Motor neuron disease, lymphoproliferative disease, and bone marrow biopsy
Some have suggested that nonfamilial motor neuron disease (MND) may be autoimmune, and the neurological disorder may benefit from immunotherapy. There have been reports of over 30 cases of lymphoproliferative disease (lymphoma, multiple myeloma, Waldenström's macroglobulinemia) with MND, and th...
Saved in:
Published in | Muscle & nerve Vol. 19; no. 10; pp. 1334 - 1337 |
---|---|
Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
John Wiley & Sons, Inc
01.10.1996
Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 0148-639X 1097-4598 |
DOI | 10.1002/(SICI)1097-4598(199610)19:10<1334::AID-MUS11>3.0.CO;2-U |
Cover
Summary: | Some have suggested that nonfamilial motor neuron disease (MND) may be autoimmune, and the neurological disorder may benefit from immunotherapy. There have been reports of over 30 cases of lymphoproliferative disease (lymphoma, multiple myeloma, Waldenström's macroglobulinemia) with MND, and these patients might be offered immunosuppressive therapy. Bone marrow examination might increase the sensitivity of the diagnostic workup for lymphoma and other lymphoproliferative disorders. We examined the bone marrow in our first evaluation of 161 patients with MND seen at Columbia‐Presbyterian Medical Center during 1991‐1994. Four of 161 patients (2.5%) had lymphoproliferative disease in the marrow; only 1 of these had a monoclonal paraprotein. Routine bone marrow examination of patients with MND increases the diagnostic yield of lymphoproliferative diseases. The frequency of these bone marrow abnormalities in comparison with a group of age‐matched control subjects should be studied further. © 1996 John Wiley & Sons, Inc. |
---|---|
Bibliography: | General Clinical Research Center - No. RR-00645 National Institute of Neurological Diseases & Stroke - No. NS 11766; No. NS 010863 istex:5B49C0B82B5A15E39DEE684BBEFA20718D59FF2B ark:/67375/WNG-SCM0V2QD-Z Eleanor and Cou Gehrig MDA/ALS Center Muscular Dystrophy Association ArticleID:MUS11 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0148-639X 1097-4598 |
DOI: | 10.1002/(SICI)1097-4598(199610)19:10<1334::AID-MUS11>3.0.CO;2-U |