Hughes M, Fox H
J Clin Pathol. 1972 Sep;25(9):817-20. doi: 10.1136/jcp.25.9.817.
A study has been made of 33 cases of granulomatous hepatitis. Of these, 12 were eventually established as cases of sarcoidosis, nine as cases of tuberculosis, and four as examples of primary biliary cirrhosis. No clinical diagnosis was ever reached in six cases. Analysis of the histological features of these cases shows that the presence of caseation or of tubercle bacilli will only allow for the diagnosis of approximately 50% of cases of tuberculosis. Histological features which are suggestive of tuberculosis are a paucity of granulomata, a scantiness of giant cells, a relatively mild surrounding chronic inflammatory cell infiltrate, and an absence of reticulin. The granulomata are more likely to be due to sarcoidosis if they are numerous, contain many giant cells, are confined to the portal areas, and show a well marked surrounding non-specific chronic inflammatory cell infiltrate. Histological features of cases in which no clinical diagnosis was reached suggest that they are more likely to be due to sarcoidosis than to tuberculosis.
对33例肉芽肿性肝炎病例进行了研究。其中,12例最终确诊为结节病,9例为结核病,4例为原发性胆汁性肝硬化。6例从未得出临床诊断。对这些病例的组织学特征分析表明,干酪样坏死或结核杆菌的存在仅能诊断约50%的结核病例。提示结核病的组织学特征为肉芽肿数量少、巨细胞稀少、周围慢性炎症细胞浸润相对较轻以及无网状纤维。如果肉芽肿数量多、含有许多巨细胞、局限于门管区且周围有明显的非特异性慢性炎症细胞浸润,则更可能是结节病所致。未得出临床诊断的病例的组织学特征表明,它们更可能是结节病而非结核病所致。