Hypereosinophilic Multiple Thrombosis
- 1 June 1977
- journal article
- case report
- Published by SAGE Publications in Angiology
- Vol. 28 (6) , 361-375
- https://doi.org/10.1177/000331977702800601
Abstract
A case of marked chronic mature eosinophilia associated with multiple thrombosis in 30-year-old male is presented. Hitherto this sort of the disease has been categorized as DECD. Reviewing the autopsied cases of DECD, including our own case, DECD should not be categorized as a collagen disease because of the absent connective tissue degeneration and absent connective tissue degeneration and absent serological abnormalities. We rather noticed a certain relation between marked chronic mature eosinophilia and thrombus formation. Therefore, we propose here the term hypereosinophilic multiple thrombosis to express the pathomorphogenesis more precisely.Keywords
This publication has 18 references indexed in Scilit:
- Disseminated eosinophilic collagen diseaseThe American Journal of Medicine, 1974
- Pseudoeosinophilia, eosinophilic endocarditis and eosinophilic leukemiaThe American Journal of Medicine, 1972
- Eosinophilic Leukemia with Fibrosing Endocarditis and Short Y ChromosomeAnnals of Internal Medicine, 1972
- The Hypereosinophilic SyndromesAnnals of Internal Medicine, 1968
- Philadelphia chromosome in eosinophilic leukemiaThe American Journal of Medicine, 1965
- Eosinophilic Leukemia and Disseminated Eosinophilic Collagen Disease - a Disease Entity?Acta Medica Scandinavica, 1965
- EOSINOPHILIC LEUKÆMIA WITH Ph1-POSITIVE CELLSThe Lancet, 1964
- Fibroplastic parietal endocarditis with eosinophiliaThe American Journal of Medicine, 1963
- Eosinophilic leukemiaThe American Journal of Medicine, 1961
- Disseminated Eosinophilic “Collagen Disease”Acta Medica Scandinavica, 1955