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Eosinophilia-Myalgia SyndromeA Clinical Case Series of 21 Patients
Rossanne M. Philen, MD, MS;
Millicent Eidson, MA, DVM;
Edwin M. Kilbourne;
C. Mack Sewell, DrPH, MS;
Ron Voorhees, MD, MPH
Arch Intern Med. 1991;151(3):533-537.
Abstract
We reviewed 21 cases of eosinophilia-myalgia syndrome to describe the range of clinical findings in these patients. Most patients were women (20 [95%]) and middle-aged (mean, 46 years) and had taken the food supplement L-tryptophan (95%). All cases involved eosinophilia (eosinophil count, 2.0 x 109/L) and incapacitating myalgias. Fourteen (88%) of the 16 patients tested had mild liver function abnormalities. Aldolase levels were abnormal in all patients tested. Muscle biopsies were done in five patients; four showed eosinophilic perimyositis, and one had interstitial inflammation. No physical finding was pathognomonic or universal, but muscle tenderness, tachycardia, and rash were the most common signs found during physical examinations. Seven patients were treated with prednisone, and six showed improvement in muscle pain and a decrease in eosinophilia. The cause of this disorder is still unknown.
(Arch Intern Med. 1991;151:533-537)
Author Affiliations
New Mexico Eosinophilia-Myalgia Syndrome Study Group
From the Center for Environmental Health and Injury Control, Centers for Disease Control, Atlanta, Ga (Drs Philen and Kilbourne); and the Office of Epidemiology, New Mexico Health and Environment Department, Santa Fe (Drs Eidson, Sewell, and Voorhees).
Footnotes
Accepted for publication September 26, 1990.
Use of trade names is for identification only and does not constitute endorsement by the Public Health Service or the US Department of Health and Human Services.
Reprint requests to Center for Environmental Health and Injury Control, Mailstop F-28, Centers for Disease Control, 1600 Clifton Rd NE, Atlanta, GA 30333 (Dr Philen).
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