医学
特纳综合征
甲状腺肿
格雷夫斯病
内科学
自身抗体
特纳综合征
甲状腺
内分泌系统
内分泌学
自身免疫
疾病
儿科
激素
抗体
免疫学
作者
정진욱,Dong Hyeok Cho,Dong-Jin Chung,ChungMinyoung
出处
期刊:The Korean Journal of Internal Medicine
日期:2008-01-01
卷期号:74 (3): 325-329
摘要
It is becoming increasingly evident that adults with Turner’s syndrome are susceptible to endocrine autoimmunity. An increased prevalence of thyroid autoantibodies and hypothyroidism in patients with Turner’s syndrome has been reported, but the involvement of Graves’ disease in these patients is relatively rare. We describe a case of Graves’ disease associated with Turner’s syndrome. A 28-year-old woman was referred for diffuse anterior neck swelling and palpitation. She had been diagnosed with Turner’s syndrome with monosomy 45,X before the age of 9 years and she took estrogen together with progesterone. The physical examination revealed a firm, non-tender goiter. The T3 level was 632 ng/dL, the free T4 level was 5.68 ng/dL, the TSH level was 0.02 µIU/mL, the % of TSH-binding inhibiting immunoglobulin was 24% and the anti-thyroid autoantibodies were positive. The radioactive iodine uptake was increased. Therefore, she was diagnosed as having Graves’ disease.
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