지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2018.1
- 수록면
- 207 - 211 (5page)
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초록· 키워드
오류제보하기
Idiopathic hypereosinophilic syndrome (IHES) is a rare disease that is characterized by otherwise unexplained persistent eosinophilia and organ damage caused by eosinophilic infiltration. Its manifestations are highly variable but clinically apparent arthritis is uncommonly observed. Although Korean cases of severe eosinophilia in patients with rheumatoid arthritis (RA) or IHES concurrent with RA have been published, there are no reports of IHES with joint involvement. This paper reports a case of IHES presenting with persistent peripheral eosinophilia, fever, skin rash, multiple lymphadenopathy, and polyarthritis, including the distal interphalangeal joints of the hands.
목차
등록된 정보가 없습니다.
참고문헌 (15)
참고문헌 신청
Curtis C / 2016 / Hypereosinophilic Syndrome / Clin Rev Allergy Immunol 50:240~251
Weller PF / 1994 / The idiopathic hypereosinophilic syndrome / Blood 83:2759~2779
Brogadir SP / 1980 / A hypereosinophilic syndrome mimicking rheumatoid arthritis / Am J Med 69:799~802
Spry CJ / 1983 / Clinical features of fifteen patients with the hypereosinophilic syndrome / Q J Med 52:1~22
Martin-Santos JM / 1988 / Arthritis in idiopathic hypereosinophilic syndrome / Arthritis Rheum 31:120~125
Weller PF / 1994 / The idiopathic hypereosinophilic syndrome / Blood 83:2759~2779
Brogadir SP / 1980 / A hypereosinophilic syndrome mimicking rheumatoid arthritis / Am J Med 69:799~802
Spry CJ / 1983 / Clinical features of fifteen patients with the hypereosinophilic syndrome / Q J Med 52:1~22
Martin-Santos JM / 1988 / Arthritis in idiopathic hypereosinophilic syndrome / Arthritis Rheum 31:120~125
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