Journals / Erciyes Tıp Dergisi / 2013 / Cilt: 35 - Sayı: 2

Term gebeliğe ulaşan Herlyn-Werner-Wunderlich sendromu: Nadir bir olgu sunumu

Herlyn-Werner-Wunderlich syndrome with term pregnancy: The presentation of a rare case

Pages
90–92
Publication Date
2022-10-17
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Right renal agenesis wasdiagnosed by abdominal CT taken after the cesarean section.Herlyn-Werner-Wunderlich syndrome is usually diagnosed after menarche, but in this case, it was diagnosed during a cae-sarean section.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Uterus didelphys with obstructed hemivagina and ipsilateralrenal agenesis is a rare entity referred to as Herlyn-Werner-Wunderlich syndrome.
📊
Key Findings & Data:In this article, we present a 21-year-old patient witha term pregnancy presenting with uterus didelphys, obstructedhemivagina, hematocolpos, and ipsilateral renal agenesis.
💡
Conclusion & Impact:Right renal agenesis wasdiagnosed by abdominal CT taken after the cesarean section.Herlyn-Werner-Wunderlich syndrome is usually diagnosed after menarche, but in this case, it was diagnosed during a cae-sarean section.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Uterus didelphys with obstructed hemivagina and ipsilateralrenal agenesis is a rare entity referred to as Herlyn-Werner-Wunderlich syndrome. It usually presents after menarche withremittent pelvic pain and a palpable pelvic mass due to hematocolpos. In this article, we present a 21-year-old patient witha term pregnancy presenting with uterus didelphys, obstructedhemivagina, hematocolpos, and ipsilateral renal agenesis. Anemergency cesarean section was performed because of fetaldistress. The fetus was in the left uterus, since due to hematocolpos, the right uterus was the size of 20 weeks of pregnancy.After delivery, the tip of ring forceps placed through the rightcervix was not seen in the vagina. Right renal agenesis wasdiagnosed by abdominal CT taken after the cesarean section.Herlyn-Werner-Wunderlich syndrome is usually diagnosed after menarche, but in this case, it was diagnosed during a cae-sarean section.

Özet

Herlyn-Werner-Wunderlich sendromu uterus didelfis, kör vajina ve ipsilateral renal agenezinin birlikte görüldüğü nadir bir durumdur. Genellikle menarş sonrası başlayan remittan pelvikağrı ve hematokolpos nedeniyle ele gelen kitle şikayetine sebep olur. Bu yazıda uterus didelfis, kör vajina ve aynı taraflı renal agenez saptanan term gebe 21 yaşında kadın hasta sunuldu. Hastanın gebeliği ultrasonografik ölçümlere göre 35haftalık idi. Fetal distres saptanması üzerine yapılan acil sezeryan girişiminde solda fetüsün bulunduğu uterus, sağda ise yaklaşık 20 hafta cesametinde diğer uterus gözlemlendi. Sağ uterustaki serviksten ilerletilen ring forsepsin ucunun vajinadan görülmedi belirlendi. Operasyondan sonra çekilen abdominaltomografide sağda renal agenez saptandı. Tanısı genellikle menarş sonrası konulan Herlyn-Werner-Wunderlich sendromuna,sunulan olguda olduğu gibi sezeryan sırasında da rastlanabilir.

🔖

Cite This Article

AL, R. A., YAPÇA, Ö. E., KARACA, İ., TALAR, Ş. (2022). Term gebeliğe ulaşan Herlyn-Werner-Wunderlich sendromu: Nadir bir olgu sunumu. Erciyes Tıp Dergisi, Cilt: 35 - Sayı: 2, 90–92. https://ajindex.com/articles/502403

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (6)

  1. Stassart JP Nagel TC, Prem KA, Phipps WR. Uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis: the University of Minnesota experience. Fertil Steril 1992; 57(4): 756-61
  2. Cox D, Ching BH
  3. Herlyn-Werner-Wunderlich syndrome: a rare presentation with pyocolpos. J Radiol Case Rep 2012; 6(3): 9-15
  4. Han BH, Park SB, Lee YJ, Lee KS, Lee YK. Uterus didelphys with blind hemivagina and ipsilateral renal agenesis (Herlyn-Werner-Wunderlich syndrome) suspected on the presence of hydrocolpos on prenatal sonography. J Clin Ultrasound 2012 Jun 7. doi: 10.1002/jcu.21950. [CrossRef] 4. Vivier PH, Liard A, Beurdeley M, Brasseur-Daudruy M, Cellier C, Le Dosseur P et al. Uterus didelphys, hemihydrocolpos and empty ipsilateral lumbar fossa in a newborn girl: involuted dysplastic kidney rather than renal agenesis. Pediatr Radiol 2011; 41(9): 1205-7. [CrossRef] 5. Kepkep N, Tezcan S, Ersoy Ü. Miadda gebelik ve komplet uterus bikornis. Turkiye Klinikleri J Gynecol Obst 2002; 12(2): 56-8
  5. Zurawin RK, Dietrich JE, Heard MJ, Edwards CL. Didelphic uterus and obstructed hemivagina with renal agenesis: case report and review of the literature. Pediatr Adolesc Gynecol 2004; 17(7): 137-41. [CrossRef] 7. Candiani GB, Fedele L, Candiani M. Double uterus, blind hemivagina, and ipsilateral renal agenesis: 36 cases and long-term follow-up. Obstet Gynecol 1997; 90(1): 26-32. [CrossRef] 8. Amesse LS, Ptaff-Amesse T. Congenital anomalies of the reproductive tract. In: Falcone T, Hurd WW, eds. Clinical Reproductive Medicine and Surgery 2007; 171(2): 235-9
  6. Kanakas N, Boos R, Schmidt W. Twin pregnancy in the right horn of a uterus didelphys: a case report. Eur J Obstet Gynecol Reprod Biol 1989; 32(3): 287-92. [CrossRef] 10. Heinonen PK. Clinical implications of the didelphic uterus: long-term follow-up of 49 cases. Eur J Obstet Gynecol Reprod Biol 2000; 91(2): 11183-90. [CrossRef] 11. Polat I. Herlyn-Wener-Wunderlich Sendromu: Uterus didelfis ile birlikte obstrükte hemivajen ve ipsilateral renal agenezi gösteren bir olgu serisi. Turkiye Klinikleri J Gynecol Obst 2008; 18(4): 284-8.