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原发性干燥综合征(primary Sj(?)gren’s syndro-me,PSS)的肺累及较常见,可表现为胸膜炎、间质纤维化等。作者报告36例 PSS 的呼吸系统表现。36例中男3、女33例,年龄33～80(平均52.5)岁。在呼吸系检查前,发病已1～20(平均5.9)年。PSS 的诊断根据口腔干燥、干性角膜结膜炎以及在较小的唾液腺有局灶性淋巴细胞浸润。19例(52%)有腺体外的表现如雷诺氏现象、脾肿大、淋巴结肿
Primary Sj (?) Gren’s syndro-me, PSS) lung involvement more common, can be expressed as pleurisy, interstitial fibrosis and so on. The authors report respiratory performance in 36 patients with PSS. 36 cases of male 3, female 33 cases, aged 33 to 80 (average 52.5) years old. In the respiratory examination, the incidence has been 1 to 20 (average 5.9) years. The diagnosis of PSS is based on dry mouth, dry keratoconjunctivitis, and focal lymphocytic infiltrates in the smaller salivary glands. Nineteen (52%) had extrarenal manifestations of Raynaud’s phenomenon, splenomegaly, and swollen lymph nodes