kyung Hee University Hospital with a complaint of urinary incontinence. An excretory urogram revealed non-visualization of the right kidney. The right ureter had opening at the 2 cm above the vaginal introitus. The resected right kidney revelaed multilobulated outer surface with multiloculated cystic struture on cut surface. The associated anomaly was uterine didelphy. The condition was treated by nephroureterectomy.
Subject(s)
Female , HumansABSTRACT
A case of unilateral multicystic renal dysplasia was reported in view of rarity, and a review of literature 23-year-old female was admitted to Kyung Hee University Hospital with a complaint of urinary incontinence. An excretory urogram revealed non-visualization of the right kidney. The right ureter had opening at the 2 cm above the vaginal introitus. The resected right kidney revelaed multilobulated outer surface with multiloculated cystic struture on cut surface. The associated anomaly was uterine didelphy. The condition was treated by nephroureterectomy.
Subject(s)
Female , HumansABSTRACT
The ectopic ureteral orifice is commonly associated with duplicated ureter But it is relatively rare that duplicated ureter has ectopic ureteral orifices in company. Herein, in 2 year old girl, we report a case of ectopic ureteral orifices in unilateral duplicated ureter which are located in bladder neck, distal urethra. She has been suffered from continual dribbling despite normal pattern of voiding, treated with ureteral reimplantation in common sheath.
Subject(s)
Child, Preschool , Female , Humans , Neck , Replantation , Ureter , Urethra , Urinary BladderABSTRACT
We present a case of left ectopic ureteral orifice to the vagina with a hypoplastic kidney in a 15 year old girl and a case of ectopic ureteral orifice to the vaginal vestibule associated with bilateral complete double ureter in a 5 year old girl. They presented with urinary incontinence while normally secured voluntary voiding. Fifteen year old girl was treated with left nephrectomy and the other girl with heminephrectomy.
Subject(s)
Adolescent , Child, Preschool , Female , Humans , Kidney , Nephrectomy , Ureter , Urinary Incontinence , VaginaABSTRACT
We herein presented a case of left ectopic ureteral orifice to the vagina in a 14 year old girl containing stones in the distal ectopic ureteral portion of associated complete duplicated ureter. She has been suffered from urinary leakage while normal voiding since birth without other urinary symptoms. She was treated with left ureteroneocystostomy.
Subject(s)
Adolescent , Female , Humans , Parturition , Ureter , VaginaABSTRACT
The renal agenesis and ectopic ureter were relatively rare congenital disease, but their combined form was more extremely rare condition. We report a case of ectopic ureteral opening associated with ipsilateral renal agenesisthat noted recurrent epididymitis in 18 month old children with review of literatures.
Subject(s)
Child , Humans , Infant , Male , Epididymitis , UreterABSTRACT
One case of right duplicated ureter associated with single ectopic ureteral orifice to the vaginal vestibule in a 14-year old girl was presented. In a case, while normal self-voiding, urinary leakage has been complained since infant without other urinary symptoms and she was treated with right ureteronecystostomy in Paquin's method.
Subject(s)
Adolescent , Female , Humans , Infant , UreterABSTRACT
One case of right duplicated ureter associated with single ectopic ureteral orifice to the vaginal vestibule in a 23 year old girl was presented. In a case, while normal self-voiding, urinary leakage has been complained since infant without other urinary symptoms and she was treated with right ureteroheminephrectomy.