Thrombocytopenia differential diagnosis: Difference between revisions
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! colspan="3" |Laboratory findings | ! colspan="3" |Laboratory findings | ||
! rowspan="2" |Pathology | ! rowspan="2" |Pathology | ||
! rowspan="2" |Other specifics | |||
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|[[White blood cells|WBC]] changes | |[[White blood cells|WBC]] changes | ||
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* ↑ [[Erythrocyte sedimentation rate|ESR]] | * ↑ [[Erythrocyte sedimentation rate|ESR]] | ||
* ↑ [[Rheumatoid factor|RF]], [[Blood urea nitrogen|BUN]] and [[Creatinine|Cr]] may also be present | * ↑ [[Rheumatoid factor|RF]], [[Blood urea nitrogen|BUN]] and [[Creatinine|Cr]] may also be present | ||
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|[[pulmonary embolism]] | |[[pulmonary embolism]]<ref name="pmid241826422">{{cite journal| author=Cohen AT, Dobromirski M, Gurwith MM| title=Managing pulmonary embolism from presentation to extended treatment. | journal=Thromb Res | year= 2014 | volume= 133 | issue= 2 | pages= 139-48 | pmid=24182642 | doi=10.1016/j.thromres.2013.09.040 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24182642 }}</ref> | ||
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* [[Dyspnea]] | |||
* [[Pleuritic chest pain]] | |||
* [[Fainting]] | |||
* [[Cough]] | |||
* [[Substernal chest pain]] | |||
* [[Hemoptysis]] | |||
* [[Wheezing]] | |||
* [[Cyanosis]] | |||
* [[Fever]] | |||
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| rowspan="2" |'''Chemical/poisoning''' | | rowspan="2" |'''Chemical/poisoning''' | ||
|[[Strontium-89]] | |[[Strontium-89]] | ||
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|[[zinc]] | |[[zinc]] | ||
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| rowspan="4" |'''Dermatologic''' | | rowspan="4" |'''Dermatologic''' | ||
|[[Cholesterol embolism]] | |[[Cholesterol embolism]] | ||
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|[[Elejalde syndrome]] | |[[Elejalde syndrome]] | ||
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|[[Griscelli syndrome|Griscelli syndrome type 1]] | |[[Griscelli syndrome|Griscelli syndrome type 1]] | ||
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|[[neuroectodermal melanolysosomal disease]] | |[[neuroectodermal melanolysosomal disease]] | ||
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| rowspan="4" |'''Ear Nose Throat''' | | rowspan="4" |'''Ear Nose Throat''' | ||
|[[Alport syndrome]] | |[[Alport syndrome]] | ||
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|Arias oculootoradial syndrome | |Arias oculootoradial syndrome | ||
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|[[Epstein's syndrome]] | |[[Epstein's syndrome]] | ||
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|[[Fechtner syndrome]] | |[[Fechtner syndrome]] | ||
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|'''Endocrine''' | |'''Endocrine''' | ||
|[[Immunodysregulation polyendocrinopathy and enteropathy, X-linked]] | |[[Immunodysregulation polyendocrinopathy and enteropathy, X-linked]] | ||
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| rowspan="4" |'''Gastroenterologic''' | | rowspan="4" |'''Gastroenterologic''' | ||
|[[Aminoaciduria|Dibasic aminoaciduria type 2]] | |[[Aminoaciduria|Dibasic aminoaciduria type 2]] | ||
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|[[liver failure]] | |[[liver failure]] | ||
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|[[Niemann-Pick disease|Niemann-Pick disease type b]] | |[[Niemann-Pick disease|Niemann-Pick disease type b]] | ||
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|[[portal hypertension]] | |[[portal hypertension]] | ||
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| rowspan="14" |'''Genetic''' | | rowspan="14" |'''Genetic''' | ||
|[[Aicardi-Goutieres syndrome]] | |[[Aicardi-Goutieres syndrome]] | ||
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|[[Chediak-Higashi disease]] | |[[Chediak-Higashi disease]] | ||
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|[[Factor H|complement factor H deficiency]] | |[[Factor H|complement factor H deficiency]] | ||
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|[[Elejalde syndrome]] | |[[Elejalde syndrome]] | ||
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|[[Fanconi anaemia]] | |[[Fanconi anaemia]] | ||
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|[[Fechtner syndrome]] | |[[Fechtner syndrome]] | ||
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|[[Griscelli syndrome|Griscelli syndrome type 1]] | |[[Griscelli syndrome|Griscelli syndrome type 1]] | ||
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|[[holocarboxylase synthase deficiency]] | |[[holocarboxylase synthase deficiency]] | ||
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|[[iminodipeptiduria]] | |[[iminodipeptiduria]] | ||
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|[[Jacobsen syndrome]] | |[[Jacobsen syndrome]] | ||
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|[[MELAS]] | |[[MELAS]] | ||
