Essential thrombocytosis historical perspective: Difference between revisions
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}}</ref> Subsequently, essential thrombocytosis was classified as a myeloproliferative disorder along with chronic myelogenous leukemia ([[CML]]), [[polycythemia vera]] (PV), and chronic idiopathic [[myelofibrosis]] (CIMF). | }}</ref> Subsequently, essential thrombocytosis was classified as a myeloproliferative disorder along with [[chronic myelogenous leukemia]] ([[CML]]), [[polycythemia vera]] (PV), and chronic idiopathic [[myelofibrosis]] (CIMF). | ||
==References== | ==References== |
Revision as of 14:41, 16 November 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Soujanya Thummathati, MBBS [2]
Overview
Essential thrombocytosis was first defined by Emil Epstein and Alfred Goedel, two Austrian pathologists, in the year 1934 and was initially called hemorrhagic thrombocythemia.[1]
Historical perspective
Essential thrombocytosis was first defined by Emil Epstein and Alfred Goedel, two Austrian pathologists, in the year 1934 and was initially called hemorrhagic thrombocythemia.[1] Subsequently, essential thrombocytosis was classified as a myeloproliferative disorder along with chronic myelogenous leukemia (CML), polycythemia vera (PV), and chronic idiopathic myelofibrosis (CIMF).
References
- ↑ 1.0 1.1 Steven Sanchez & April Ewton (2006). "Essential thrombocythemia: a review of diagnostic and pathologic features". Archives of pathology & laboratory medicine. 130 (8): 1144–1150. PMID 16879015. Unknown parameter
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