論文

査読有り
2011年4月

Hyperviscosity syndrome associated with systemic plasmacytosis

CLINICAL AND EXPERIMENTAL DERMATOLOGY
  • S. Noda
  • ,
  • Y. Tsunemi
  • ,
  • Y. Ichimura
  • ,
  • A. Miyamoto
  • ,
  • Z. Tamaki
  • ,
  • T. Takekoshi
  • ,
  • Y. Asano
  • ,
  • T. Hoashi
  • ,
  • M. Sugaya
  • ,
  • T. Inoue
  • ,
  • S. Sato

36
3
開始ページ
273
終了ページ
276
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1111/j.1365-2230.2010.03928.x
出版者・発行元
WILEY-BLACKWELL

P>Systemic plasmacytosis is characterized by plasma cell proliferation in multiple organs including skin, and by polyclonal hypergammaglobulinaemia. Hyperviscosity-related retinopathy has never been described with this condition, to our knowledge. We report a case of systemic plasmacytosis in a 49-year-old Japanese woman, who presented with fever, multiple erythematous plaques, hypergammaglobulinaemia, renal failure and bilateral retinal haemorrhage. Reduction of immunoglobulin with oral steroid reversed the retinopathy related to hyperviscosity syndrome. When marked hypergammaglobulinaemia is found in a patient with systemic plasmacytosis, funduscopic examination should be performed to reveal early asymptomatic retinal changes, because the retinopathy is treatable by control of the underlying disease.

Web of Science ® 被引用回数 : 2

リンク情報
DOI
https://doi.org/10.1111/j.1365-2230.2010.03928.x
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000288664200009&DestApp=WOS_CPL

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