Soden M, Tempany E, Bresnihan B
Department of Rheumatology, St Vincent's Hospital, Dublin, Ireland.
Br J Rheumatol. 1989 Aug;28(4):341-3. doi: 10.1093/rheumatology/28.4.341.
An 8-year-old boy with cystic fibrosis presented with a chronic polyarthritis. Histological examination of the synovium demonstrated multiple non-caseating granulomata. A systematic search for sarcoidosis revealed characteristic ophthalmic abnormalities and an elevated serum level of angiotensin converting enzyme. An association between cystic fibrosis and sarcoidosis is likely.
一名患有囊性纤维化的8岁男孩出现慢性多关节炎。滑膜组织学检查显示多个非干酪样肉芽肿。对结节病进行系统检查发现有特征性眼部异常及血清血管紧张素转换酶水平升高。囊性纤维化与结节病之间可能存在关联。