Kirsten D, Glombitza J, Ebner S, Ehrhardt G
Zentralklinik für Herz- und Lungenkrankheiten Bad Berka, DDR.
Pneumologie. 1990 Aug;44(8):970-2.
This is a case report on a 66-year old woman who suffered from chronic polyarthritis for 15 years and developed a sicca syndrome pattern for 2 years. 2 years later epithelioid cell granulomas were found from a submandibular lymph node as well as from a suspicious area at the epiglottis and the mucosa of the upper lip. Moreover, there was a chronic keratoconjunctivitis and discrete lung involvement. The sarcoidosis on the lip and at the epiglottis disappeared, and lung involvement and conjunctivitis improved under corticosteroid therapy. In spite of above therapy, the sicca syndrome pattern and the rheumatic complaints (osteoporosis) persisted.
这是一份关于一名66岁女性的病例报告，该女性患有慢性多关节炎15年，出现干燥综合征症状2年。2年后，在颌下淋巴结以及会厌和上唇黏膜的可疑区域发现上皮样细胞肉芽肿。此外，还有慢性角结膜炎和肺部散在受累。唇部和会厌的结节病消失，肺部受累和结膜炎在皮质类固醇治疗下有所改善。尽管进行了上述治疗，干燥综合征症状和风湿性症状（骨质疏松）仍持续存在。
