Infertility treatment in autosomal dominant polycystic kidney disease (ADPKD) - a case report


Orhan I., Onur R., Ergin E., Koksal I., Kadioglu A.

ANDROLOGIA, cilt.32, sa.2, ss.91-93, 2000 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 32 Sayı: 2
  • Basım Tarihi: 2000
  • Doi Numarası: 10.1046/j.1439-0272.2000.00335.x
  • Dergi Adı: ANDROLOGIA
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.91-93
  • İstanbul Üniversitesi Adresli: Hayır

Özet

Autosomal dominant polycystic kidney disease (ADPKD) is a frequently occurring inherited condition with cysts in many organs including the kidneys. However, a combination of seminal vesicle cysts, cystic obstruction of ejaculatory duct and ADPKD is rarely encountered. The following case report presents an infertile ADPKD patient who had seminal vesicle cysts and ejaculatory duct cyst, and describes the treatment by transurethral resection of the ejaculatory duct.