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.

引用

页数：6

共 28 条

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