1.5 cases of the Cryptorchidism Treated with Hormonal Therapy (H.C.G.).
Korean Journal of Urology 1982;23(1):109-112
5 cases of cryptorchidisms were treated with H.C.G. during the period from Feb. 1980 to Sept. 1980. Among them, in 3 cases of bilateral cryptorchidism, H.C.G. effect was surprisingly excellent in doses of 5,500 I.U. of puberogen for 7 weeks, 6,000 I.U. for 4 weeks and 4,000 I.U. for 4 weeks respectively. In 2 cases of unilateral cryptorchidisms the H.C.G. effect was rather unsuccessful, but seemed to be meaningful. H.C.G. treatment was thought to be valuable prior to surgery especially in bilateral cryptorchidism.
Cryptorchidism*
;
Male
2.Hormonal Therapy on Cryptorchidism.
Korean Journal of Urology 1971;12(1):51-57
No abstract available.
Cryptorchidism*
;
Male
3.The Incidence of Undescended Testes at Birth.
Chong Koo CHONG ; Wan Chol SO ; Byong Lyol LEE ; E Boong KWON ; Sung Il AHN
Journal of the Korean Pediatric Society 1984;27(7):673-677
No abstract available.
Cryptorchidism*
;
Incidence*
;
Male
;
Parturition*
4.A case of Torsion of the Undescended Testis in the Infant.
Jin Su PARK ; Hyung Chul PARK ; Sang Hun BAEK ; Jin Kyu LIM ; Jung Seog HWA ; Ky Hyun CHUNG
Korean Journal of Urology 2000;41(4):569-571
No abstract available.
Cryptorchidism*
;
Humans
;
Infant*
;
Male
5.Surgical treatment of undescended testis by elongating the spermatic vessel and cord
Journal of Vietnamese Medicine 1998;231(12):113-119
In the Urological Department of Cho Ray hospital 1n 1998, 10 cases with non-palpable testis were operated. The lowest age of patients was 6 years old, the highest age was 27, the average was 14. Eight testes were in iliac fossae, 2 testes were in internal inguinal ring. Authors used technique liberating testicular vessels: elongating spermatic vessel and cord long enough to allow the testis to be placed into scrotum; creating a direct path to scrotum and thus, it is able to descend the testis into the scrotum by single stage orchidopexy, without traction on the vessels and damaging the blood supplying for testis. Six of ten cases were followed-up after operation by Doppler Ultrasonography. All receive good blood supply, no atrophy of testis was seen after operation
Cryptorchidism
;
Spermatic Cord
;
surgery
6.Analysis of cytogenetic nature in 21 children with undescended testes
Journal of Practical Medicine 2005;503(2):29-31
Study on 21 children with bilaterally or unilaterally undescended testes at Vietnam National hospital of Pediatrics. These children were from 6 months to 15 years old, 90,5% of them was ≥ 3 years old. There wasn’t any disorder in quantity and structure of chromosome in all patients. They were analysed Barr bodies and results were nagative. The results were correspond to karyotyp 46, XY All patients had coresponding in clinical diagnosis and cytogenetic test diagnosis
Cryptorchidism
;
Cytogenetics
;
Child
7.Epididymal Abnormalities and the Patency of Processus Vaginalis Associated with Hydrocele/hernia and Undescended Testis.
Beom Jun PARK ; Deok Yun KIM ; Jae Shin PARK
Korean Journal of Urology 1995;36(6):623-628
Epididymal abnormalities have long been found in conjunction with undescended testis. Undescended testis with a patent processus vaginalis are associated with epididymal abnormalities, but the incidence of epididymal abnormalities in descended testis with a patent processus has not been reported. We analyzed the patency of processus vaginalis and epididymal abnormalities of 37 patients(41 testes) treated for undescended testes and 78 patients(79 testes) treated for hydrocele. Epididymal abnormalities ranged from simple epididymal elongation, epididymal angulation, disruption between testis and epididymal tail to more complex forms, such as epididymal/vasal atresia, complete disruption between the testis and epididymal head. Among 38 undescended testis with patent processus vaginalis 27(71%) had an epididymal abnormalities compared to 12 of 37(32%)hydroceles with patent processus vaginalis(P<0,05), and 12 of 38(329b) undescended testis with patent processus vaginalis had complex epididymal abnormalities(epididymal head separation and epididymal atresia) compared to 2 of 37(5%) hydroceles with patent processus vaginalis (p<0.05). Among 37 hydroceles with patent processus vaginalis 12(32%) had an epididymal abnormalities compared to 2 of 37(5%) hydroceles with incompletely patent processus vaginalis(P<0.05). These data suggest that epididymal abnormalities probably contribute to both testicular maldescent and closure of processus vaginalis.
Cryptorchidism*
;
Head
;
Incidence
;
Male
;
Testis
8.HCG therapy for extracanalicularly located testis.
Korean Journal of Urology 1992;33(3):468-471
Reported results of HCG treatment for cryptorchism are quite variable because many factors may influence the success of the therapy. It is possible that the anatomic stratification introduces an element of selection bias into the data. 12 cases of extracanalicularly located testis were treated with HCG from December 1988 year to June 1990 year. Five of the 12 cases were cosmetically satisfactory. 3 became retractile testis which is disturbing in all that could be treated successfully but could not be satisfactory from the cosmetic point of view. Apparent hernial sac developed in 4 cases who were clinically inapparent before initiation of the hormonal therapy.
Cryptorchidism
;
Male
;
Selection Bias
;
Testis*
9.Clinical Observations on 48 Cases of Hypospadias.
Korean Journal of Urology 1977;18(2):167-172
A clinical observation was made on 48 hypospadias of the in-patients in the Department of Urology, Yonsei University Hospital during the period Jan. 1966 through Dec. 1975 and the following results were obtained. 1) Of 48 hypospadias, 29 cases(60.2%) were admitted at the age of 7 or below and 19 cases(39.8%) at the ages of 8 years or more. 2) Of 48 hypospadias, 29 cases(79.2%) were peno-scrotal, 8 cases(16.6%) penile and 2 cases(4.2%) were perineal in type. 3) Cryptorchism was the most common associated anomaly and it occupied 23.3% of 30 associated anomalies. 4) Of 33 urethroplasties, 12 cases(63.1%) were succeed by Thiersch-Duplay method and 12 cases(85.7%) were succeed by Ikoma's method.
Cryptorchidism
;
Female
;
Hypospadias*
;
Male
;
Urology
10.A Case of Rt. Renal Agenesis Combined with Cryptorchism and Neuroblastoma.
Hee Jung CHUNG ; Chul LEE ; Pyung Kill KIM ; Chang Jin KIM ; Kwang Kill LEE ; Yu Bok LEE ; Ki Keun OH
Journal of the Korean Pediatric Society 1981;24(7):677-684
Congenital unilateral renal agenesis is a rare congenital anomaly. Furthermore, renal agenesis associated with neuroblastoma and cryptorchism is more rare in incidence. Recently we experieced a case of Rt. renal agenesis combined with cryptorchism and neuroblastoma. We diagnosed it with IVP and selective renal angiography and confirmed it with explolaparotomy and biopsy. We reviewed the literatures on renal agenesis, cryptorchism and neuroblastoma, and discussed possible embryological relationships between them and other combined congenital anomalies.
Angiography
;
Biopsy
;
Cryptorchidism*
;
Embryology
;
Incidence
;
Male
;
Neuroblastoma*