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[原发性干燥综合征:外分泌和非外分泌表现]

[Primary Sjögren's syndrome: exocrine and non-exocrine manifestations].

作者信息

Muñoz Maria da Graça Henriques da Conceição Negrão Sequeira, Castelão Walter Carlos Baptista, Saraiva Fernando Manuel Diamantino, Costa José Carlos Teixeira da, Queiroz Mário Fernando Oliveira Viana de

机构信息

Serviço de reumatologia e doenças ósseas metabólicas, Hospital de Santa Maria, Lisboa, Portugal.

出版信息

Rev Bras Reumatol. 2004 Apr;44(2):129-38. doi: 10.1590/s0482-50042004000200005.

Abstract

OBJECTIVE

to characterize the exocrine and non-exocrine clinical disease manifestations of 74 patients with primary Sjögren's Syndrome (pSS).

METHODS

retrospective study of pSS patients according to the new 2002 American-European criteria, followed in the Hospital Santa Maria, Rheumatology Outpatient Clinics, in the last 25 years (mean follow-up of 7.7 years).

RESULTS

all patients presented surface exocrine disease, especially xerostomia and keratoconjunctivitis sicca. Internal organ exocrine disease was found in 25 patients (33.8%), whilst only one patient (1.4%) developed monoclonal B lymphocyte disease (pulmonary pseudolymphoma). Fifty-five patients (74.3%) also displayed non-exocrine manifestations, in particular inflammatory mediator-induced disease (68.9%). Inflammatory vascular disease was present in 54% of patients and noninflammatory vascular disease in 27%. Autoimmune thyroiditis was found in 5 patients (6.8%).

CONCLUSIONS

the disease is dominated by oral and ocular involvement, while severe organic manifestations are less frequent. This classification model allows a comparison of patients with physiopathological abnormalities and offers the possibility of finding markers of activity/cronicity related to them.

摘要

目的

描述74例原发性干燥综合征(pSS)患者的外分泌和非外分泌临床疾病表现。

方法

根据新的2002年欧美标准对pSS患者进行回顾性研究,这些患者在过去25年中于圣玛丽亚医院风湿病门诊就诊(平均随访7.7年)。

结果

所有患者均出现体表外分泌疾病,尤其是口干和干燥性角结膜炎。25例患者(33.8%)发现内脏器官外分泌疾病,而仅有1例患者(1.4%)发生单克隆B淋巴细胞疾病(肺假性淋巴瘤)。55例患者(74.3%)还表现出非外分泌表现,特别是炎症介质诱导的疾病(68.9%)。54%的患者存在炎症性血管疾病,27%的患者存在非炎症性血管疾病。5例患者(6.8%)发现自身免疫性甲状腺炎。

结论

该疾病以口腔和眼部受累为主,而严重的器官表现较少见。这种分类模型允许对具有生理病理异常的患者进行比较,并提供了寻找与其相关的活动/慢性标志物的可能性。

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