Division of Endocrinology, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
J Urol. 2017 Mar;197(3 Pt 2):937-943. doi: 10.1016/j.juro.2016.08.108. Epub 2016 Nov 10.
We sought to determine the presence of germ cells in the gonads of patients with disorders of sex development to establish whether preservation of germ cells for future fertility potential is possible. We hypothesized that germ cells are present but vary by age and diagnosis.
We reviewed histology from patients with disorders of sex development who underwent gonadectomy/biopsy from 2002 to 2014 at a single institution for pathological classification of the gonad, composition of gonadal stroma and germ cell presence.
A total of 44 patients were identified and germ cells were present in 68%. The presence and average number of germ cells per mm were analyzed by gonad type and diagnosis. By gonad type all ovotestes, most testes, ovaries and dysgenetic testes, and 15% of streak gonads had germ cells present. By diagnosis germ cells were present in all patients with complete androgen insensitivity syndrome, Denys-Drash syndrome, SRY mutation, mixed gonadal dysgenesis, ovotesticular conditions and StAR (steroid acute regulatory protein) deficiency, in some patients with persistent müllerian duct syndrome, XO/XY Turner syndrome and disorders of sex development not otherwise specified, and in none with complete or partial gonadal dysgenesis. Germ cells were present in the gonads of 88% of patients 0 to 3 years old, 50% of those 4 to 11 years old and 43% of those older than 12 years.
Germ cells were present in the majority of our cohort and the presence decreased with age. This novel, fertility driven evaluation of germ cell quantity in a variety of disorders of sex development suggests that fertility potential may be greater than previously thought. Further studies must be done to evaluate a larger population and examine germ cell quality to determine the viability of these germ cells.
我们旨在确定患有性发育障碍患者的性腺中是否存在生殖细胞,以确定是否有可能为未来的生育潜力保留生殖细胞。我们假设生殖细胞存在,但因年龄和诊断而异。
我们回顾了 2002 年至 2014 年期间在一家机构因性发育障碍而行性腺切除术/活检的患者的组织学资料,以对性腺进行病理分类、性腺基质的组成和生殖细胞的存在情况进行分类。
共确定了 44 例患者,其中 68%存在生殖细胞。根据性腺类型和诊断分析了生殖细胞的存在和平均每平方毫米的生殖细胞数量。按性腺类型,所有卵睾、大多数睾丸、卵巢和发育不良睾丸以及 15%的索状性腺中均存在生殖细胞。按诊断,所有完全雄激素不敏感综合征、Denys-Drash 综合征、SRY 突变、混合性腺发育不良、卵睾性疾病和 StAR(类固醇急性调节蛋白)缺乏症患者中均存在生殖细胞,一些持续性 Müllerian 管发育不全、XO/XY Turner 综合征和未明确的性发育障碍患者中存在生殖细胞,但完全或部分性腺发育不良患者中不存在生殖细胞。0 至 3 岁患者中 88%的性腺中存在生殖细胞,4 至 11 岁患者中 50%的性腺中存在生殖细胞,12 岁以上患者中 43%的性腺中存在生殖细胞。
在我们的大多数患者中存在生殖细胞,并且随着年龄的增长而减少。这项对各种性发育障碍患者生殖细胞数量的新型、以生育力为驱动的评估表明,生育潜力可能比以前认为的更大。需要进一步的研究来评估更大的人群,并检查生殖细胞的质量,以确定这些生殖细胞的活力。