Prefaut C, Kienlen J, Lloret M C, Chardon G, du Cailar J
Poumon Coeur. 1977;33(6):391-4.
Twenty patients having previously had a Mendelson's syndrome were subjected to a respiratory functional test. A syndrome of diffuse interstitial pulmonary fibrosis (DIPF) was found only in 3 cases examined shortly after the pneumopathy. In one of these cases, another examination done later showed signs of regressing fibrosis. The authors concluded that if a functional syndrome of DIPF occurred immediately after a Mendelson's pneumopathy, it eventually disappeared in the long term in most cases.
20名曾患门德尔松综合征的患者接受了呼吸功能测试。仅在肺炎后不久接受检查的3例患者中发现了弥漫性间质性肺纤维化(DIPF)综合征。其中1例患者后来进行的另一项检查显示纤维化有消退迹象。作者得出结论,如果在门德尔松肺炎后立即出现DIPF功能综合征,那么在大多数情况下,从长远来看它最终会消失。