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| A case of autoimmune polyendocrine syndromes and literature review |
| ZHANG Liting1 WU Hao1 ZHU Lingling1 CAI Quanfang1 CHEN Pin2▲ |
1.Department of Endocrinology, the 910th Hospital of the Chinese People′s Liberation Army, Fujian Province, Quanzhou 362000, China;
2.Department of Endocrinology, the 90th Hospital of the Chinese People′s Liberation Army, Fujian Province, Fuzhou 350025, China |
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Abstract One case of autoimmune polyendocrine syndromes (APS) was reported and the literatures were reviewed in this paper for improve the diagnosis and treatment of the disease by clinicians. The patient was diagnosed with “type 1 diabetes” in June 2017 in the 910th Hospital of the Chinese People′s Liberation Army, the adult female represented with symptomatic “Hashimoto′s thyroiditis” in March 2018. She showed “primary hypogonadism” through examination in June 2019, and diagnosed with “APS-Ⅱ”. According to the etiology and clinical characteristics, APS was divided into two types: APS-Ⅰ and APS-Ⅱ. APS Ⅱ includes at least two of them among type 1 diabetes, Addison′s disease and autoimmune thyroid disease. Treatment is mainly involved in the exogenic hormone replacement for the function of corresponding endocrine glands and symptomatic treatment.
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