- A Case of 46XX, Primary Amenorrhea, Absent Gonads and Lack of Mullerian Ducts
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Lee BJ
- KMID: 1891267
- Korean J Fertil Steril.
- 2001 Jun;28(2):169-171.
OBJECTIVE: To study the etiology of primary amenorrhea in 19-aged woman. MATERIALS ANDMETHODS: Case report. RESULTS: I found that there were not gonads and organ of mullerian ducts origin on diagnostic laparoscopy.... -
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- A case of persistent Mullerian duct syndrome
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Han M, Kim SW, Seo KS, Cho HG, Rim JS
- KMID: 2289714
- Korean J Urol.
- 1991 Aug;32(4):682-684.
A small number of patients have been described in whom normal male development of the external genitalia has occurred but whom the Mullerian ducts persist. The retention of Mullerian structures... -
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- The Case of Prostaic Cystadenoma Which is Misdiagnosed as Mullerian Duct Cyst
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Kang JP, Lee SH, Lee YC, Shim BS, Kwon SW
- KMID: 1964453
- Ewha Med J.
- 2001 Jun;24(2):91-94.
- doi: 10.12771/emj.2001.24.2.91
Based on urological statistic results, finding a cyst in prostate are not common cases. The size of cysts are usually smaller than prostate and they are also generally found within... -
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- Carcinosarcoma of the uterine cervix arising from Mullerian ducts
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Kim M, Lee C, Choi H, Ko JK, Kang G, Chun KC
- KMID: 2148939
- Obstet Gynecol Sci.
- 2015 May;58(3):251-255.
- doi: 10.5468/ogs.2015.58.3.251
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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- Currarino triad with Mullerian duct anomaly in mother and daughter without MNX1 gene mutation
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Kim SH, Paek SH, Kim HY, Jung SE, Park KW
- KMID: 2149932
- Ann Surg Treat Res.
- 2016 Jan;90(1):49-52.
- doi: 10.4174/astr.2016.90.1.49
The Currarino triad is a unique complex of congenital caudal anomalies, including anorectal malformation, sacral bony defect and presacral mass. This triad may be associated with Mullerian duct anomalies, such... -
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- A case of unicornuate uterus with noncommunicating rudimentary horn with ipsilateral renal agenesis
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Chung JE, Kwon DJ, Kil KC
- KMID: 1475019
- Korean J Obstet Gynecol.
- 2009 Mar;52(3):382-386.
Rudimentary uterus with ipsilateral renal agenesis is a very rare mullerian duct malformation. The unicornuate uterus is a rare type of the anomalous uteri, which is caused by failure of... -
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- The current status of three-dimensional ultrasonography in gynaecology
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Ong CL
- KMID: 2382015
- Ultrasonography.
- 2016 Jan;35(1):13-24.
- doi: 10.14366/usg.15043
Ultrasonography (US) is the most recent cross-sectional imaging modality to acquire three-dimensional (3D) capabilities. The reconstruction of volumetric US data for multiplanar display took a significantly longer time to develop... -
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- Mullerian inhibiting substance/anti-Mullerian hormone: A novel treatment for gynecologic tumors
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Kim JH, MacLaughlin DT, Donahoe PK
- KMID: 2051715
- Obstet Gynecol Sci.
- 2014 Sep;57(5):343-357.
- doi: 10.5468/ogs.2014.57.5.343
Mullerian inhibiting substance (MIS), also called anti-Mullerian hormone (AMH), is a member of the transforming growth factor-beta super-family of growth and differentiation response modifiers. It is produced in immature Sertoli... -
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- Ectopic ovarian mixed epithelial tumor simulating colon cancer in a woman with a unicornuate uterus
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Lee JY, Yoon SW, Yoon SE, Ha KH, Park JK, Park JY, Jeong HS
- KMID: 2258141
- Korean J Med.
- 2009 Aug;77(Suppl 1):S192-S196.
Ovarian malignancy can rarely present as a colonic mass and simulate colon cancer. Mullerian anomalies are congenital anatomic abnormalities of the female internal genitalia, of which a unicornuate uterus is... -
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- A Case of Transverse Vaginal Septum with Microperforation Which got Pregnant by Intrauterine Insemination
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Nam YS, Kim NK, Kim JW, Lee CN, Cha KY
- KMID: 2262357
- Korean J Obstet Gynecol.
- 2001 Aug;44(8):1544-1548.
The mullerian ducts join the sinovaginal bulb at a point known as the mullerian tubercle. Canalization of the mullerian tubercle and sinovaginal bulb is necessary to give a normal vaginal... -
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- A Case of Vaginal Construction with Ileum
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Ryu CO, Lee HM, Kim WJ
- KMID: 2139416
- Korean J Urol.
- 1994 May;35(5):562-565.
