Autoimmune Polyglandular Syndrome II: A Case Report

被引:0
|
作者
Awad, Olfat [1 ]
Basma, Hadil [2 ]
Masri, Rim [2 ]
Hamadeh, Samih [3 ]
Hamadeh, Majdi [1 ,4 ]
机构
[1] Lebanese Univ, Fac Med Sci, Dept Nephrol, Beirut, Lebanon
[2] Lebanese Univ, Fac Med Sci, Dept ofEndocrinol, Beirut, Lebanon
[3] Wayne State Univ, Detroit Med Ctr, Dept Internal Med, Detroit, MI USA
[4] Al Zahraa Hosp Univ Med Ctr, Dept Nephrol, Beirut, Lebanon
关键词
siadh; hyponatremia; case report; aps ii; adrenal insufficiency; diabetes;
D O I
10.7759/cureus.52372
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Autoimmune polyglandular syndrome II (APS-II), also known as Schmidt syndrome, is a rare endocrine disorder characterized by endocrine and non -endocrine illnesses. Addison's disease and at least one additional autoimmune condition, such as autoimmune thyroid disease or type 1 diabetes mellitus (T1DM), are features of APS-II. It can result from genetic and non -genetic factors. We present a case of a 60 -year -old female patient with a history of T1DM and a recent diagnosis of Hashimoto's thyroiditis who was admitted to the nephrology department for hyponatremia. Investigations showed the presence of adrenal insufficiency (AI), so she was diagnosed with APS-II and had the full triad of this syndrome. Thus, it is important to think about the diagnosis of AI or other autoimmune conditions in a patient who already has one or more autoimmune diseases.
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页数:7
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