Thrombocytopenia differential diagnosis: Difference between revisions
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==Differential Diagnosis== | ==Differential Diagnosis== | ||
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!Category | |||
!Disease | |||
!History and symptoms | |||
!Laboratory findings | |||
!Pathology | |||
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| rowspan="2" |Cardiovascular | |||
|[[endocarditis]] | |||
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|[[pulmonary embolism]] | |||
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| rowspan="2" |Chemical/poisoning | |||
|[[Strontium-89]] | |||
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|[[zinc]] | |||
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| rowspan="4" |Dermatologic | |||
|[[Cholesterol embolism]] | |||
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|[[Elejalde syndrome]] | |||
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|[[Griscelli syndrome|Griscelli syndrome type 1]] | |||
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|[[neuroectodermal melanolysosomal disease]] | |||
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| rowspan="33" |Hematologic | |||
|[[Acquired pure megakaryocytic aplasia]] | |||
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|[[aplastic anemia]] | |||
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|[[Bernard-Soulier syndrome]] | |||
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|[[Thrombocytopenia|congenital amegakaryocytic thrombocytopenia (CAMT)]] | |||
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|[[disseminated intravascular coagulation]] | |||
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|[[Epstein's syndrome]] | |||
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|[[familial histiocytic reticulosis]] | |||
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|[[Gasser syndrome]] | |||
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|[[GATA1|GATA1-related cytopenia]] | |||
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|[[Glanzmann's thrombasthenia]] | |||
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|[[grey platelet syndrome]] | |||
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|[[hemolytic uremic syndrome]] | |||
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|[[histiocytosis X]] | |||
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|[[hypersplenism]] | |||
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|[[idiopathic thrombocytopenic purpura]] | |||
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|[[Jacobsen syndrome]] | |||
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|[[Kasabach-Merritt syndrome]] | |||
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|[[May-Hegglin anomaly]] | |||
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|[[Moschcowitz syndrome]] | |||
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|[[myelodysplastic syndrome]] | |||
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|[[myelofibrosis]] | |||
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|[[neonatal alloimmune thrombocytopenia]] | |||
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|[[pancytopenia]] | |||
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|Paris-Trousseau thrombocytopenia | |||
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|[[paroxysmal nocturnal hemoglobinuria]] | |||
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|[[post-transfusion purpura]] | |||
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|[[TAR syndrome|radial aplasia-thrombocytopenia syndrome]] | |||
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|[[Sebastian platelet syndrome]] | |||
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|[[Shwachman-Diamond syndrome]] | |||
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|[[thrombotic thrombocytopenic purpura]] | |||
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|[[Von Willebrand disease]] | |||
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|[[Werlhof disease]] | |||
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|[[Wiskott-Aldrich syndrome]] | |||
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==References== | ==References== |
Revision as of 14:12, 7 July 2018
Thrombocytopenia Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Thrombocytopenia differential diagnosis On the Web |
American Roentgen Ray Society Images of Thrombocytopenia differential diagnosis |
Risk calculators and risk factors for Thrombocytopenia differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Farbod Zahedi Tajrishi, M.D.
Overview
Thrombocytopenia has a broad range of potential causes. While a good history and physical examination can be helpful to diagnose some of these causes such as drug-induced thrombocytopenia, they usually don't suffice and further evaluation is often needed. There are also some useful points that may guide the physician to an appropriate diagnosis. For example, asymptomatic, isolated thrombocytopenia most probably suggests ITP, while thrombocytopenia in critically ill, hospitalized patients is usually suggestive of iatrogenic causes (eg. dilution), platelet consumption, bone marrow suppression from infection/sepsis, or even drug-induced thrombocytopenia. One should consider however, that a wide variety of other conditions such as autoimmune disorders, nutrient deficiencies, thrombotic microangiopathies could all as well cause thrombocytopenia.