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A case of Herlyn-Werner-Wunderlich syndrome: a rare, congenital genitourinary anomaly in a 12-year-old girl

Park JW, Jung JY

Herlyn-Werner-Wunderlich (HWW) syndrome is a rare, congenital genitourinary anomaly involving the Müllerian and Wolffian structures, and is characterized by the triad of uterine didelphys, obstructed hemivagina, and ipsilateral renal agenesis....
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A female adnexal tumor of probable Wolffian origin showing positive O-6-methylguanine-DNA methyltransferase methylation

Kwon MJ, Yun MJ, Kim MK

Female adnexal tumor of probable Wolffian origin (FATWO) is a rare disease entity that arises from the mesonephric duct system. FATWO is different than other gynecological cancers in terms of...
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Ectopic Epididymis in Testicular Appendices: Report of Two Cases

Kim HS, Kim GY, Lee HL, Kim YW, Lim SJ

We report two cases of ectopic epididymal ducts and efferent ductules in the testicular appendices (TAs) of adult men with normally descended testes. In both cases, a sessile TA was...
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A Case Of Mullerian Cyst Of Vulva

Oh IY, Lim MC, Lee JH, Huh CY, Kim SB

  • KMID: 1925527
  • Korean J Obstet Gynecol.
  • 2002 Aug;45(8):1393-1395.
The pathogenesis and origin of vulvar cyst lined by a ciliated columnar epithelium is unknown. But it is suggested that origins of the epithelium of cyst are Mullerian or Wolffian...
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An Experience of Vaginoplasty with Rectos Abdominis Myocutaneous Flap for Testicular Feminization Syndrome

Park SY, Lee JK, Jeon SH, Lee JO, Seong IG, Han BH

  • KMID: 2290287
  • Korean J Urol.
  • 1998 Dec;39(12):1270-1273.
Testicular feminization syndrome is characterized by 46,XY karyotype, bilateral testes, absent or hypoplastic wolffian duct, female appearing external genitalia, blind vaginal pouch, and absent or rudimentary muillerian derivatives. We experienced...
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A Case Report of Complete Androgen Insensitivity Syndrome

Kim SY, Hwang KJ, Ahn HS, Joo HJ, Joo YJ, Kwon HC, Oh KS

  • KMID: 2269628
  • Korean J Obstet Gynecol.
  • 1999 May;42(5):1146-1150.
The androgen insensitivity syndrome is a heterogeneous disorder with a wide spectrum of phenotypic abnormalities, ranging from complete female to ambiguous forms that more closely resembles males. Mutations...
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Two Cases of Herlyn-Werner-Wunderlich Syndrome Diagnosed in Perinatal Period

Ahn JH, Shin SH, Lee J, Sohn JA, Lee JA, Choi CW, Kim EK, Kim HS, Kim BI, Choi JH

Herlyn-Werner-Wunderlich syndrome (HWWS) is a very rare congenital anomaly of the urogenital tract involving Mullerian ducts and Wolffian ducts, and is characterized by the triad of uterine didelphys, unilateral obstructed...
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Sonographic Findings of the Uterus Didelphys associated with Obstructed Hemivagina and Ipsilateral Renal Agenesis: Report of 4 Cases

Kim JH, Lee HK, Choi DS, Lee SW, Bae CS, Yoon HW, Kim MW, Kim SJ

  • KMID: 1614846
  • J Korean Soc Med Ultrasound.
  • 2001 Sep;20(3):201-206.
The association of uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis is rare anomaly. It is caused by failure in the fusion of the caudal portion of the M...
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A Case of Posterior Urethral Valve

Choi YS, Park JY, Ahn DW

  • KMID: 1912476
  • Korean J Urol.
  • 1987 Jun;28(3):468-472.
Posterior urethral valve is the most common obstructive abnormality in male children affecting both Kidneys and likely arise from maldevelopment of the mesonephric duct. We report a case of posterior...
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Carcinosarcoma of the uterine cervix arising from Mullerian ducts

Kim M, Lee C, Choi H, Ko JK, Kang G, Chun KC

Carcinosarcomas of the uterine cervix are extremely rare. Cervical carcinosarcoma can be characterized by having two different origins: the Mullerian ducts and the mesonephric duct remnants. A 53-year-old Korean woman...
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A Case Report of Complete Testicular Feminization Syndrome with Rudimentary Salpinx

