Repository logo
  • English
  • 中文
Log In
Have you forgotten your password?
  1. Home
  2. College of Medicine / 醫學院
  3. School of Medicine / 醫學系
  4. Clinical Presentations, Laboratory Results and Outcomes of Patients with Kikuchi's Disease: Emphasis on the Association Between Recurrent Kikuchi's Disease and Autoimmune Diseases
 
  • Details

Clinical Presentations, Laboratory Results and Outcomes of Patients with Kikuchi's Disease: Emphasis on the Association Between Recurrent Kikuchi's Disease and Autoimmune Diseases

Journal
Journal of Microbiology, Immunology and Infection
Journal Volume
43
Journal Issue
5
Pages
366-371
Date Issued
2010
Author(s)
Cheng C.-Y.
WANG-HUEI SHENG  
Lo Y.-C.
Chung C.-S.
YEE-CHUN CHEN  
SHAN-CHWEN CHANG  
DOI
10.1016/S1684-1182(10)60058-8
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-78049383899&doi=10.1016%2fS1684-1182%2810%2960058-8&partnerID=40&md5=b398633dddcc0b5359962f3bff3bdd3c
https://scholars.lib.ntu.edu.tw/handle/123456789/536100
Abstract
Background/Purpose: Kikuchi's disease (KD), also known as histiocytic necrotizing lymphadenitis, is a benign and self-limiting disease of unknown etiology that mainly affects young women. There is limited data on the long-term prognosis of patients with KD. Methods: We describe the clinical manifestations and outcomes of 195 patients, diagnosed as having KD at National Taiwan University Hospital from March 1989 to September 2006. Results: All together, 53.3% of our patients presented with tender lymphadenopathy, 37.9% with fever and 16.9% with headache. The most common laboratory findings were elevated erythrocyte sedimentation rate (78.9%), elevated serum lactate dehydrogenase (52.5%), elevated C-reactive protein (38.3%), monocytosis (26.9%), elevated serum alanine aminotransferase (23.3%) and leukopenia (18.9%). A total of 183 patients followed a benign course, with spontaneous resolution of fever and lymphadenopathy. However, 14 patients (14.6%) with follow-up of more than 6 months had clinical recurrence of KD; hence, long-term follow-up is suggested. Five of these patients developed an autoimmune disease, namely, systemic lupus erythematosus (n = 2), Graves' disease (n = 2), or mixed connective tissue disease (n = 1). One patient with recurrent KD died of intracranial hemorrhage due to thrombocytopenia. Conclusion: The prognosis for KD patients is generally optimistic; however, a concurrent autoimmune disease or the risk of developing an autoimmune disease requires careful monitoring. ? 2010 Taiwan Society of Microbiology.
SDGs

[SDGs]SDG3

Other Subjects
alanine aminotransferase; antibiotic agent; C reactive protein; lactate dehydrogenase; nonsteroid antiinflammatory agent; paracetamol; steroid; adolescent; adult; alanine aminotransferase blood level; antibiotic therapy; arthralgia; article; autoimmune disease; brain hemorrhage; child; chill; clinical feature; coughing; disease association; disease course; epigastric pain; erythrocyte sedimentation rate; female; fever; follow up; Graves disease; headache; human; human tissue; Kikuchi disease; laboratory test; lactate dehydrogenase blood level; leukopenia; long term care; lymph node biopsy; lymphadenopathy; major clinical study; malaise; male; mixed connective tissue disease; monocytosis; night sweat; preschool child; prognosis; rash; recurrent disease; rhinorrhea; school child; sore throat; steroid therapy; systemic lupus erythematosus; thrombocytopenia; university hospital; upper respiratory tract infection; weight reduction; Adolescent; Adult; Autoantibodies; Autoimmune Diseases; Child; Female; Fever; Follow-Up Studies; Histiocytic Necrotizing Lymphadenitis; Humans; Lymphatic Diseases; Male; Middle Aged; Prognosis; Recurrence; Retrospective Studies; Taiwan; Treatment Outcome; Young Adult
Type
journal article

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

總館學科館員 (Main Library)
醫學圖書館學科館員 (Medical Library)
社會科學院辜振甫紀念圖書館學科館員 (Social Sciences Library)

開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

  • 請確認所上傳的全文是原創的內容,若該文件包含部分內容的版權非匯入者所有,或由第三方贊助與合作完成,請確認該版權所有者及第三方同意提供此授權。
    Please represent that the submission is your original work, and that you have the right to grant the rights to upload.
  • 若欲上傳已出版的全文電子檔,可使用Open policy finder網站查詢,以確認出版單位之版權政策。
    Please use Open policy finder to find a summary of permissions that are normally given as part of each publisher's copyright transfer agreement.
  • 網站簡介 (Quickstart Guide)
  • 使用手冊 (Instruction Manual)
  • 線上預約服務 (Booking Service)
  • 方案一:臺灣大學計算機中心帳號登入
    (With C&INC Email Account)
  • 方案二:ORCID帳號登入 (With ORCID)
  • 方案一:定期更新ORCID者,以ID匯入 (Search for identifier (ORCID))
  • 方案二:自行建檔 (Default mode Submission)
  • 方案三:學科館員協助匯入 (Email worklist to subject librarians)

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science