Herlyn-Werner-Wunderlich Syndrome: A Mini-review
2
조회
0
다운로드
1
인용
0
참고문헌
키워드
초록
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital malformation syndrome that is characterized by a triad of uterine didelphys, blind hemivagina, and ipsilateral renal agenesis. There is a wide variety of phenotypic presentation which is recognized as a spectrum of disease rather than a separate entity. The exact incidence and pathogenesis of HWW syndrome are yet to be investigated. While this disease typically involves adolescent girls who present with abdominal pain or a pelvic mass that is secondary to hematocolpos, nowadays, a majority of potential patients with HWW are being prenatally screened for renal anomalies. Therefore, it is recommended to search for uterovaginal anomalies whenever a multicystic dysplastic kidney or the absence of a kidney is noted in a newborn female, and the role of pediatric nephrologists has become ever more important for early recognition of the disease.
Abstract
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital malformation syndrome that is characterized by a triad of uterine didelphys, blind hemivagina, and ipsilateral renal agenesis. There is a wide variety of phenotypic presentation which is recognized as a spectrum of disease rather than a separate entity. The exact incidence and pathogenesis of HWW syndrome are yet to be investigated. While this disease typically involves adolescent girls who present with abdominal pain or a pelvic mass that is secondary to hematocolpos, nowadays, a majority of potential patients with HWW are being prenatally screened for renal anomalies. Therefore, it is recommended to search for uterovaginal anomalies whenever a multicystic dysplastic kidney or the absence of a kidney is noted in a newborn female, and the role of pediatric nephrologists has become ever more important for early recognition of the disease.
참고문헌 (32)
- Orazi C, "Herlyn-Werner-Wunderlich syndrome: uterus didelphys, blind hemivagina and ipsilateral renal agenesis. Sonographic and MR findings in 11 cases", Pediatr Radiol, 37, pp.657~665 (2007)[DOI]
- Candiani GB, "Double uterus, blind hemivagina, and ipsilateral renal agenesis: 36 cases and long-term follow-up", Obstet Gynecol, 90, pp.26~32 (1997)[DOI]
- Smith NA, "Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome: management and followup", Fertil Steril, 87, pp.918~922 (2007)[DOI]
- George Wilson J, "A case of double uterus and vagina with unilateral hematocolpos and hematometra", J Obstet Gynaecol Br Emp, 32, pp.127~128 (1925)[DOI]
- Herlyn U, "Simultaneous occurrence of an open Gartnerduct cyst, a homolateral aplasia of the kidney and a double uterus as a typical syndrome of abnormalities", Geburtshilfe Frauenheilkd, 31, pp.340~347 (1971)
- Wunderlich M, "Unusual form of genital malformation with aplasia of the right kidney", Zentralbl Gynakol, 98, pp.559~562 (1976)
- Santos XM, "Obstructed Hemivagina with Ipsilateral Renal Anomaly", J Pediatr Adol Gynec, 29, pp.7~10 (2016)[DOI]
- Vercellini P, "Asymmetric lateral distribution of obstructed hemivagina and renal agenesis in women with uterus didelphys: institutional case series and a systematic literature review", Fertil Steril, 87, pp.719~724 (2007)[DOI]
- Fedele L, "Double uterus with obstructed hemivagina and ipsilateral renal agenesis: pelvic anatomic variants in 87 cases", Hum Reprod, 28, pp.1580~1583 (2013)[DOI]
- "The American Fertility Society classifications of adnexal adhesions, distal tubal occlusion, tubal occlusion secondary to tubal ligation, tubal pregnancies, mullerian anomalies and intrauterine adhesions", Fertil Steril, 49, pp.944~955 (1988)[DOI]
