Sloan M S, Rosenberg S M, Brown J A
Obstet Gynecol. 1984 Sep;64(3 Suppl):64S-67S. doi: 10.1097/00006250-198409001-00017.
A 24-year-old woman was evaluated for primary amenorrhea and virilization. Karyotyping revealed a rare dicentric Y chromosome with complex mosaicism. Subsequent total abdominal hysterectomy/bilateral salpingo-oophorectomy demonstrated true hermaphroditism manifested by a right ovotestis, a left streak gonad, and Mullerian structures on the right despite the presence of testicular tissue. With the exception of short stature, Turner stigmata were not present despite the predominance of a 45,X cell line. The literature is reviewed.
一名24岁女性因原发性闭经和男性化前来就诊。染色体核型分析显示存在一条罕见的双着丝粒Y染色体,伴有复杂的嵌合体现象。随后进行的全腹子宫切除术/双侧输卵管卵巢切除术显示为真两性畸形,表现为右侧卵睾、左侧条索状性腺,且尽管存在睾丸组织,但右侧仍有苗勒管结构。除身材矮小外,尽管45,X细胞系占优势,但并未出现特纳综合征体征。本文对相关文献进行了综述。