Metrika članka

  • citati u SCindeksu: 0
  • citati u CrossRef-u:0
  • citati u Google Scholaru:[=>]
  • posete u poslednjih 30 dana:4
  • preuzimanja u poslednjih 30 dana:1
članak: 1 od 21  
Back povratak na rezultate
Vojnosanitetski pregled
2019, vol. 76, br. 7, str. 749-752
jezik rada: engleski
vrsta rada: prikaz slučaja
doi:10.2298/VSP170113148R

Creative Commons License 4.0
Dvostruka materica udružena sa endometriozom jajnika kod infertilne pacijentkinje
aUniverzitet u Beogradu, Medicinski fakultet, GAK 'Narodni front'
bClinic of Gynecology and Obstetrics "Narodni Front", Belgrade + University of Belgrade, Faculty of Medicine, Belgrade

e-adresa: rudic.biljic@gmail.com

Sažetak

Uvod. Dvostruka materica nastaje kada potpuno izostane fuzija Milerovih kanala. U radu je prikazan redak entitet dvostruke materice neopstruktivnog tipa, udružene sa endometriotičnom cistom jajnika. Prikaz bolesnika. Pacijentkinja stara 29 godina, nulipara, primljena je na našu kliniku za laparoskopsku operaciju endometriotične ciste jajnika. Bimanuelnim ginekološkim pregledom i transvaginalnim 2D ultrazvukom dijagnostikovana je endometriotična cista desnog jajnika i dvostruka materica neopstruktivnog tipa. Dijagnoza je kasnije potvrđena laparoskopijom i magnetnom rezonancom. Urađena je laparoskopska incizija i drenaža sadržaja ciste, sa biopsijom i koagulacijom endometriotičnog žarišta. Patohistološki je potvrđena endometrioza jajnika. Postoperativno pacijentkinji je ordiniran analog gonadotropin oslobađajućeg hormona, u vremenu od tri meseca. Deset meseci nakon završenog kompletnog tretmana, pacijentkinja je bila bez recidiva bolesti. Zaključak. Dvostruka materica neopstruktivnog tipa je retko udružena sa endometriozom jajnika.

Ključne reči

Reference

Novododat članak: provera, normiranje i linkovanje referenci u toku.
Grimbizis GF, Camus M, Tarlatzis BC, Bontis JN, Devroey P. Clinical implications of uterine malformations and hysteroscopic treatment results. Hum Reprod Update 2001; 7(2): 161-74
Gomathy E, Sheela SR, Lakshmi G. Uterus didelphys with unilateral vaginal obstruction having single pregnancy in her right horn: A case report. J Clin Biomed Sci 2013; 3(3): 143-5
Rudra S, Dahiya N. OHVIRA syndrome: A rare variant of mullerian duct anomaly. Int J Reprod Contracept Obstet Gynecol 2017; 6(1): 326-8
Tong J, Zhu L, Chen N, Lang J. Endometriosis in association with Herlyn-Werner-Wunderlich syndrome. Fertil Steril 2014; 102(3): 790-4
Karaca L, Pirimoglu B, Bayraktutan U, Ogul H, Oral A, Kantarci M. Herlyn-Werner-Wunderlich syndrome: A very rare urogenital anomaly in a teenage girl. J Emerg Med 2015; 48(3): e73-5
Alborzi S, Tavana Z, Amini M. Hysteroscopic resection of vaginal septum in didelphys uteruswith hemiobstructed vagina. J Minim Invasive Surg Sci 2014; 3(2): e13573
Sabdia S, Sutton B, Kimble RM. The obstructed hemivagina, ipsilateral renal anomaly, and uterine didelphys triad and the subsequent manifestation of cervical aplasia. J Pediatr Adolesc Gynecol 2014; 27(6): 375-8
Chan YY, Jayaprakasan K, Zamora J, Thorton JG, Raine-Fenning N, Comarasamy A. The prevalence of congenital uterine anomalies in unselected and high-risk populations: a systematic review. Hum Reprod 2011; 17(6): 761-71
Di Spiezio Sardo A, Campo R, Gordts S, Spinelli M, Cosimato C, Tanos V, et al. The comprehensiveness of the ESHRE/ESGE classification of female genital tract congenital anomalies: A systematic review of cases not classified by the AFS system. Hum Reprod 2015; 30(5): 1046-58
Bholl R, Ahluwalla A, Chauhan N. Herlyn Werner Wunderlich Syndrome with hematocolpos: An unusual casereport of full diagnostic approach and treatment. Int J Fertil Steril 2016; 10(1): 136-40
Ali MK, Abdelbadee AY, Shazly SA, Abbas MA. Uterus didelphys with multiple fibroids: A case report. Proc Obstet Gynecol 2013; 3(2): Article 3 [4 p.]. Available from: http://ir.uiowa.edu/pog
Yang MJ, Tseng JY, Chen CY, Li HY. Delivery of double singleton pregnancies in a woman with a double uterus, double cervix, and complete septate vagina. J Chin Med Assoc 2016; 78(12): 746-8
Rezai S, Bisram P, Lora Alcantara I, Upadhyay R, Lara C, Elmadjian M. Didelphys Uterus: A Case Report and Review of the Literature. Case Rep Obstet Gynecol 2015; 2015: 865821
Fedele L, Motta F, Frontino G, Restelli E, Bianchi S. Double uterus with obstructed hemivagina and ipsilateral renal agenesis: Pelvic anatomic variants in 87 cases. Hum Reprod 2013; 28(6): 1580-3
Yavuz A, Bora A, Kurdoğlu M, Goya C, Kurdoğlu Z, Beyazal M, et al. Herlyn-Werner-Wunderlich syndrome merits of sonographic and magnetic resonance imaging for accurate diagnosis and patient management in 13 cases. Pediatr Adolesc Gynecol 2015; 28(1): 47-52