Thrombocytopenia differential diagnosis: Difference between revisions
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|''' | | rowspan="14" |'''Nutritional/Metabolic''' | ||
|[[ | |[[folate deficiency]] | ||
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|[[Gaucher disease]] | |||
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|[[holocarboxylase synthase deficiency]] | |||
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|[[iminodipeptiduria]] | |||
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|''' | |[[iron deficiency]] | ||
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|[[isovaleric acidaemia]] | |||
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|[[Methylmalonic aciduria|methylmalonic aciduria type 2]] | |||
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|[[CD36|platelet glycoprotein 4 deficiency]] | |||
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|[[platelet glycoprotein Ib deficiency]] | |||
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|[[prolidase deficiency]] | |||
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|[[propionyl-CoA carboxylase deficiency]] | |||
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|[[sea blue histiocytosis]] | |||
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|[[sitosterolemia]] | |||
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|[[vitamin B12 deficiency]] | |||
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| rowspan="2" |'''Obstetric/Gynecologic''' | |||
|[[Eclampsia]], [[pre-eclampsia]] | |||
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|[[HELLP syndrome]] | |||
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| rowspan="11" |'''Oncologic''' | |||
|[[Acute lymphoblastic leukemia]] | |||
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|[[acute myeloid leukemia]] | |||
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|[[acute promyelocytic leukemia]] | |||
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|[[chronic lymphocytic leukaemia]] | |||
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|[[chronic myeloid leukaemia]] | |||
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|[[hairy cell leukaemia]] | |||
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|[[hepatosplenic T-cell lymphoma]] | |||
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|[[lymphoma]] | |||
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|[[myeloma]] | |||
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|[[Non-Hodgkins lymphoma]] | |||
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|[[paraneoplastic syndrome]] | |||
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| rowspan="2" |'''Overdose/Toxicity''' | |||
|[[ethanol]] | |||
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|[[arsenic trioxide]] | |||
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|'''Renal/Electrolyte''' | |'''Renal/Electrolyte''' | ||
| | |[[hemolytic uremic syndrome]] | ||
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|'''Rheumatology/Immunology/Allergy''' | | rowspan="10" |'''Rheumatology/Immunology/Allergy''' | ||
|[[Anticardiolipin | |[[Anticardiolipin syndrome]] | ||
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|[[antiphospholipid syndrome]] | |||
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|[[autoimmune lymphoproliferative syndrome type 1]] | |||
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|[[autoimmune lymphoproliferative syndrome type 2]] | |||
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|[[Factor H|complement factor H deficiency]] | |||
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|[[Evans syndrome]] | |||
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|[[immunodysregulation polyendocrinopathy and enteropathy, X-linked]] | |||
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|[[macrophage-activation syndrome]] | |||
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|[[neonatal alloimmune thrombocytopenia]] | |||
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|[[systemic lupus erythematosus]] | |||
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| | |'''Miscellaneous''' | ||
| | |[[Snakebites]] | ||
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Revision as of 17:27, 7 July 2018
Thrombocytopenia Microchapters |
Diagnosis |
---|
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.