Skeletal Disorders & Mineral Homeostasis Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, 30 Convent Drive Room 218 MSC 4320, Bethesda, MD, USA.
Division of Pediatric and Adolescent Gynecology, Department of Obstetrics and Gynecology, MedStar Washington Hospital Center, Children's National Health System, Washington, D.C., USA.
Orphanet J Rare Dis. 2019 Apr 29;14(1):90. doi: 10.1186/s13023-019-1057-x.
Autonomous ovarian activation with recurrent estrogen-producing cysts is a hallmark feature of the rare bone and endocrine disorder fibrous dysplasia/McCune-Albright syndrome. Precocious puberty in girls with McCune-Albright syndrome has been well-described, however long-term effects on gynecologic and reproductive function are unknown. Concerningly, case reports have described poor skeletal outcomes associated with pregnancy in women with fibrous dysplasia.
Thirty-nine women with fibrous dysplasia/McCune-Albright syndrome were evaluated as part of a natural history study. Clinical, radiographic, and biochemical data were reviewed. Women were contacted to obtain detailed menstrual and reproductive histories.
Abnormal uterine bleeding affected 77% of women (30/39), and was associated with severe anemia requiring blood transfusion in 3 cases. Nine women underwent hysterectomy for management of bleeding, including 67% (6/9) at the unusually young age of less than age 35 years. Infertility affected 43% of women (9/21), including 2 women who developed primary ovarian insufficiency after undergoing surgical treatment of ovarian cysts. Of 25 spontaneous pregnancies in 14 women, 35% (8) were unplanned. Among the 14 pregnancies, pregnancy was associated with no change in bone pain in 7 subjects (53%), increased bone pain in 4 subjects (31%), and decreased bone pain in 2 subjects (15%). No additional skeletal complications were reported during pregnancies.
Women with fibrous dysplasia/McCune-Albright syndrome report a high prevalence of gynecologic morbidity and reduced fertility. There is no clear association between pregnancy and poor skeletal outcomes in this population.
具有复发性产生雌激素的囊肿的自主卵巢激活是罕见的骨骼和内分泌疾病纤维发育不良/ McCune-Albright 综合征的显著特征。 McCune-Albright 综合征女孩的性早熟已有很好的描述,但是对妇科和生殖功能的长期影响尚不清楚。令人担忧的是,病例报告描述了与患有纤维发育不良的妇女的妊娠相关的不良骨骼结局。
对 39 名纤维发育不良/ McCune-Albright 综合征妇女进行了评估,作为自然史研究的一部分。回顾了临床,放射学和生化数据。与妇女联系以获取详细的月经和生殖史。
异常子宫出血影响了 77%的妇女(30/39),其中 3 例因严重贫血需要输血。有 9 名妇女因出血而行子宫切除术,其中包括 67%(6/9)的年龄不到 35 岁。不孕影响了 43%的妇女(9/21),其中 2 名妇女在接受卵巢囊肿手术治疗后发生了原发性卵巢功能不全。在 14 名妇女的 25 次自发性妊娠中,有 35%(8 次)是意外妊娠。在 14 次妊娠中,有 7 名(53%)受试者的骨痛没有变化,4 名(31%)受试者的骨痛增加,2 名(15%)受试者的骨痛减少。怀孕期间没有报告其他骨骼并发症。
患有纤维发育不良/ McCune-Albright 综合征的妇女报告了较高的妇科发病率和生育力下降。在该人群中,妊娠与不良骨骼结局之间没有明确的关联。