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|[[Omenn syndrome]] | |[[Omenn syndrome]] | ||
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|[[TAR syndrome]] | |[[TAR syndrome]] | ||
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|[[X-linked hyperimmunoglobulin M syndrome]] | |[[X-linked hyperimmunoglobulin M syndrome]] | ||
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| rowspan="33" |'''Hematologic''' | | rowspan="33" |'''Hematologic''' | ||
|[[Acquired pure megakaryocytic aplasia]] | |[[Acquired pure megakaryocytic aplasia]] | ||
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|<nowiki>+ / ↓</nowiki> | |<nowiki>+ / ↓</nowiki> | ||
|<nowiki>+ / ↓</nowiki> | |<nowiki>+ / ↓</nowiki> | ||
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|[[Bernard-Soulier syndrome]] | |[[Bernard-Soulier syndrome]] | ||
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|[[Thrombocytopenia|congenital amegakaryocytic thrombocytopenia (CAMT)]] | |[[Thrombocytopenia|congenital amegakaryocytic thrombocytopenia (CAMT)]] | ||
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|[[disseminated intravascular coagulation]] | |[[disseminated intravascular coagulation]] | ||
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|[[Epstein's syndrome]] | |[[Epstein's syndrome]] | ||
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|[[familial histiocytic reticulosis]] | |[[familial histiocytic reticulosis]] | ||
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|[[Gasser syndrome]] | |[[Gasser syndrome]] | ||
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|[[GATA1|GATA1-related cytopenia]] | |[[GATA1|GATA1-related cytopenia]] | ||
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|[[Glanzmann's thrombasthenia]] | |[[Glanzmann's thrombasthenia]] | ||
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|[[grey platelet syndrome]] | |[[grey platelet syndrome]] | ||
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|[[hemolytic uremic syndrome]] | |[[hemolytic uremic syndrome]] | ||
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|[[histiocytosis X]] | |[[histiocytosis X]] | ||
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|[[hypersplenism]] | |[[hypersplenism]] | ||
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|[[idiopathic thrombocytopenic purpura]] | |[[idiopathic thrombocytopenic purpura]] | ||
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|[[Jacobsen syndrome]] | |[[Jacobsen syndrome]] | ||
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|[[Kasabach-Merritt syndrome]] | |[[Kasabach-Merritt syndrome]] | ||
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|[[May-Hegglin anomaly]] | |[[May-Hegglin anomaly]] | ||
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|[[Moschcowitz syndrome]] | |[[Moschcowitz syndrome]] | ||
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|[[myelodysplastic syndrome]] | |[[myelodysplastic syndrome]] | ||
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|[[myelofibrosis]] | |[[myelofibrosis]] | ||
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|[[neonatal alloimmune thrombocytopenia]] | |[[neonatal alloimmune thrombocytopenia]] | ||
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|[[pancytopenia]] | |[[pancytopenia]] | ||
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|Paris-Trousseau thrombocytopenia | |Paris-Trousseau thrombocytopenia | ||
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|[[paroxysmal nocturnal hemoglobinuria]] | |[[paroxysmal nocturnal hemoglobinuria]] | ||
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|[[post-transfusion purpura]] | |[[post-transfusion purpura]] | ||
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|[[TAR syndrome|radial aplasia-thrombocytopenia syndrome]] | |[[TAR syndrome|radial aplasia-thrombocytopenia syndrome]] | ||
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|[[Sebastian platelet syndrome]] | |[[Sebastian platelet syndrome]] | ||
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|[[Shwachman-Diamond syndrome]] | |[[Shwachman-Diamond syndrome]] | ||
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|[[thrombotic thrombocytopenic purpura]] | |[[thrombotic thrombocytopenic purpura]] | ||
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|[[Von Willebrand disease|Von Willebrand disease, platelet type]] | |[[Von Willebrand disease|Von Willebrand disease, platelet type]] | ||
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|[[Werlhof disease]] | |[[Werlhof disease]] | ||
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|[[Wiskott-Aldrich syndrome]] | |[[Wiskott-Aldrich syndrome]] | ||
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| rowspan="5" |'''Iatrogenic''' | | rowspan="5" |'''Iatrogenic''' | ||
|[[Coronary artery bypass surgery|Cardiac bypass]] | |[[Coronary artery bypass surgery|Cardiac bypass]] | ||
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|[[chemotherapy]] | |[[chemotherapy]] | ||
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|[[Intra-aortic balloon pump|intra-aortic balloon pump placement]] | |[[Intra-aortic balloon pump|intra-aortic balloon pump placement]] | ||
