MISC

1999年9月

Intravascular lymphomatosis presenting as an ascending cauda equina: conus medullaris syndrome: remission after biweekly CHOP therapy

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
  • T Nakahara
  • ,
  • T Saito
  • ,
  • A Muroi
  • ,
  • Y Sugiura
  • ,
  • M Ogata
  • ,
  • Y Sugiyama
  • ,
  • T Yamamoto

67
3
開始ページ
403
終了ページ
406
記述言語
英語
掲載種別
出版者・発行元
BRITISH MED JOURNAL PUBL GROUP

A 63 year old man developed dysaesthesia in the legs followed by a subacute ascending flaccid paraparesis with sacral sensory and autonomic involvement. Intravascular lymphomatosis (IVL) was favoured by the presence of low grade fever and raised serum C reactive protein, CSF pleocytosis, raised lymphoma markers (serum LDH, soluble IL-2 receptor), and steroid responsiveness. Only muscle, among several organ biopsies, confirmed IVL. A cytogenetic study of the bone marrow showed chromosome 6 monosomy, as previously reported. The monosomy of chromosome 19, which bears the intercellular cell adhesion molecule-1, newly found in this case, may be related to the unique tumour embolisation of IVL. The CHOP regimen (six courses in 12 weeks) using granulocyte colony stimulating factor (G-CSF) led to gradual resolution of myeloradiculopathy and laboratory supported remission lasting for more than 13 months. The biweekly CHOP with G-CSF support may be a choice of chemotherapy in averting rapidly fatal IVL.

リンク情報
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000082195200027&DestApp=WOS_CPL
ID情報
  • ISSN : 0022-3050
  • Web of Science ID : WOS:000082195200027

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