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。

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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。

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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。

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Moreover, in the last few weeks, Iressa has been linked to 39 deaths in Japan from interstitial pneumonia, a rare lung disorder.

FORBES: Genta Chief Defends FDA