11β-羟化酶缺陷症合并亚急性甲状腺炎致严重低血钾1例报道及文献复习  

11β-Hydroxylase deficiency combined with subacute thyroiditis resulting in severe hypokalemia: A case report and literature review

作　　者：付丽红 李丽华 刘璐[1] 李晓华[1] 张宏利 Fu Lihong;Li Lihua;Liu Lu;Li Xiaohua;Zhang Hongli(Department of Endocrinology Shanghai Seventh People′s Hospital Affiliated to Shanghai University of Traditional Chinese Medicine,Shanghai 200137,China)

机构地区：[1]上海中医药大学附属第七人民医院内分泌科,上海200137

出　　处：《中华内分泌代谢杂志》2024年第5期436-439,共4页Chinese Journal of Endocrinology and Metabolism

摘　　要：11β-羟化酶缺陷症(11β-hydroxylase deficiency, 11β-OHD)是常染色体隐性遗传性疾病先天性肾上腺皮质增生症中相对少见的一个类型, 本文报道了我院收治的1例11β-OHD合并亚急性甲状腺炎致严重低血钾的诊治情况并复习相关文献。11β-Hydroxylase deficiency(11β-OHD)is a relatively rare type of autosomal recessive hereditary disease congenital adrenal cortical hyperplasia.This article reports the diagnosis and treatment of a case of 11β-OHD combined with subacute thyroiditis leading to severe hypokalemia treated in our hospital,along with a review of relevant literature.

关 键 词：11β-羟化酶缺陷症 甲状腺毒症 亚急性甲状腺炎 低钾血症 

分 类 号：R581.4[医药卫生—内分泌] R586[医药卫生—内科学]