| Literature DB >> 24839497 |
Abderrazak Bouzouita1, Walid Kerkeni1, Hassine Abouda2, Mohamed Khrouf2, Hanene Elloumi2, Najla Mnif3, Taieb Messaoud3, Amel Zhioua2, Fethi Zhioua2, Mohamed Chebil1.
Abstract
Seminal vesicle malformations are a rare cause of obstructive azoospermia, often associated with other internal genitalia and upper urinary tract birth defects. We report 5 new cases of seminal vesicle agenesis in men presenting with hypospermia and azoospermia. Imaging showed seminal vesicle unilateral agenesis in all patients. The remaining seminal vesicle was hypoplastic in 3 cases, dilated in 1 case and with abnormally thick content in another case. Vas deferens agenesis was observed unilaterally in 2 patients and bilaterally in 2 other patients. No renal malformations were detected. Genetic study showed in all cases a 46 XY karyotype without any microdeletions. A single heterozygous cystic fibrosis transmembrane regulator gene mutation was diagnosed in 1 man, but not found in his partner. Intracytoplasmic sperm injection using sperm from a testicular biopsy was performed in 3 couples, without success.Entities:
Year: 2014 PMID: 24839497 PMCID: PMC4001658 DOI: 10.5489/cuaj.1663
Source DB: PubMed Journal: Can Urol Assoc J ISSN: 1911-6470 Impact factor: 1.862