論文

査読有り 国際誌
2021年6月

Inducible skin‐associated lymphoid tissue (iSALT) in a patient with Schnitzler syndrome who manifested wheals on recurrent localized erythema

British Journal of Dermatology
  • H. Kamido
  • ,
  • D. Shimomiya
  • ,
  • T. Kogame
  • ,
  • R. Takimoto‐Ito
  • ,
  • T.R. Kataoka
  • ,
  • M. Hirata
  • ,
  • C. Ueshima
  • ,
  • A. Otsuka
  • ,
  • F.M. Ghazawi
  • ,
  • T. Nomura
  • ,
  • N. Kambe
  • ,
  • K. Kabashima

184
6
開始ページ
1199
終了ページ
1201
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1111/bjd.19808
出版者・発行元
Wiley

Schnitzler syndrome is characterized by a chronic urticarial rash with an intermittent fever, and is considered to be an acquired form of autoinflammatory syndrome because its clinical phenotypes are similar to cryopyrin-associated periodic syndrome with a gain-of-function mutation in NLRP3.1 Patients with Schnitzler syndrome also exhibit IgM monoclonal gammopathy, and 15-20% of patients eventually develop a lymphoproliferative disorder resembling Waldenström macroglobulinemia with an MYD88 mutation.2 At present, the precise pathogenesis of Schnitzler syndrome remains unknown.

リンク情報
DOI
https://doi.org/10.1111/bjd.19808
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/33445206
URL
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjd.19808
URL
https://onlinelibrary.wiley.com/doi/full-xml/10.1111/bjd.19808
ID情報
  • DOI : 10.1111/bjd.19808
  • ISSN : 0007-0963
  • eISSN : 1365-2133
  • PubMed ID : 33445206

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