Essential thrombocytosis history and symptoms: Difference between revisions
No edit summary |
No edit summary |
||
Line 3: | Line 3: | ||
==Overview== | ==Overview== | ||
People with Essential thrombocytosis are usually asymptomatic. Symptoms of ET may arise from vascular occlusion by thrombi or bleeding and may include vision disturbances, chest pain, intense burning pain in hands or feet([[erythromelalgia]]), numbness and tingling of hands and feet, [[priapism]] (persistent and painful erection of the penis). Neurologic symptoms like headache may occur but the pathophysiology is not completely understood. Rarely a family history may be present in patients with familial essential thrombocytosis. | |||
==History and symptoms== | ==History and symptoms== | ||
*People with Essential thrombocytosis are usually asymptomatic. Patients may have symptoms of minimal bleeding that go unnoticed until diagnosis. Most of the symptoms are vascular, either from thrombi occluding small and large blood vessels, though any blood vessel may be involved. Symptoms depend on the blood vessel involved. | |||
* | *Symptoms of vascular occlusion: | ||
*Vision disturbances | **[[Dizziness]] | ||
*Chest pain | **Vision disturbances | ||
*Intense burning pain in hands or feet(erythromelalgia) | **Chest pain | ||
*Numbness and tingling of hands and feet | **Intense burning pain in hands or feet(erythromelalgia) | ||
*Priapism | **Numbness and tingling of hands and feet | ||
**[[Priapism]] (persistent and painful erection of the penis) | |||
*Symptoms from bleeding can occur despite the increased platelet count accounting to the dysfunctional platelets. Common sites of bleeding include eyes, nose([[epistaxis]]), gums, gastrointestinal tract, skin(bruises). The bleeding itself is usually minimal. | |||
*Neurologic symptoms like headache may occur but the pathophysiology is not completely understood.<ref name="pmid17210076">{{cite journal| author=Brière JB| title=Essential thrombocythemia. | journal=Orphanet J Rare Dis | year= 2007 | volume= 2 | issue= | pages= 3 | pmid=17210076 | doi=10.1186/1750-1172-2-3 | pmc=PMC1781427 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17210076 }} </ref> | |||
==References== | ==References== |
Revision as of 19:32, 6 November 2015
Essential thrombocytosis Microchapters |
Differentiating Essential thrombocytosis from other Diseases |
---|
Diagnosis |
Treatment |
Essential thrombocytosis history and symptoms On the Web |
American Roentgen Ray Society Images of Essential thrombocytosis history and symptoms |
Risk calculators and risk factors for Essential thrombocytosis history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
People with Essential thrombocytosis are usually asymptomatic. Symptoms of ET may arise from vascular occlusion by thrombi or bleeding and may include vision disturbances, chest pain, intense burning pain in hands or feet(erythromelalgia), numbness and tingling of hands and feet, priapism (persistent and painful erection of the penis). Neurologic symptoms like headache may occur but the pathophysiology is not completely understood. Rarely a family history may be present in patients with familial essential thrombocytosis.
History and symptoms
- People with Essential thrombocytosis are usually asymptomatic. Patients may have symptoms of minimal bleeding that go unnoticed until diagnosis. Most of the symptoms are vascular, either from thrombi occluding small and large blood vessels, though any blood vessel may be involved. Symptoms depend on the blood vessel involved.
- Symptoms of vascular occlusion:
- Symptoms from bleeding can occur despite the increased platelet count accounting to the dysfunctional platelets. Common sites of bleeding include eyes, nose(epistaxis), gums, gastrointestinal tract, skin(bruises). The bleeding itself is usually minimal.
- Neurologic symptoms like headache may occur but the pathophysiology is not completely understood.[1]
References
- ↑ Brière JB (2007). "Essential thrombocythemia". Orphanet J Rare Dis. 2: 3. doi:10.1186/1750-1172-2-3. PMC 1781427. PMID 17210076.