Polycythemia vera differential diagnosis: Difference between revisions
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||[[Polycythemia vera (PV)]] | ||[[Polycythemia vera (PV)]] | ||
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* JAK2 mutation (V617F or exon 12 mutation) | * JAK2 mutation (V617F or exon 12 mutation) in more than 95% of cases | ||
* Autonomous erythrocyte production | * Autonomous erythrocyte production | ||
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* Clonal proliferation of megakaryocytes | * Clonal proliferation of megakaryocytes | ||
* Excess [[platelet]] production | * Excess [[platelet]] production | ||
* | * Caused by JAK2 mutation in 50% of cases | ||
* Caused by CALR mutation in some cases | |||
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* Stroke-like symptoms | * Stroke-like symptoms |
Revision as of 23:28, 28 January 2018
Polycythemia vera Microchapters |
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Treatment |
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Polycythemia vera differential diagnosis On the Web |
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Risk calculators and risk factors for Polycythemia vera differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Mohamad Alkateb, MBBCh [2] Shyam Patel [3]
Overview
Polycythemia vera must be differentiated from chronic myelogenous leukemia, essential thrombocythemia, and primary myelofibrosis.[1][2]
Differential Diagnosis
Polycythemia vera must be differentiated from a variety of other conditions.
Characteristic/Parameter | Etiology | Symptoms | Laboratory abnormalities | Physical examination | Treatment | Other associated abnormalities |
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Polycythemia vera (PV) |
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Essential thrombocythemia (ET) |
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Chronic myeloid leukemia (CML) |
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Primary myelofibrosis (PMF) |
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References
- ↑ 1.0 1.1 Tefferi A, Barbui T (2015). "Polycythemia vera and essential thrombocythemia: 2015 update on diagnosis, risk-stratification and management". Am J Hematol. 90 (2): 162–73. doi:10.1002/ajh.23895. PMID 25611051.
- ↑ 2.0 2.1 Sanchez S, Ewton A (2006). "Essential thrombocythemia: a review of diagnostic and pathologic features". Arch Pathol Lab Med. 130 (8): 1144–50. doi:10.1043/1543-2165(2006)130[1144:ET]2.0.CO;2. PMID 16879015.
- ↑ Jabbour E, Kantarjian H (2014). "Chronic myeloid leukemia: 2014 update on diagnosis, monitoring, and management". Am J Hematol. 89 (5): 547–56. doi:10.1002/ajh.23691. PMID 24729196.