- Wang S, "Duplicated uterus and hemivaginal or hemicervical atresia with ipsilateral renal agenesis: an institutional clinical series of 52 cases", Eur J Obstet Gynaecol Reprod Biol, 170, pp.507~511 (2013)[DOI]
- Hall-Craggs MA, "Renal and urological abnormalities occurring with Mullerian anomalies", J Pediatr Urol, 9, pp.27~32 (2013)[DOI]
- Angthong W, "Herlyn-Werner-Wunderlich syndrome emphasizes ultrasonographic and MR findings: a case report and review of the literatures", J Med Assoc Thai, 95(Suppl 12), pp.S129~S133 (2012)
- Wu TH, "Herlyn-Werner-Wunderlich syndrome consisting of uterine didelphys, obstructed hemivagina and ipsilateral renal agenesis in a newborn", Pediatr Neonatol, 53, pp.68~71 (2012)[DOI]
- Gholoum S, "Management and outcome of patients with combined vaginal septum, bifid uterus, and ipsilateral renal agenesis (Herlyn-Werner-Wunderlich syndrome)", J Pediatr Surg, 41, pp.987~992 (2006)[DOI]
- Tong J, "Clinical characteristics of 70 patients with Herlyn-Werner-Wunderlich syndrome", Int J Gynaecol Obstet, 121, pp.173~175 (2013)[DOI]
- Coskun A, "Uterus didelphys with an obstructed unilateral vagina by a transverse vaginal septum associated with ipsilateral renal agenesis, duplication of inferior vena cava, high-riding aortic bifurcation, and intestinal malrotation: a case report", Fertil Steril, 90, pp.2006 e9~2006 e11 (2008)
- Pieroni C, "Uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis. A case report", J Reprod Med, 46, pp.133~136 (2001)
- Sardanelli F, "Uterus didelphys with blind hemivagina and ipsilateral renal agenesis: MR findings before and after vaginal septum resection", Eur J Radiol, 19, pp.164~170 (1995)[DOI]
- Tanaka YO, "Uterus didelphys associated with obstructed hemivagina and ipsilateral renal agenesis: MR findings in seven cases", Abdom Imaging, 23, pp.437~441 (1998)[DOI]
- Hoeffel C, "Uterus didelphys, obstructed hemivagina and ipsilateral renal agenesis", Eur J Radiol, 25, pp.246~248 (1997)[DOI]
- Zurawin RK, "Didelphic uterus and obstructed hemivagina with renal agenesis: case report and review of the literature", J Pediatr Adol Gynecol, 17, pp.137~141 (2004)[DOI]
- Guducu N, "Herlyn-Werner-Wunderlich syndrome--timely diagnosis is important to preserve fertility", J Pediatr Adol Gynecol, 25, pp.e111~e112 (2012)[DOI]
- Fedele L, "Endometriosis and nonobstructive mullerian anomalies", Obstet Gynecol, 79, pp.515~517 (1992)
- Ugur M, "Endometriosis in association with mullerian anomalies", Gynecol Obstet Inves, 40, pp.261~264 (1995)[DOI]
- Acien P, "Complex genital malformation: ectopic ureter ending in a supposed mesonephric duct in a woman with renal agenesis and ipsilateral blind hemivagina", Eur J Obstet Gynaecol Reprod Biol, 117(1), pp.105~108 (2004)[DOI]
- Capito C, "Pitfalls in the diagnosis and management of obstructive uterovaginal duplication: a series of 32 cases", Pediatrics, 122, pp.e891~e897 (2008)[DOI]
- Wang ZJ, "Ectopic ureter associated with uterine didelphys and obstructed hemivagina: preoperative diagnosis by MRI", Pediatr Radiol, 40, pp.358~360 (2010)[DOI]
- Westland R, "Risk factors for renal injury in children with a solitary functioning kidney", Pediatrics, 131, pp.e478~e485 (2013)[DOI]
- Acien P, "Reproductive performance of women with uterine malformations", Hum Reprod, 8, pp.122~126 (1993)[DOI]
- Haddad B, "Blind hemivagina: long-term follow-up and reproductive performance in 42 cases", Hum Reprod, 14, pp.1962~1964 (1999)[DOI]
- Olive DL, "Endometriosis and mullerian anomalies", Obstetr Gynecol, 69, pp.412~415 (1987)