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|[[Blood transfusion|massive blood transfusion]] | |[[Blood transfusion|massive blood transfusion]] | ||
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|[[radiation therapy]] | |[[radiation therapy]] | ||
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| rowspan="25" |'''Infectious diseases''' | | rowspan="25" |'''Infectious diseases''' | ||
|[[Congenital syphilis]] | |[[Congenital syphilis]] | ||
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|[[cytomegalovirus]] | |[[cytomegalovirus]] | ||
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|[[Dengue fever]] | |[[Dengue fever]] | ||
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|[[ehrlichiosis]] | |[[ehrlichiosis]] | ||
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|[[Epstein-Barr virus]] | |[[Epstein-Barr virus]] | ||
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|[[hantavirus]] | |[[hantavirus]] | ||
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|[[hepatitis C]] | |[[hepatitis C]] | ||
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|[[HIV]] | |[[HIV]] | ||
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|[[human granulocytic ehrlichiosis]] | |[[human granulocytic ehrlichiosis]] | ||
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|[[Ehrlichiosis|human monocytotropic ehrlichiosis]] | |[[Ehrlichiosis|human monocytotropic ehrlichiosis]] | ||
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|[[lassa fever]] | |[[lassa fever]] | ||
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|[[leptospirosis]] | |[[leptospirosis]] | ||
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|[[malaria]] | |[[malaria]] | ||
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Line 605: | Line 697: | ||
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|[[measles]] | |[[measles]] | ||
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|[[mumps]] | |[[mumps]] | ||
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|[[mycoplasma pneumonia]] | |[[mycoplasma pneumonia]] | ||
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|[[Relapsing fever|Oklahoma tick fever]] | |[[Relapsing fever|Oklahoma tick fever]] | ||
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|[[parvovirus]] | |[[parvovirus]] | ||
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|[[Q fever]] | |[[Q fever]] | ||
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|[[rubella]] | |[[rubella]] | ||
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|sepsis | |sepsis | ||
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|[[tick-borne encephalitis]] | |[[tick-borne encephalitis]] | ||
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|[[Toxic shock syndrome|toxic shock syndrome (staphylococcal)]] | |[[Toxic shock syndrome|toxic shock syndrome (staphylococcal)]] | ||
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|[[varicella]] | |[[varicella]] | ||
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Line 682: | Line 785: | ||
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|[[visceral leishmaniasis]] | |[[visceral leishmaniasis]] | ||
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| rowspan="14" |'''Nutritional/Metabolic''' | | rowspan="14" |'''Nutritional/Metabolic''' | ||
|[[folate deficiency]] | |[[folate deficiency]] | ||
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Line 697: | Line 802: | ||
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|[[Gaucher disease]] | |[[Gaucher disease]] | ||
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|[[holocarboxylase synthase deficiency]] | |[[holocarboxylase synthase deficiency]] | ||
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Line 711: | Line 818: | ||
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|[[iminodipeptiduria]] | |[[iminodipeptiduria]] | ||
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|[[iron deficiency]] | |[[iron deficiency]] | ||
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Line 725: | Line 834: | ||
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|[[isovaleric acidaemia]] | |[[isovaleric acidaemia]] | ||
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|[[Methylmalonic aciduria|methylmalonic aciduria type 2]] | |[[Methylmalonic aciduria|methylmalonic aciduria type 2]] | ||
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|[[CD36|platelet glycoprotein 4 deficiency]] | |[[CD36|platelet glycoprotein 4 deficiency]] | ||
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Line 746: | Line 858: | ||
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|[[platelet glycoprotein Ib deficiency]] | |[[platelet glycoprotein Ib deficiency]] | ||
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Line 753: | Line 866: | ||
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|[[prolidase deficiency]] | |[[prolidase deficiency]] | ||
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|[[propionyl-CoA carboxylase deficiency]] | |[[propionyl-CoA carboxylase deficiency]] | ||
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|[[sea blue histiocytosis]] | |[[sea blue histiocytosis]] | ||
