Zeng Wen-Heng, Xu Jiao-Jun, Jia Min-Yue, Ren Yue-Zhong
Department of Endocrinology and Metabolism, The Second Affiliated Hospital, Zhejiang University School of Medicine , Hangzhou, Zhejiang , China.
Gynecol Endocrinol. 2014 Oct;30(10):694-6. doi: 10.3109/09513590.2014.929654. Epub 2014 Jun 10.
To report the case of an individual with PHP, Turner syndrome and Hashimoto's thyroiditis.
A 16-year-old girl was referred to our hospital with chief complaint of short stature. She presented with round chubby facies, short neck, obesity and short stature. Radiography indicated short metatarsals and metacarpals, which mainly affected the second, third and fourth digits. Biochemistry revealed hyperphosphatemia, increased serum concentrations of parathyroid hormone and thyroid stimulating hormone, elevated levels of follicular-stimulating hormone and prolactin, and increased thyroid peroxidase antibody and thyroglobulin antibody. Radiographic examination revealed delayed bone age and pelvic ultrasonography demonstrated an immature uterus. Karyotype analysis showed 46,X,i(Xq10), while molecular analysis revealed a same sense mutation in exon 5 of GNAS (ATC → ATT, Ile).The specific diagnosis was made of Turner syndrome in the presence of Hashimoto's thyroiditis and PHP. She was treated with calcium supplementation, calcitriol and thyroxine.
This is the first case report to describe a combination of Turner syndrome with these other clinical entities, and their co-existence should be considered and further investigated.
报告一例患有假性甲状旁腺功能减退症(PHP)、特纳综合征和桥本甲状腺炎的患者。
一名16岁女孩因身材矮小为主诉被转诊至我院。她表现为圆脸、颈部短、肥胖及身材矮小。X线检查显示跖骨和掌骨短,主要累及第二、三、四指。生化检查显示高磷血症、甲状旁腺激素和促甲状腺激素血清浓度升高、促卵泡激素和催乳素水平升高,以及甲状腺过氧化物酶抗体和甲状腺球蛋白抗体增加。X线检查显示骨龄延迟,盆腔超声检查显示子宫未成熟。核型分析显示为46,X,i(Xq10),而分子分析显示GNAS外显子5存在同义突变(ATC→ATT,异亮氨酸)。确诊为特纳综合征合并桥本甲状腺炎和PHP。给予补充钙剂、骨化三醇和甲状腺素治疗。
这是首例描述特纳综合征与其他这些临床病症合并存在的病例报告,应考虑并进一步研究它们的共存情况。