Jo JH, Park YB, Park TH, Jang WY, Kim DG, Kim KW, Kim DK, Yoon HW, Kim DH, Kim MW, Park ST

  • KMID: 2076267
  • Korean J Obstet Gynecol.
  • 2001 May;44(5):986-989.
The Complete testicular feminization syndrome is a hereditary syndrome characterized clinically by female phenotype with 46, XY karyotype and bilateral testes. There is a congenital insensitivity to androgens, transmitted...
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A Rare Case of Zinner's Syndrome with Ectopic Prostate and Triorchidism

Ko A, Lee ES, Park HJ, Lee JB, Choi BI

Zinner's syndrome is a rare congenital abnormality of the mesonephric duct. Unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral ejaculatory duct obstruction are the triad of maldevelopment of the...
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A Gartner duct cyst of the vagina causing dysuria and dyschezia in a Yorkshire Terrier

Kim HJ, Kim JK, Choi JH, Jang JY, Ban HJ, Seo JM, Lee MJ, Choi HY, Kim MK, Kim HW

A 5 year-old, intact female Yorkshire terrier was referred for dysuria and dyschezia. The radiographic and ultrasound examination showed a round shaped mass caudal to the urinary bladder that contained...
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A Case of Congenital Intramural Cyst of Uterus

Lee NH, Choi WS, Kim SW, Choi SH, Kim MJ, Kim TY, Baik KD, Son HI

  • KMID: 2077543
  • Korean J Obstet Gynecol.
  • 2005 Dec;48(12):3013-3016.
I experienced a case of a congenital intramural cyst of the uterine fundus. It was composed of a single layer of non-ciliated low cuboidal epithelium without associated with endometrial stroma...
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Descent of mesonephric duct to the final position of the vas deferens in human embryo and fetus

Jin ZW, Abe H, Hinata N, Li XW, Murakami G, Rodríguez-Vázquez JF

Because the ureter arises from the mesonephric or Wolffian duct (WD), the WD opening should migrate inferiorly along the urogenital sinus or future urethra. However, this process of descent has...
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Effect of antiandrogens upon the morphological development of gubernaculum and the testicular descent in rats

Han SW, Lee HY, Yang WI, Choi SK

  • KMID: 2036828
  • Korean J Urol.
  • 1992 Apr;33(2):239-249.
We evaluated the effect of antiandrogens on both fetal and adult rats, noting especially the morphological changes in the gubernaculum and testicular descent. Two antiandrogens, flutamide and 5a-reductase inhibitor 4-methyl-4-aza-5-pregnane-3-one-20[s] carboxylate...
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Clear cell carcinoma of bladder invading the posterior urethra

Lee JK, Lee MY, Lee KC, Kim SC, Nam SK

  • KMID: 2114923
  • Korean J Urol.
  • 1992 Oct;33(5):900-903.
Clear cell carcinoma of the bladder and urethra is very rare entity with its origin unclear. The typical location in the bladder neck and trogon tends to confirm that this...
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Primary Malignant Tumor of the Retrovesical Region in Infancy

Yang KY

  • KMID: 1679485
  • Korean J Urol.
  • 1967 Jun;8(1):63-67.
Primary malignant tumors in the retrovesical region are extremely rare and are scarcely any in childhood. In the vast majority of the reported cases designated as primary malignant tumors of...
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Congenital Urethrovaginal Fistula Combined with Uterine Didelphia, Vaginovaginal Fistula and Single Kidney

Choi EY, Lee DS, Kim DS, Kim T, Cho JH

  • KMID: 2290468
  • Korean J Urol.
  • 1998 Nov;39(11):1154-1157.
Congenital urethrovaginal fistula is a rare disease. And also, combining with other congenital anomalies such as mesonephric duct defect is extremely rare. Mesonephric duct defect occurs in the 4th week...
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A Case of Clear Cell Adenocarcinoma in the Uterine Cervix of 22 Years-Old Virgin

Kim CJ, Park CS, Lee JW, Lee SH, Lee SJ, Kim BG, Lee JH, Bae DS

  • KMID: 2077070
  • Korean J Obstet Gynecol.
  • 2004 Jul;47(7):1409-1414.
Clear cell carcinoma of the uterine cervix is rare malignancy that accounts for 4% to 9% of the adenocarcinoma of the cervix. It is thought to originate from Mullerian duct,...
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