Autoimmune polyglandular syndrome type 3: A case report of an unusual presentation and literature review

被引：4
作者：
Apolinario, Michael [1 ]
Brussels, Aaron [2 ]
Cook, Curtiss B. [3 ]
Yang, Shaun [4 ]
机构：
[1] Mayo Clin, Coll Med & Sci, Dept Internal Med, Scottsdale, AZ 85259 USA
[2] Mayo Clin, Dept Anesthesiol & Perioperat Med, Coll Med & Sci, Scottsdale, AZ USA
[3] Mayo Clin, Dept Internal Med, Div Endocrinol, Coll Med & Sci, Scottsdale, AZ USA
[4] Mayo Clin, Div Hosp Internal Med, Dept Internal Med, Coll Med & Sci, Scottsdale, AZ USA
来源：
CLINICAL CASE REPORTS | 2022年 / 10卷 / 02期
关键词：
autoimmune polyglandular syndrome; cobalamin deficiency; subacute combined degeneration; thyroid autoimmune disease; pernicious anemia; vitamin B12 deficiency; SUBACUTE COMBINED DEGENERATION; COBALAMIN VITAMIN-B-12; PARIETAL-CELL; PREVALENCE; GUIDELINES; ANTIBODIES; PATIENT; DISEASE;
D O I：
10.1002/ccr3.5391
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Autoimmune polyglandular syndromes (APS) are rare disorders characterized by auto-destruction of endocrine and non-endocrine organs by organ-specific antibody-directed T-lymphocytic infiltration. This case highlights a 29-year-old Caucasian man with vitiligo found to have significant neurological abnormalities in the setting of newly diagnosed pernicious anemia and thyroid autoimmune disease.
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页数：6
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