Ishii Hiroshi, Iwata Atsuko, Sakamoto Noriho, Mizunoe Shunji, Mukae Hiroshi, Kadota Jun-ichi
Department of Internal Medicine II, Oita University Faculty of Medicine, Yufu.
Intern Med. 2009;48(10):827-30. doi: 10.2169/internalmedicine.48.1876. Epub 2009 May 15.
Desquamative interstitial pneumonia (DIP) is a rare pattern of diffuse parenchymal lung disease known as one of the idiopathic interstitial pneumonias and is considered to be a smoking- or dust inhalation-related interstitial pneumonia in the majority of cases. This report presents the first case of DIP in which the pulmonary manifestation preceded the onset of rheumatoid arthritis. This case and our review of twenty-four DIP cases (nineteen cases previously-reported from Japan, plus five cases in our departments) indicate the possibility that the DIP pattern is an additional form of diffuse interstitial pneumonia that may develop in association with autoimmune diseases.
脱屑性间质性肺炎(DIP)是一种罕见的弥漫性实质性肺疾病模式,是特发性间质性肺炎之一,在大多数病例中被认为是与吸烟或吸入粉尘相关的间质性肺炎。本报告介绍了首例脱屑性间质性肺炎病例,该病例中肺部表现先于类风湿性关节炎发作。该病例以及我们对24例脱屑性间质性肺炎病例(19例先前来自日本的报告病例,加上我们科室的5例病例)的回顾表明,脱屑性间质性肺炎模式可能是一种与自身免疫性疾病相关的弥漫性间质性肺炎的额外形式。