Takata T, Nagafuchi S, Tsuda H, Uehira K, Kondo S, Ueda A, Ishii H, Niho Y
First Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Jpn J Med. 1991 Jan-Feb;30(1):92-6. doi: 10.2169/internalmedicine1962.30.92.
A 62-year-old Japanese female was admitted due to dyspnea. She showed a marked increase in CA19-9 (maximum, 192,000 U/ml) and monoclonal IgM-kappa type rheumatoid factor (RF) activity. The patient died of respiratory failure 3 months later. Autopsy findings revealed an infiltration of IgM-kappa-positive plasma cells in the pulmonary interstitium, and therefore a diagnosis of lymphoid interstitial pneumonia (LIP) was made. The bronchoepithelial cells were stained with monoclonal antibody-reactive with CA 19-9 antigen. This is the first documented LIP, associated with a marked increase in monoclonal IgM-kappa type RF and CA19-9 in the serum.
一名62岁的日本女性因呼吸困难入院。她的CA19-9显著升高(最高达192,000 U/ml),且单克隆IgM-κ型类风湿因子(RF)活性增强。患者3个月后死于呼吸衰竭。尸检结果显示肺间质中有IgM-κ阳性浆细胞浸润,因此诊断为淋巴样间质性肺炎(LIP)。支气管上皮细胞被与CA 19-9抗原反应的单克隆抗体染色。这是首例有文献记载的LIP,伴有血清中单克隆IgM-κ型RF和CA19-9显著升高。