Strimlan C V, Rosenow E C, Divertie M B, Harrison E G
Chest. 1976 Sep;70(03):354-61. doi: 10.1378/chest.70.3.354.
A review of 343 patients with classic Sjogren's syndrome seen at the Mayo Clinic from 1967 through 1974 revealed pulmonary involvement in 31 patients (9 percent). Cough dyspnea, recurrent pneumonitis, and pleuritic pain were the primary complaints. Chest roentgenographic features included diffuse interstitial patterns, diffuse alveolar patterns, and pleural effusions. Laboratory studies revealed hypergammaglobulinemia in 16 of 22 patients tested, and 23 of the 31 patients had positive tests for anti-nuclear antibody, rheumatoid factor, or lupus erythematosus cells. Pulmonary function tests showed a restrictive ventilatory impairment or low diffusion capacity (or both in all 18 patients studied. Pathologic diagnosis included the full range of pulmonary lesions described in Sjogren's syndrome syndrome, ie, lymphocytic interstitial pneumonitis, pseudolymphoma, malignant lymphoma, diffuse interstitial pulmonary fibrosis, and bronchopneumonia. The clinical pulmonary diagnosis included diffuse interstitial fibrosis, recurrent pneumonitis, pleural effusions, and suspected lymphoma or pseudolymphoma. We conclude that pulmonary lesions occur in Sjogren's syndrome more frequently than previously reported.
一项对1967年至1974年在梅奥诊所就诊的343例经典干燥综合征患者的回顾显示,31例(9%)患者出现肺部受累。咳嗽、呼吸困难、反复肺炎和胸膜炎性疼痛是主要症状。胸部X线特征包括弥漫性间质模式、弥漫性肺泡模式和胸腔积液。实验室研究显示,在22例接受检测的患者中,16例出现高球蛋白血症,31例患者中有23例抗核抗体、类风湿因子或红斑狼疮细胞检测呈阳性。肺功能测试显示,所有18例接受研究的患者均存在限制性通气功能障碍或低弥散能力(或两者兼有)。病理诊断包括干燥综合征中描述的全范围肺部病变,即淋巴细胞间质性肺炎、假性淋巴瘤、恶性淋巴瘤、弥漫性间质性肺纤维化和支气管肺炎。临床肺部诊断包括弥漫性间质性纤维化、反复肺炎、胸腔积液以及疑似淋巴瘤或假性淋巴瘤。我们得出结论,干燥综合征中肺部病变的发生率比以前报道的更高。