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锂作为格雷夫斯甲状腺毒症的替代选择。

Lithium as an Alternative Option in Graves Thyrotoxicosis.

作者信息

Prakash Ishita, Nylen Eric Sixtus, Sen Sabyasachi

机构信息

Department of Medicine, Division of Endocrinology & Metabolism, Medical Faculty Associates, The George Washington University, Washington, DC, USA.

出版信息

Case Rep Endocrinol. 2015;2015:869343. doi: 10.1155/2015/869343. Epub 2015 Sep 6.

Abstract

A 67-year-old woman was admitted with signs and symptoms of Graves thyrotoxicosis. Biochemistry results were as follows: TSH was undetectable; FT4 was >6.99 ng/dL (0.7-1.8); FT3 was 18 pg/mL (3-5); TSI was 658% (0-139). Thyroid uptake and scan showed diffusely increased tracer uptake in the thyroid gland. The patient was started on methimazole 40 mg BID, but her LFTs elevated precipitously with features of fulminant hepatitis. Methimazole was determined to be the cause and was stopped. After weighing pros and cons, lithium was initiated to treat her persistent thyrotoxicosis. Lithium 300 mg was given daily with a goal to maintain between 0.4 and 0.6. High dose Hydrocortisone and propranolol were also administered concomitantly. Free thyroid hormone levels decreased and the patient reached a biochemical and clinical euthyroid state in about 8 days. Though definitive RAI was planned, the patient has been maintained on lithium for more than a month to control her hyperthyroidism. Trial removal of lithium results in reemergence of thyrotoxicosis within 24 hours. Patient was maintained on low dose lithium treatment with lithium level just below therapeutic range which was sufficient to maintain euthyroid state for more than a month. There were no signs of lithium toxicity within this time period. Conclusion. Lithium has a unique physiologic profile and can be used to treat thyrotoxicosis when thionamides cannot be used while awaiting elective radioablation. Lithium levels need to be monitored; however, levels even at subtherapeutic range may be sufficient to treat thyrotoxicosis.

摘要

一名67岁女性因格雷夫斯甲状腺毒症的症状和体征入院。生化检查结果如下:促甲状腺激素(TSH)检测不到;游离甲状腺素(FT4)>6.99 ng/dL(0.7 - 1.8);游离三碘甲状腺原氨酸(FT3)为18 pg/mL(3 - 5);甲状腺刺激免疫球蛋白(TSI)为658%(0 - 139)。甲状腺摄取和扫描显示甲状腺内放射性示踪剂摄取弥漫性增加。患者开始服用甲巯咪唑,每日两次,每次40 mg,但她的肝功能检查急剧升高,出现暴发性肝炎的特征。确定甲巯咪唑为病因并停药。权衡利弊后,开始使用锂治疗她持续的甲状腺毒症。每天给予300 mg锂,目标是维持在0.4至0.6之间。同时还给予了高剂量氢化可的松和普萘洛尔。游离甲状腺激素水平下降,患者在约8天内达到生化和临床甲状腺功能正常状态。尽管计划进行确定性放射性碘(RAI)治疗,但患者已服用锂超过一个月以控制甲亢。停用锂的试验导致甲状腺毒症在24小时内复发。患者维持低剂量锂治疗,锂水平略低于治疗范围,这足以维持甲状腺功能正常状态超过一个月。在此期间没有锂中毒的迹象。结论。锂具有独特的生理特性,在不能使用硫代酰胺类药物而等待择期放射性消融时,可用于治疗甲状腺毒症。需要监测锂水平;然而,即使在亚治疗范围内的水平也可能足以治疗甲状腺毒症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daf2/4575726/2cfb88242d3f/CRIE2015-869343.001.jpg

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