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  Vol. 142 No. 3, March 1982 TABLE OF CONTENTS
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A Hypereosinophilic Syndrome With Retinal Arteritis and Tuberculosis

Jean P. Farcet, MD; Michel Binaghi, MD; Mathieu Kuentz, MD; Jean F. Merlier, MD; Claude Mayaud, MD; Thierry Nebout, MD; Patrick Nass, MD; Jacques Ferret, MD

Arch Intern Med. 1982;142(3):625-627.


Abstract

• A 35-year-old man was initially seen with a decrease in visual acuity, renal insufficiency, and elevation of the eosinophil count in the blood. The ocular syndrome was caused by extensive arterial occlusions of the retina. The subsequent apparition of cardiac, pulmonary, and neurologic signs fulfilled the criteria for the diagnosis of hypereosinophilic syndrome (HES). Most symptoms, including ocular, were temporarily but notably improved by hydroxyurea. The patient died after two years. An autopsy showed an endomyocardial fibrosis and disclosed destruction of the left kidney by an active tuberculosis. A pathogenic relationship between the infectious disease and the HES is envisaged.

(Arch Intern Med 1982;142:625-627)



Author Affiliations

From the Departments of Hematology (Drs Farcet, Kuentz, Nass, and Ferret), Ophthalmology (Dr Binaghi), and Nephrology (Dr Nebout), Hôpital Henri Mondor, Créteil, France; and the Department of Central Anatomy and Pathology (Dr Merlier) and Center for Pneumology (Dr Mayaud), Hôpital Tenon, Paris.


Footnotes

Accepted for publication Aug 3, 1981.

Reprints not available.



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

The FIP1L1-PDGFR{alpha} fusion tyrosine kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia: implications for diagnosis, classification, and management
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Blood 2004;103:2879-2891.
ABSTRACT | FULL TEXT  





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