A case of primary Sjogren's syndrome with pulmonary-limited Wegener's granulomatosis

被引:7
|
作者
Yazisiz, Veli [1 ,2 ]
Ozbudak, Irem Hicran [3 ]
Nizam, Ilknur [4 ]
Erbasan, Funda [2 ]
Avci, Ali Berkant [2 ]
Ozbudak, Omer [5 ]
Terzioglu, Ender [2 ]
机构
[1] Akdeniz Univ, Tip Fak, Ic Hastaliklari AD, TR-07058 Antalya, Turkey
[2] Akdeniz Univ, Dept Internal Med, Div Rheumatol & Immunol, TR-07058 Antalya, Turkey
[3] Akdeniz Univ, Dept Pathol, TR-07058 Antalya, Turkey
[4] Akdeniz Univ, Dept Internal Med, TR-07058 Antalya, Turkey
[5] Akdeniz Univ, Dept Resp Med, TR-07058 Antalya, Turkey
关键词
Antineutrophil cytoplasmic antibody (ANCA); Sjogren's syndrome; Wegener's granulomatosis; ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES; CLASSIFICATION; PREVALENCE; DISEASE;
D O I
10.1007/s00296-009-1045-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A 60-year-old woman had a history of dyspnea for 5-6 weeks. The chest radiograph and computed tomography scans revealed bilateral patchy reticulonodular pattern. The patient had positive test results for antineutrophil cytoplasmic antibody against proteinase-3 (c-ANCA), antinuclear antibody and anti-Ro antibody. According to European Study Group on Classification Criteria for Sjogren's Syndrome, the patient was diagnosed as primary Sjogren's syndrome based on the presence of clinical features, positive findings on Schirmer's test and parotis scintigraphy. Lung biopsy obtained by wedge resection showed granulomatous inflammation with extensive multinuclear giant cells involving the lung parenchyma and vascular structures. There was neither upper airway nor renal involvement. Thus, the patient was simultaneously diagnosed as pulmonary-limited Wegener's granulomatosis. With this unique case, we would like to emphasize that the awareness of ANCA-associated vasculitis as a diagnostic possibility in primary Sjogren's syndrome is important during the work-up of lung lesions.
引用
收藏
页码:1235 / 1238
页数:4
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