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Cardiomyopathy and Pseudopuberty in a Girl With Severe Hypothyroidism due to Autoimmune Thyroiditis

机译:自身免疫性甲状腺炎导致严重甲状腺功能低下的女孩的心肌病和假青春期

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We report a 12-year-old girl with long-standing severe hypothyroidism due to autoimmune thyroiditis. She presented with congestive heart failure as a result of dilated cardiomyopathy, multiple-valve regurgitation, and pericardial effusion. She also had severe short stature (-5 standard deviation) and profound retarded bone age (3 years). Despite severe growth retardation, she had breast development without galactorrhea. She had a prepubertal response to luteinizing hormone-releasing hormone. Multicystic ovaries were noted on pelvic sonography. Magnetic resonance imaging of the brain revealed pituitary hyperplasia. Treatment with L-thyroxine and digoxin was promptly initiated with a subsequent clinical improvement and near-normal thyroid function tests. Unfortunately, she developed digitalis intoxication at 6 weeks, and eventually expired. Thus, titrating the dose of digoxin and frequent monitoring of serum digoxin levels are essential to prevent digitalis intoxication in the hypothyroid patient.
机译:我们报告了一名12岁女孩,由于自身免疫性甲状腺炎而长期患有严重的甲状腺功能减退症。由于扩张型心肌病,多瓣关闭不全和心包积液,她出现充血性心力衰竭。她的身材矮小严重(标准偏差为-5),骨龄严重延迟(3岁)。尽管严重发育迟缓,但她的乳房发育无溢乳。她对黄体激素释放激素有青春期前的反应。盆腔超声检查发现多囊卵巢。脑部的磁共振成像显示垂体增生。立即开始使用L-甲状腺素和地高辛治疗,随后的临床改善和甲状腺功能测试接近正常。不幸的是,她在6周时出现了洋地黄中毒,并最终死亡。因此,滴定地高辛的剂量和经常监测血清地高辛水平对于预防甲状腺功能减退患者的洋地黄中毒至关重要。

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