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以黄疸和血小板减少为表现的自身免疫性多腺体综合征。

Autoimmune polyglandular syndrome presenting with jaundice and thrombocytopenia.

作者信息

Norasyikin A W, Rozita M, Mohd Johan M J, Suehazlyn Z

机构信息

Pusat Perubatan Universiti Kebangsaan Malaysia (PPUKM), Kuala Lumpur, Malaysia.

出版信息

Med Princ Pract. 2014;23(4):387-9. doi: 10.1159/000357645. Epub 2014 Jan 7.

Abstract

OBJECTIVE

To report an uncommon presentation of a rare case of autoimmune polyglandular syndrome type IIIb in an elderly woman.

CLINICAL PRESENTATION AND INTERVENTION

A 62-year-old woman presented with anaemic symptoms and jaundice. Blood tests showed macrocytic anaemia due to vitamin B12 deficiency with Coombs negative haemolysis. A thyroid function test was consistent with hypothyroidism. Autoimmune antibody assays were positive for anti-parietal cell, anti-intrinsic factor and anti-thyroid peroxidase antibodies. A final diagnosis of autoimmune thyroiditis with pernicious anaemia, which constituted autoimmune polyglandular syndrome type IIIb, was made and the patient was treated with L-thyroxine, vitamin B12 injection and a blood transfusion. She was discharged uneventfully after a week of hospitalization.

CONCLUSION

This case showed that the presence of one autoimmune endocrine disease should prompt clinicians to look for other coexisting autoimmune diseases which may be asymptomatic despite positive autoantibodies.

摘要

目的

报告一名老年女性罕见的IIIb型自身免疫性多腺体综合征的不寻常表现。

临床表现与干预

一名62岁女性出现贫血症状和黄疸。血液检查显示因维生素B12缺乏导致的大细胞性贫血,且库姆斯试验阴性溶血。甲状腺功能检查结果符合甲状腺功能减退。自身免疫抗体检测显示抗壁细胞、抗内因子和抗甲状腺过氧化物酶抗体呈阳性。最终诊断为自身免疫性甲状腺炎伴恶性贫血,构成IIIb型自身免疫性多腺体综合征,患者接受左甲状腺素、维生素B12注射和输血治疗。住院一周后顺利出院。

结论

该病例表明,存在一种自身免疫性内分泌疾病应促使临床医生寻找其他并存的自身免疫性疾病,尽管自身抗体呈阳性,但这些疾病可能无症状。

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