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An early and non-invasive diagnosis of histiocytic necrotizing lymphadenitis

Research Project

Project/Area Number 25860868
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Pediatrics
Research InstitutionKyushu University

Principal Investigator

MASATAKA Ishimura  九州大学, 医学(系)研究科(研究院), 助教 (10448417)

Project Period (FY) 2013-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywords組織球性壊死性リンパ節炎 / 菊池病 / 早期診断 / インターフェロン / インターフェロン誘導遺伝子 / 自己炎症性疾患 / 壊死性リンパ節炎 / 迅速診断 / 定量PCR
Outline of Final Research Achievements

Histiocytic necrotizing lymphadenitis (HNL), also called Kikuchi-Fujimoto disease, is a benign, self-limiting inflammatory disease with fever and painful cervical lymphadenopathy of unknown etiology. A lymph node biopsy is required for the definitive diagnosis because of no specific symptoms or laboratory findings for HNL. We investigated genes specifically expressed in the patients by analyzing whole transcriptome using microarray analysis of peripheral blood mononuclear cells (PBMC). The expression levels of the up-regulated genes by microarray were verified by quantitative PCR. H The discriminant analysis using the expression levels of these five genes distinguished HNL with 84 % accuracy. An analysis of the gene expression profile of PBMC may provide a rapid non-invasive diagnosis.

Report

(3 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • Research Products

    (9 results)

All 2015 2014 2013

All Journal Article (6 results) (of which Peer Reviewed: 6 results,  Open Access: 1 results,  Acknowledgement Compliant: 2 results) Presentation (2 results) Book (1 results)

  • [Journal Article] Wiskott-Aldrich syndrome in a girl caused by heterozygous WASP mutation and extremely skewed X-chromosome inactivation: a novel association with maternal uniparental isodisomy 62015

    • Author(s)
      Takimoto T, Takada H, Ishimura M, Kirino M, Hata K, Ohara O, Morio T, Hara T
    • Journal Title

      Neonatology

      Volume: 107 Issue: 3 Pages: 185-190

    • DOI

      10.1159/000370059

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Early progression of atherosclerosis in children with chronic infantile neurological cutaneous and articular syndrome2014

    • Author(s)
      Yamamura K, Takada H, Uike K, Nakashima Y, Hirata Y, Nagata H, Takimoto T, Ishimura M, Morihana E, Ohga S, Hara T
    • Journal Title

      Rheumatology

      Volume: 53 Issue: 10 Pages: 1783-1787

    • DOI

      10.1093/rheumatology/keu180

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Journal Article] A Non-invasive Diagnosis of Histiocytic Necrotizing Lymphadenitis by Means of Gene Expression Profile Analysis of Peripheral Blood Mononuclear Cells2013

    • Author(s)
      Masataka Ishimura, Hiroyuki Yamamoto, Yumi Mizuno, Hidetoshi Takada, Motohiro Goto, Takehiko Doi, Takayuki Hoshina, Shouichi Ohga, Koichi Ohshima, and Toshiro Hara
    • Journal Title

      Journal of Clinical immunology

      Volume: 33 Pages: 1018-1026

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] Long-term liposteroid therapy for idiopathic pulmonary hemosiderosis2013

    • Author(s)
      Doi T, Ohga S, Ishimura M, Takada H, Ishii K, Ihara K, Nagai H, Hara T
    • Journal Title

      Eur J Pediatr

      Volume: 172 Issue: 11 Pages: 1475-1478

    • DOI

      10.1007/s00431-013-2065-9

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] Paediatric presentation and outcome of congenital protein C deficiency in Japan.2013

    • Author(s)
      Ohga S, Kang D, Kinjo T, Ochiai M, Doi T, Ishimura M, Kayamori Y, Urata M, Yamamoto J, Suenobu SI, Kanegane H, Ikenoue T, Shirahata A, Hara T.
    • Journal Title

      Haemophilia

      Volume: 19 Issue: 3 Pages: 378-384

    • DOI

      10.1111/hae.12097

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] The identification of a novel splicing mutation in C1qB in a Japanese family with C1q deficiency: a case report2013

    • Author(s)
      Higuchi Y, Shimizu J, Hatanaka M, Kitano E, Kitamura H, Takada H, Ishimura M, Hara T, Ohara O, Asagoe K, Kubo T
    • Journal Title

      Pediatr Rheumatol Online J

      Volume: 28 Issue: 1 Pages: 41-41

    • DOI

      10.1186/1546-0096-11-41

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Presentation] An Early and Non-invasive Diagnostic Method for Histiocytic Necrotizing Lymphadenitis2014

    • Author(s)
      Ishimura M., Mizuno Y., Takada H., Ohga S., Hara T.
    • Organizer
      FISP/M
    • Place of Presentation
      Fukuoka
    • Year and Date
      2014-08-30
    • Related Report
      2014 Annual Research Report
  • [Presentation] A Non-invasive Diagnosis ofHistiocytic Necrotizing Lymphadenitis2013

    • Author(s)
      T. Hara, M. Ishimura, H. Yamamoto, Y. Mizuno, H. Takada, K. Ohshima
    • Organizer
      FRONTIERS IN IMMUNOLOGY RESEARCH NETWORK
    • Place of Presentation
      MONTE CARLO, MONACO
    • Related Report
      2013 Research-status Report
  • [Book] 小児内科2014

    • Author(s)
      石村匡崇、高田英俊、原寿郎
    • Total Pages
      5
    • Publisher
      東京医学社
    • Related Report
      2014 Annual Research Report

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Published: 2014-07-25   Modified: 2019-07-29  

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