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假性低丙种球蛋白血症-伪装成普通变异性免疫缺陷的孟乔森综合征。

Hypogammaglobulinemia factitia- Munchausen syndrome masquerading as common variable immune deficiency.

出版信息

Allergy Asthma Clin Immunol. 2013 Sep 17;9(1):36. doi: 10.1186/1710-1492-9-36.

Abstract

BACKGROUND

We describe the first case of a patient with factitious disorder who closely simulated a primary immune deficiency disorder - Common Variable Immune Deficiency (CVID), by surreptitiously ingesting non-steroidal anti-inflammatory agents.

CASE DESCRIPTION

He was treated with several expensive and potentially dangerous drugs before the diagnosis was established through collateral information. In retrospect he did not meet the proposed new criteria for CVID. These criteria may prove useful in distinguishing cases of CVID from secondary hypogammaglobulinemia.

CONCLUSION

It is imperative clinicians recognise patients with factitious disorder at the earliest opportunity to prevent iatrogenic morbidity and mortality.

摘要

背景

我们描述了首例通过秘密服用非甾体类抗炎药物来模拟原发性免疫缺陷疾病 - 普通可变免疫缺陷(CVID)的诈病患者。

病例描述

在通过间接信息建立诊断之前,他已经接受了几种昂贵且可能危险的药物治疗。事后看来,他不符合新提出的 CVID 诊断标准。这些标准可能有助于将 CVID 与继发性低丙种球蛋白血症区分开来。

结论

临床医生必须尽早识别诈病患者,以防止医源性发病率和死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a99f/3848570/e75696f5f5ec/1710-1492-9-36-1.jpg

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