1·Most collagen-vascular diseases can cause chronic interstitial pneumonia with clinical, radiologic, HRCT, and pathologic features indistinguishable from those of IPF.
大部分胶原血管病在临床上会出现慢性间质性肺炎，无论平片、HRCT还是病理均无法于IPF鉴别。
2·Methods Serial imaging materials of 7 cases of acute interstitial pneumonia proved by open-lung biopsy or clinical comprehensive diagnosis were retrospectively analyzed.
方法：回顾分析经开胸肺活检证实或临床综合诊断7例急性间质性肺炎的系列影像资料。
3·Methods a retrospective analysis of 23 patients after Kidney transplantation with HCMV interstitial pneumonia was undertaken to summarize its clinical features and therapy.
方法通过对23例肾脏移植术后HCMV间质性肺炎患者进行回顾性分析，总结其临床特点和治疗措施。
4·Staining and observing shows that the most pathological changes were interstitial pneumonia and hemorrhagic pneumonia, typical nonsuppurative encephalitis, and neurogangliitis et al.
染色观察显示，病理组织学变化主要表现为间质性肺炎和出血性肺炎、典型的非化脓性脑炎、神经节炎等；
5·Conclusions GIP is a very rare chronic interstitial pneumonia, and has no characteristic clinical manifestations. Radiographic findings are similar to other idiopathic interstitial pneumonias.
结论GIP是非常罕见的慢性间质性肺炎，无特异性的临床表现，影像学表现类似于特发性间质性肺炎。
6·The histopathological results showed the interstitial pneumonia in the immunized rabbits which were similar with that of SARS patients, but no other significant changes were found in other tissues.
免疫后，兔肺组织出现病毒间质性肺炎病理变化，与SARS患者肺部病理变化相似，其它组织没有明显的病理变化。