Polycythemia: Difference between revisions
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{{SK}} Polycythaemia, erythrocythemia, erythrocytosis, packed cell volume increased, PCV increased, primary familial and congenital polycythemia, PFCP, familial erythrocytosis, hereditary erythrocytosis, congenital erythrocytosis, inherited erythrocytosis | {{SK}} Polycythaemia, erythrocythemia, erythrocytosis, packed cell volume increased, PCV increased, primary familial and congenital polycythemia, PFCP, familial erythrocytosis, hereditary erythrocytosis, congenital erythrocytosis, inherited erythrocytosis | ||
==[[Polycythemia overview|Overview]]== | ==[[Polycythemia overview|Overview]]== Polycythemia falls under the category of conditions called myeloproliferative neoplasms with an underlying mutation especially JAK2V617F. These disorders are characterised by an abnormal proliferation of both immature and mature myeloid cells. | ||
{{cite journal |vauthors=Parnes A, Ravi A |title=Polycythemia and Thrombocytosis |journal=Prim Care |volume=43 |issue=4 |pages=589–605 |date=December 2016 |pmid=27866579 |doi=10.1016/j.pop.2016.07.011 |url=}} | |||
==[[Polycythemia historical perspective|Historical Perspective]]== | ==[[Polycythemia historical perspective|Historical Perspective]]== | ||
Revision as of 00:41, 5 November 2020
For patient information on Neonatal polycythemia, click here
For patient information on Polycythemia vera, click here
| Polycythemia | |
| ICD-10 | D45, D75.1 |
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| ICD-9 | 238.4, 289.0, 776.4 |
| DiseasesDB | 10295 |
| MeSH | D011086 |
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Polycythemia Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Polycythemia On the Web |
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American Roentgen Ray Society Images of Polycythemia |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Debduti Mukhopadhyay, M.B.B.S[2]
Synonyms and keywords: Polycythaemia, erythrocythemia, erythrocytosis, packed cell volume increased, PCV increased, primary familial and congenital polycythemia, PFCP, familial erythrocytosis, hereditary erythrocytosis, congenital erythrocytosis, inherited erythrocytosis
==Overview== Polycythemia falls under the category of conditions called myeloproliferative neoplasms with an underlying mutation especially JAK2V617F. These disorders are characterised by an abnormal proliferation of both immature and mature myeloid cells. Parnes A, Ravi A (December 2016). "Polycythemia and Thrombocytosis". Prim Care. 43 (4): 589–605. doi:10.1016/j.pop.2016.07.011. PMID 27866579.
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Polycythemia from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Diagnostic study of choice | History and Symptoms | Physical Examination | Laboratory Findings | X-Ray Findings | Echocardiography or Ultrasound | CT-Scan Findings | MRI Findings | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Interventions | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies
Case Studies
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