Congenital vaginal atresia is rare and occurs as a result of aplasia of the mullerian ducts This is a source of great embarrassment and distress to patients and their close... -
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- Paraovarian Serous Borderline Tumor: A Case Report
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Hwang ET, Kim SH, Kim MJ, Kang YN
- KMID: 2427382
- J Korean Soc Radiol.
- 2018 Dec;79(6):337-339.
- doi: 10.3348/jksr.2018.79.6.337
Parovarian cyst is usually simple cyst, and accounts for 10%–20% of adnexal masses. Borderline or malignant parovarian tumor is rare, and it contains papillary projection at the smooth inner wall.... -
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- A Case of Rudimentary Uterine Horn Adenomyosis Associated With Agenesis of a Kidney, Pelvic Endometriosis
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Gu HJ, Rhee SJ, Suh MJ, Choi WJ, Lee SA, Lee JH, Paik WY
- KMID: 2075959
- Korean J Obstet Gynecol.
- 1999 Nov;42(11):2609-2613.
The unicornuate uterus is a rare type of the anomalous uteri, which is caused by failure of development of one of the mullerian ducts. This condition is usually associated with... -
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- A case of Herlyn-Werner-Wunderlich syndrome: a rare, congenital genitourinary anomaly in a 12-year-old girl
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Park JW, Jung JY
- KMID: 2368373
- Pediatr Emerg Med J.
- 2016 Jun;3(1):32-35.
- doi: 10.0000/pemj.2016.3.1.32
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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- Uterine Didelphys with Blind Hemivagina, Hematocolpos, Ipsilateral Renal Agenesis (UD-BHRA) and BilateralOvarian Tumors: A Case Report
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Lee YR, Choi BI, Park HW, Kook SH
- KMID: 2201413
- J Korean Radiol Soc.
- 1998 Mar;38(3):519-522.
- doi: 10.3348/jkrs.1998.38.3.519
Uterine didelphys is a congenital malformation characterized by the presence of two separated hemiuteri andhemivaginas, due to lack of midfusion of the Mullerian ducts. We report a case of UD-BHRA(uterine... -
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- Clinical characteristics of women with Mullerian anomaly: Twenty years of experience at Asan Medical Center
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Jeon GH, Park YR, Shin YJ, Kim SH, Chae HD, Kim CH, Kang BM
- KMID: 2273943
- Korean J Obstet Gynecol.
- 2010 Jul;53(7):626-632.
- doi: 10.5468/kjog.2010.53.7.626
OBJECTIVE: To investigate the clinical characteristics and reproductive outcomes of women with Mullerian anomalies. METHODS: One hundred and eighty-six patients were diagnosed with Mullerian anomalies at the Asan Medical Center from... -
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- Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome in a Child with Idiopathic Precocious Puberty
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Kang B, Park SH, Kim DH, Lee BI, Kim MY, Lee JE
- KMID: 1803844
- Ann Pediatr Endocrinol Metab.
- 2012 Jun;17(2):126-129.
- doi: 10.6065/apem.2012.17.2.126
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare congenital disorder characterized by the congenital absence or hypoplasia of the uterus and the upper two thirds of the vagina due to mullerian duct... -
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- Six cases of laparoscopic assisted neovaginoplasty using pelvic peritoneal flap in MRKH syndrome
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Park SD, Lee JS, Lee GW, Lee KE, Koh YB, Yang JB, Lee KH
- KMID: 2273807
- Korean J Obstet Gynecol.
- 2009 Nov;52(11):1185-1190.
Vaginal agenesis is rare gynecologic condition, and the most common etiology is Mayer-Rokitansky-Kster-Hauser (MRKH) syndrome, characterized by the absence of uterus and vagina and presence of normal ovaries and tubes.... -
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- Two Cases of Herlyn-Werner-Wunderlich Syndrome Diagnosed in Perinatal Period
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Ahn JH, Shin SH, Lee J, Sohn JA, Lee JA, Choi CW, Kim EK, Kim HS, Kim BI, Choi JH
- KMID: 2052469
- Neonatal Med.
- 2013 Feb;20(1):159-166.
- doi: 10.5385/nm.2013.20.1.159
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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- A case of ovarian cancer developed in Mayer-Rokitansky-Kuster-Hauser syndrome: Innate carcinogenesis of ovarian cancer
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Ko AR, Kim JH, Park SY, Jeon YE, Kim SJ, Rhim CC, Kang JB, Park YH
- KMID: 2274214
- Korean J Obstet Gynecol.
- 2012 Dec;55(12):1001-1005.
- doi: 10.5468/KJOG.2012.55.12.1001
Vaginal aplasia is an unusual congenital anomaly of the genital tract with an incidence of 1 in 4,000 female births. The vast majority of the cases are part of Mayer-Rokitansky-Kuster-Hauser... -
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