Congenital bilateral ejaculatory duct absence complicated with seminal vesicle cyst: a case report and review of the literature.
- Author:
Kai LIAO
;
Hua SHEN
;
Hong-fei WU
- Publication Type:Case Reports
- MeSH: Cysts; complications; diagnosis; Ejaculatory Ducts; abnormalities; Genital Diseases, Male; complications; diagnosis; Humans; Male; Retrospective Studies; Seminal Vesicles
- From: National Journal of Andrology 2015;21(2):161-164
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo report a case of simple congenital bilateral ejaculatory duct absence (EDA) complicated with seminal vesicle cyst and review the relevant literature in order to improve the diagnosis and treatment of the disease.
METHODSWe retrospectively reviewed the clinical data of a case of bilateral congenital EDA complicated with seminal vesicle cyst, reviewed the relevant literature at home and abroad, and comprehensively analyzed the embryonic development, diagnosis, and treatment of congenital EDA.
RESULTSThe patient was a 23-year-old man, present at the clinic for infertility after married for a year. Vasography and other imaging examinations confirmed simple congenital bilateral EDA complicated with seminal vesicle cyst. Pathologic biopsy showed normal spermatogenic function of the testes.
CONCLUSIONCongenital EDA originates from embryonic developmental defect of the mesonephric duct, and it can be confirmed by vasography. Transurethral incision of the ejaculatory duct and intracytoplasmic sperm injection can be employed for the treatment of bilateral EDA.