Thrombocytosis differential diagnosis: Difference between revisions
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==Thrombocytosis Differential Diagnosis== | ==Thrombocytosis Differential Diagnosis== | ||
'''Differentiating the diseases that can cause | '''Differentiating the diseases that can cause thrombocytosis :''' | ||
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! rowspan="4" style="background: #4479BA; color: #FFFFFF; text-align: center;" |'''Reactive thrombocytosis''' | ! rowspan="4" style="background: #4479BA; color: #FFFFFF; text-align: center;" |'''Reactive thrombocytosis''' | ||
! align="center" style="background:#DCDCDC;" + |Anemia/ | ! align="center" style="background:#DCDCDC;" + |Anemia/ | ||
blood loss | |||
|Iron deficiency, blood loss, hemolysis | |Iron deficiency, blood loss, hemolysis | ||
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!Infection | !Infection |
Revision as of 19:44, 22 August 2018
Thrombocytosis Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Thrombocytosis differential diagnosis On the Web |
American Roentgen Ray Society Images of Thrombocytosis differential diagnosis |
Risk calculators and risk factors for Thrombocytosis differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2]
Overview
Thrombocytosis Differential Diagnosis
Differentiating the diseases that can cause thrombocytosis :
Category | Condition | Etiology | Mechanism | Inherited | Acquried | Clinical manifestations | Para−clinical findings | Gold standard | Associated findings | |||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Demography | History | Symptoms | Signs | |||||||||||||||||||||||||
Lab Findings | Imaging | |||||||||||||||||||||||||||
Fever | Rash | Bleeding | BP | Splenomegaly | Jaundice | Other | CBC | PBS | Bone marrow exam | PT | PTT | UA | ||||||||||||||||
Decreased platelet production | Platelet destruction in blood | Platelet destruction in spleen | Plt | HB | WBC | |||||||||||||||||||||||
Autonomous thrombocytosis | Hematologic malignancies | Essential thrombocythemia | ||||||||||||||||||||||||||
Polycythemia vera | ||||||||||||||||||||||||||||
Primary myelofibrosis | ||||||||||||||||||||||||||||
Chronic myeloid leukemia | ||||||||||||||||||||||||||||
Myelodysplastic syndromes[1] |
|
+ | - | - | -/+ | + | Elderly | Exposure to | + | Petechiae, purpura, diffuse erythematous rash | + | Nl | + | + | Shortness of breath, fatigue | ↓ | ↓ | ↓ |
|
|
Nl | Nl | Nl | NA | Bone marrow examination + clinical manifestation |
| ||
Acute myeloid leukemia | + | |||||||||||||||||||||||||||
Familial thrombocytosis | ||||||||||||||||||||||||||||
Category | Condition | Etiology | Decreased platelet production | Platelet destruction in blood | Platelet destruction in spleen | Inherited | Acquried | Demography | History | Fever | Rash | Bleeding | BP | Splenomegaly | Jaundice | Other signs | Plt | HB | WBC | PBS | Bone marrow exam | PT | PTT | UA | Imaging | Gold standard | Associated findings | |
Reactive thrombocytosis | Anemia/
blood loss |
Iron deficiency, blood loss, hemolysis | ||||||||||||||||||||||||||
Infection | Viral, bacterial, mycobacterial, and fungal causes | |||||||||||||||||||||||||||
Non-infectious inflammation | Malignancy, rheumatologic conditions, trauma, reactions to medications | |||||||||||||||||||||||||||
Post-splenectomy | Post-splenectomy or functional asplenia (eg, sickle cell disease) | |||||||||||||||||||||||||||
Category | Condition | Etiology | Decreased platelet production | Platelet destruction in blood | Platelet destruction in spleen | Inherited | Acquried | Demography | History | Fever | Rash | Bleeding | BP | Splenomegaly | Jaundice | Other signs | Plt | HB | WBC | PBS | Bone marrow exam | PT | PTT | UA | Imaging | Gold standard | Associated findings |
References
- ↑ Natelson, Ethan A.; Pyatt, David (2013). "Acquired Myelodysplasia or Myelodysplastic Syndrome: Clearing the Fog". Advances in Hematology. 2013: 1–11. doi:10.1155/2013/309637. ISSN 1687-9104.