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A Case of Hypereosinophilic Syndrome
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HOME > J Pathol Transl Med > Volume 16(3); 1982 > Article
Etc A Case of Hypereosinophilic Syndrome
Journal of Pathology and Translational Medicine 1982;16(3):567-573
DOI: https://doi.org/
Department of Clinical Pathology, School of Medicine, Han Yang University, Seoul, Korea
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Marked eosinophila is a common findings in many diseases, occuring most frequently in allergic and parasitic conditions. A separate syndrome has emerged over the past sixty years characterized by persistent marked eosinophilia of the blood associated with diffuse organ infiltration by eosinophiles. A variety of diagnoses have teen offered in these cases including eosinophilic leukemia, disseminated eosinophilic leukemia, disseminated eosinophilic collagen disease and Loeffler's fibroplastic endocarditis with eosinophilia even though clinical course, physical examination, laboratory data and autopsy finding often have teen similar, regardless of diagnosis. Therefore, recent workers have referred to these conditions as the hypereosinophilic syndrome. Fourth-two year old house-wife was visited to Han Yang Univ. Hospital on Mar. 31, 1981 due to epigastric pain and facial melasma. Laboratory data show a WBC of 13,700/cumm with 79% of eosinophils and 7,100/cumm of total eosinophilic count. Known cause of eosinophilia wart not found. And also, skin and liver biopsy findings reveal diffuse eosinophilic infiltration throughout the organ. So, authers report a case of Hypereosinophilic syndrome with brief review of literature.

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