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An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis

We report the case of a 46-year-old Chinese male patient who visited our clinic complaining of infertility. Semen analysis revealed azoospermia, and azoospermia factor c region partial deletion (b1/b3) was detected using Y chromosome microdeletion analysis. Testicular sperm extraction was performed...

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Detalles Bibliográficos
Autores principales: Kuroda, Shinnosuke, Usui, Kimitsugu, Mori, Kohei, Yasuda, Kengo, Asai, Takuo, Sanjo, Hiroyuki, Yakanaka, Hiroyuki, Takeshima, Teppei, Kawahara, Takashi, Hamanoue, Haruka, Kato, Yoshitake, Miyoshi, Yasuhide, Uemura, Hiroji, Iwasaki, Akira, Yumura, Yasushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Reproductive Medicine 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897248/
https://www.ncbi.nlm.nih.gov/pubmed/29662826
http://dx.doi.org/10.5653/cerm.2018.45.1.48
Descripción
Sumario:We report the case of a 46-year-old Chinese male patient who visited our clinic complaining of infertility. Semen analysis revealed azoospermia, and azoospermia factor c region partial deletion (b1/b3) was detected using Y chromosome microdeletion analysis. Testicular sperm extraction was performed after genetic counseling. The bilateral ductus deferens and a portion of the epididymis were absent, whereas the remaining epididymis was expanded. Motile intratesticular spermatozoa were successfully extracted from the seminiferous tubule. On histopathology, nearly complete spermatogenesis was confirmed in almost every seminiferous tubule. To our knowledge, this is the first case report of b1/b3 deletion with a congenital bilateral absence of the vas deferens and almost normal spermatogenesis.