http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
- 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
- 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
RISS 인기검색어
- 검색키워드
- 저자 : ( Homas V Colby ) (검색결과 1 건)
- 무료
- 기관 내 무료
- 유료
-
김호철,지원준,김미영,장세진,이창근,한승봉,( Homas V Colby ),김동순 대한결핵 및 호흡기학회 2013 대한결핵 및 호흡기학회 추계학술대회 초록집 Vol.116 No.-
Introduction: Undifferentiated connective tissue disease (UCTD) defined as conditions characterised by the presence of signs and symptoms suggestive of connective tissue disease (CTD) with autoantibody but do not fulfill classification criteria of specific CTD. Although NSIP pattern was first described in UCTD, UIP pattern seems to be not infrequent, and then the differentiation from idiopathic pulmonary fibrosis may be difficult. The aim of this study was to investigate the frequency and prognosis of UIP and NSIP pattern in UCTD and prognostic difference between UCTD-UIP and IPF. Methods: The medical records including rheumatologic symptoms and serologic test for autoantibody of 788 patients diagnosed as IIP from January 2005 to December 2012 at AMC were retrospectively reviewed. UCTD was diagnosed according to narrow criteria and the prognosis was compared between UCTD-UIP and UCTD-NSIP and also between UCTD-UIP and IPF. Results: Total 105 patients (13.3%) diagnosed as UCTD and 44 patients had UIP pattern and 29 patients had NSIP pattern, 8 OP patterns and the pathologic pattern was not specified in remaining 24 patients. Overall survival of UCTD-UIP group was shorter than UCTD-NSIP group (p=0.021) but significantly better than that of IPF group(p=0.042). Definite CTD developed in 2.9% (3/105) of patients during follow-up days. Conclusion: UIP pattern is frequent in UCTD related interstitial pneumonia and the prognosis was worse than UCTD-NSIP. However, the prognosis of UCTD-UIP was better than IPF, it is important to search for UCTD in suspected IPF.Introduction: Undifferentiated connective tissue disease (UCTD) defined as conditions characterised by the presence of signs and symptoms suggestive of connective tissue disease (CTD) with autoantibody but do not fulfill classification criteria of specific CTD. Although NSIP pattern was first described in UCTD, UIP pattern seems to be not infrequent, and then the differentiation from idiopathic pulmonary fibrosis may be difficult. The aim of this study was to investigate the frequency and prognosis of UIP and NSIP pattern in UCTD and prognostic difference between UCTD-UIP and IPF. Methods: The medical records including rheumatologic symptoms and serologic test for autoantibody of 788 patients diagnosed as IIP from January 2005 to December 2012 at AMC were retrospectively reviewed. UCTD was diagnosed according to narrow criteria and the prognosis was compared between UCTD-UIP and UCTD-NSIP and also between UCTD-UIP and IPF. Results: Total 105 patients (13.3%) diagnosed as UCTD and 44 patients had UIP pattern and 29 patients had NSIP pattern, 8 OP patterns and the pathologic pattern was not specified in remaining 24 patients. Overall survival of UCTD-UIP group was shorter than UCTD-NSIP group (p=0.021) but significantly better than that of IPF group(p=0.042). Definite CTD developed in 2.9% (3/105) of patients during follow-up days. Conclusion: UIP pattern is frequent in UCTD related interstitial pneumonia and the prognosis was worse than UCTD-NSIP. However, the prognosis of UCTD-UIP was better than IPF, it is important to search for UCTD in suspected IPF.
연관 검색어 추천
이 검색어로 많이 본 자료
활용도 높은 자료
