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一名成年起病的斯蒂尔病患者的类鼻疽血清学阳性:一例诊断困境的病例报告

Positive melioidosis serology in a patient with adult onset Still's disease: a case report of a diagnostic dilemma.

作者信息

Dissanayake Harsha Anuruddhika, Premawansa Gayani, Corea Enoka, Atukorale Inoshi

机构信息

1University Medical Unit, National Hospital of Sri Lanka, Colombo, Sri Lanka.

2Colombo North Teaching Hospital, Ragama, Sri Lanka.

出版信息

BMC Rheumatol. 2018 Dec 10;2:37. doi: 10.1186/s41927-018-0044-5. eCollection 2018.

Abstract

BACKGROUND

Autoimmune disorders are known to produce false positives in serological tests for infections. Aetiological association between infections and autoimmunity, increased susceptibility to infectious and autoimmune disorders with immune dysregulation and non-specific polyclonal expansion of B cells with autoimmunity may cause confusion in diagnosis and patient management. We report a patient with Adult Onset Still's Disease (AOSD) presenting with rising melioidosis antibody titres that caused diagnostic confusion.

CASE PRESENTATION

A forty-nine-year-old female presented with prolonged fever, sore-throat, large joint arthritis, lymphadenopathy, hepatomegaly and transient rash. She had elevated inflammatory markers and a rising melioidosis antibody titre. The patient responded poorly to prolonged course of appropriate antimicrobials but showed rapid and sustained improvement with glucocorticoids.

CONCLUSION

Positive melioidosis serology could have been due to a co-infection or false positive antibody reaction due to non-specific B cell expansion or an indicator of true infection that triggered the immune dysregulation to develop AOSD.

摘要

背景

自身免疫性疾病在感染的血清学检测中会产生假阳性。感染与自身免疫之间的病因学关联、免疫失调导致对感染性和自身免疫性疾病易感性增加以及自身免疫时B细胞的非特异性多克隆扩增,可能会在诊断和患者管理方面造成混淆。我们报告一例成年起病的斯蒂尔病(AOSD)患者,其类鼻疽抗体滴度升高导致诊断混乱。

病例介绍

一名49岁女性,出现持续发热、咽痛、大关节关节炎、淋巴结病、肝肿大和一过性皮疹。她的炎症指标升高,类鼻疽抗体滴度上升。该患者对适当的抗菌药物长疗程治疗反应不佳,但使用糖皮质激素后迅速且持续改善。

结论

类鼻疽血清学阳性可能是由于合并感染、非特异性B细胞扩增导致的假阳性抗体反应,或是触发免疫失调从而发展为AOSD的真正感染的一个指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a41f/6390555/e41fece25414/41927_2018_44_Fig1_HTML.jpg

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