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Line 774: | Line 890: | ||
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|[[sitosterolemia]] | |[[sitosterolemia]] | ||
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Line 781: | Line 898: | ||
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|[[vitamin B12 deficiency]] | |[[vitamin B12 deficiency]] | ||
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| rowspan="2" |'''Obstetric/Gynecologic''' | | rowspan="2" |'''Obstetric/Gynecologic''' | ||
|[[Eclampsia]], [[pre-eclampsia]] | |[[Eclampsia]], [[pre-eclampsia]] | ||
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Line 796: | Line 915: | ||
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|[[HELLP syndrome]] | |[[HELLP syndrome]] | ||
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| rowspan="11" |'''Oncologic''' | | rowspan="11" |'''Oncologic''' | ||
|[[Acute lymphoblastic leukemia]] | |[[Acute lymphoblastic leukemia]] | ||
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Line 811: | Line 932: | ||
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|[[acute myeloid leukemia]] | |[[acute myeloid leukemia]] | ||
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Line 818: | Line 940: | ||
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|[[acute promyelocytic leukemia]] | |[[acute promyelocytic leukemia]] | ||
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Line 825: | Line 948: | ||
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|[[chronic lymphocytic leukaemia]] | |[[chronic lymphocytic leukaemia]] | ||
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Line 832: | Line 956: | ||
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|[[chronic myeloid leukaemia]] | |[[chronic myeloid leukaemia]] | ||
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Line 839: | Line 964: | ||
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|[[hairy cell leukaemia]] | |[[hairy cell leukaemia]] | ||
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Line 846: | Line 972: | ||
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|[[hepatosplenic T-cell lymphoma]] | |[[hepatosplenic T-cell lymphoma]] | ||
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Line 853: | Line 980: | ||
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|[[lymphoma]] | |[[lymphoma]] | ||
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|[[Non-Hodgkins lymphoma]] | |[[Non-Hodgkins lymphoma]] | ||
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|[[paraneoplastic syndrome]] | |[[paraneoplastic syndrome]] | ||
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| rowspan="2" |'''Overdose/Toxicity''' | | rowspan="2" |'''Overdose/Toxicity''' | ||
|[[ethanol]] | |[[ethanol]] | ||
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|[[arsenic trioxide]] | |[[arsenic trioxide]] | ||
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|'''Pulmonary''' | |'''Pulmonary''' | ||
|[[Acute respiratory distress syndrome]] | |[[Acute respiratory distress syndrome]] | ||
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|'''Renal/Electrolyte''' | |'''Renal/Electrolyte''' | ||
|[[hemolytic uremic syndrome]] | |[[hemolytic uremic syndrome]] | ||
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| rowspan="10" |'''Rheumatology/Immunology/Allergy''' | | rowspan="10" |'''Rheumatology/Immunology/Allergy''' | ||
|[[Anticardiolipin syndrome]] | |[[Anticardiolipin syndrome]] | ||
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|[[antiphospholipid syndrome]] | |[[antiphospholipid syndrome]] | ||
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|[[autoimmune lymphoproliferative syndrome type 1]] | |[[autoimmune lymphoproliferative syndrome type 1]] | ||
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|[[Factor H|complement factor H deficiency]] | |[[Factor H|complement factor H deficiency]] | ||
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|[[Evans syndrome]] | |[[Evans syndrome]] | ||
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|[[immunodysregulation polyendocrinopathy and enteropathy, X-linked]] | |[[immunodysregulation polyendocrinopathy and enteropathy, X-linked]] | ||
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|[[macrophage-activation syndrome]] | |[[macrophage-activation syndrome]] | ||
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|[[neonatal alloimmune thrombocytopenia]] | |[[neonatal alloimmune thrombocytopenia]] | ||
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|[[systemic lupus erythematosus]] | |[[systemic lupus erythematosus]] | ||
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|'''Miscellaneous''' | |'''Miscellaneous''' | ||
|[[Snakebites]] | |[[Snakebites]] | ||
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Revision as of 10:18, 8 August 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.
Differential Diagnosis
References
- ↑ Cohen AT, Dobromirski M, Gurwith MM (2014). "Managing pulmonary embolism from presentation to extended treatment". Thromb Res. 133 (2): 139–48. doi:10.1016/j.thromres.2013.09.040. PMID 24182642.