Thrombocytopenia differential diagnosis: Difference between revisions
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!Pathology | !Pathology | ||
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| rowspan="2" |Cardiovascular | | rowspan="2" |'''Cardiovascular''' | ||
|[[endocarditis]] | |[[endocarditis]] | ||
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| rowspan="2" |Chemical/poisoning | | rowspan="2" |'''Chemical/poisoning''' | ||
|[[Strontium-89]] | |[[Strontium-89]] | ||
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| rowspan="4" |Dermatologic | | rowspan="4" |'''Dermatologic''' | ||
|[[Cholesterol embolism]] | |[[Cholesterol embolism]] | ||
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| rowspan="33" |Hematologic | | rowspan="4" |'''Ear Nose Throat''' | ||
|[[Alport syndrome]] | |||
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|Arias oculootoradial syndrome | |||
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|[[Epstein's syndrome]] | |||
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|[[Fechtner syndrome]] | |||
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|'''Endocrine''' | |||
|[[Immunodysregulation polyendocrinopathy and enteropathy, X-linked]] | |||
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| rowspan="4" |'''Gastroenterologic''' | |||
|[[Aminoaciduria|Dibasic aminoaciduria type 2]] | |||
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|[[liver failure]] | |||
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|[[Niemann-Pick disease|Niemann-Pick disease type b]] | |||
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|[[portal hypertension]] | |||
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| rowspan="14" |'''Genetic''' | |||
|[[Aicardi-Goutieres syndrome]] | |||
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|[[Chediak-Higashi disease]] | |||
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|[[Factor H|complement factor H deficiency]] | |||
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|[[Elejalde syndrome]] | |||
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|[[Fanconi anaemia]] | |||
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|[[Fechtner syndrome]] | |||
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|[[Griscelli syndrome|Griscelli syndrome type 1]] | |||
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|[[holocarboxylase synthase deficiency]] | |||
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|[[iminodipeptiduria]] | |||
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|[[Jacobsen syndrome]] | |||
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|[[MELAS]] | |||
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|[[Omenn syndrome]] | |||
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|[[TAR syndrome]] | |||
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|[[X-linked hyperimmunoglobulin M syndrome]] | |||
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| rowspan="33" |'''Hematologic''' | |||
|[[Acquired pure megakaryocytic aplasia]] | |[[Acquired pure megakaryocytic aplasia]] | ||
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|[[Von Willebrand disease]] | |[[Von Willebrand disease|Von Willebrand disease, platelet type]] | ||
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| rowspan="5" |'''Iatrogenic''' | |||
|[[Coronary artery bypass surgery|Cardiac bypass]] | |||
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|[[chemotherapy]] | |||
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|[[Intra-aortic balloon pump|intra-aortic balloon pump placement]] | |||
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|[[Blood transfusion|massive blood transfusion]] | |||
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|[[radiation therapy]] | |||
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| rowspan="25" |'''Infectious diseases''' | |||
|[[Congenital syphilis]] | |||
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|[[cytomegalovirus]] | |||
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|[[Dengue fever]] | |||
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|[[ehrlichiosis]] | |||
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|[[Epstein-Barr virus]] | |||
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|[[hantavirus]] | |||
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|[[hepatitis C]] | |||
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|[[HIV]] | |||
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|[[human granulocytic ehrlichiosis]] | |||
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|[[Ehrlichiosis|human monocytotropic ehrlichiosis]] | |||
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|[[lassa fever]] | |||
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|[[leptospirosis]] | |||
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|[[malaria]] | |||
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|[[measles]] | |||
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|[[mumps]] | |||
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|[[mycoplasma pneumonia]] | |||
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|[[Relapsing fever|Oklahoma tick fever]] | |||
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|[[parvovirus]] | |||
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|[[Q fever]] | |||
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|[[rubella]] | |||
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|sepsis | |||
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|[[tick-borne encephalitis]] | |||
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|[[Toxic shock syndrome|toxic shock syndrome (staphylococcal)]] | |||
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|[[varicella]] | |||
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|[[visceral leishmaniasis]] | |||
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|'''Musculoskeletal/Orthopedic''' | |||
|[[cholesterol embolism]], [[TAR syndrome|radial aplasia-thrombocytopenia syndrome]], [[TAR syndrome]], [[TAR syndrome|thrombocytopenia absent radius syndrome]] | |||
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|'''Nutritional/Metabolic''' | |||
|[[Aminoaciduria|Dibasic aminoaciduria type 2]], [[folate deficiency]], [[Gaucher disease]], [[holocarboxylase synthase deficiency]], [[iminodipeptiduria]], [[iron deficiency]], [[isovaleric acidaemia]], [[Methylmalonic aciduria|methylmalonic aciduria type 2]], [[CD36|platelet glycoprotein 4 deficiency]], [[platelet glycoprotein Ib deficiency]], [[prolidase deficiency]], [[propionyl-CoA carboxylase deficiency]], [[sea blue histiocytosis]], [[sitosterolemia]], [[vitamin B12 deficiency]] | |||
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|'''Obstetric/Gynecologic''' | |||
|[[Eclampsia]], [[HELLP syndrome]], [[pre-eclampsia]] | |||
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|'''Oncologic''' | |||
|[[Acute lymphoblastic leukemia]], [[acute myeloid leukemia]], [[acute promyelocytic leukemia]], [[chronic lymphocytic leukaemia]], [[chronic myeloid leukaemia]], [[hairy cell leukaemia]], [[hepatosplenic T-cell lymphoma]], , [[lymphoma]], [[myeloma]], [[Non-Hodgkins lymphoma]], [[paraneoplastic syndrome]] | |||
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|'''Overdose/Toxicity''' | |||
|[[Alcohol]], [[arsenic trioxide]], [[ethanol]] | |||
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|'''Pulmonary''' | |||
|[[Acute respiratory distress syndrome]] | |||
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|'''Renal/Electrolyte''' | |||
|[[Epstein's syndrome]], [[Fechtner syndrome]], [[hemolytic uremic syndrome]] | |||
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|'''Rheumatology/Immunology/Allergy''' | |||
|[[Anticardiolipin syndrome]], [[antiphospholipid syndrome]], [[autoimmune lymphoproliferative syndrome type 1]], [[autoimmune lymphoproliferative syndrome type 2]], [[Factor H|complement factor H deficiency]], [[Evans syndrome]], [[immunodysregulation polyendocrinopathy and enteropathy, X-linked]], [[macrophage-activation syndrome]], [[neonatal alloimmune thrombocytopenia]], [[Omenn syndrome]], [[paraneoplastic syndrome]], [[systemic lupus erythematosus]], [[Wiskott-Aldrich syndrome]], [[X-linked hyperimmunoglobulin M syndrome]] | |||
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|'''Miscellaneous''' | |||
|[[Snakebites]] | |||
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Revision as of 14:42, 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.