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一种典型的系统性血管炎模仿者。

A classic mimicker of systemic vasculitis.

作者信息

Moreno-Ariño Marc, Ortiz-Santamaria Vera, Deudero Infante Aída, Ayats Delgado Montserrat, Novell Teixidó Francesc

机构信息

Servicio de Geriatría, Hospital General de Granollers, Granollers, Barcelona, España.

Unidad de Reumatología, Servicio de Medicina Interna, Hospital General de Granollers, Granollers, Barcelona, España; Departamento de Medicina, Universidad Internacional de Catalunya, Sant Cugat del Vallès, Barcelona, España.

出版信息

Reumatol Clin. 2016 Mar-Apr;12(2):103-6. doi: 10.1016/j.reuma.2015.03.006. Epub 2015 Apr 30.

Abstract

BACKGROUND AND OBJECTIVE

Embolic and constitutional manifestations of intracavitary cardiac tumors are included within the classic mimickers of systemic vasculitis, especially in those in which there are no cardiac manifestations. We present a case report of atrial myxoma in which the patient only presented systemic symptoms and in whom an initial diagnostic approach of systemic vasculitis was made. We also performed a literature search of the cases described.

PATIENT AND METHOD

A case report of atrial myxoma with atypical presentation manifested as a systemic disease with no concomitant cardiac symptoms is described. The case report is discussed and 11 cases of atrial myxoma pseudovasculitis described in the literature are reviewed, emphasizing their similarities and differences.

DISCUSSION

Constitutional symptoms and cutaneous manifestations were the most common. Most of the cases showed partial response to glucococorticosteroid treatment, reinforcing the theory of the inflammatory role in its pathogenesis. Mean delayed time to diagnosis was 12.27 months.

CONCLUSION

Atrial myxoma is a systemic vasculitis mimicker, this being difficult to diagnose in the absence of cardiac manifestations. This delay in diagnosis entails serious complications.

摘要

背景与目的

心腔内肿瘤的栓塞和全身表现包括在系统性血管炎的典型模仿疾病范围内,特别是在那些没有心脏表现的疾病中。我们报告一例心房黏液瘤病例,该患者仅表现出全身症状,最初被诊断为系统性血管炎。我们还对已描述的病例进行了文献检索。

患者与方法

描述一例具有非典型表现的心房黏液瘤病例,该病例表现为一种无伴随心脏症状的全身性疾病。对该病例报告进行了讨论,并回顾了文献中描述的11例心房黏液瘤假血管炎病例,强调了它们的异同。

讨论

全身症状和皮肤表现最为常见。大多数病例对糖皮质激素治疗有部分反应,这强化了炎症在其发病机制中的作用理论。平均诊断延迟时间为12.27个月。

结论

心房黏液瘤是系统性血管炎的模仿疾病,在没有心脏表现的情况下难以诊断。这种诊断延迟会导致严重并发症。

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