Easy bruising: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
|||
(19 intermediate revisions by 3 users not shown) | |||
Line 1: | Line 1: | ||
{{CMG}} {{RT}} | {{CMG}}; {{AE}} {{RT}} | ||
==Overview== | |||
==Causes== | |||
== | ===Common Causes=== | ||
*[[Acute lymphoblastic leukemia]] | |||
*[[Acute myeloid leukemia]] | |||
*[[Aging]] | |||
*[[Aspirin]] | |||
*[[Chronic lymphocytic leukemia]] | |||
*[[Chronic myelogenous leukemia]] | |||
*[[Chronic renal insufficiency]] | |||
*[[Chronic viral hepatitis]] | |||
*[[Cirrhosis]] | |||
*[[Dengue Fever]] | |||
*[[Factor VII deficiency]] | |||
*[[Factor V deficiency]] | |||
*[[Hemophilia A]] | |||
*[[Hemophilia B]] | |||
*[[Liver disease]] | |||
*[[Malnutrition]] | |||
*[[NSAIDs]] | |||
*[[Sepsis]] | |||
*[[Steroid]] use | |||
*[[Thrombocytopenia]] | |||
*[[Von Willebrand's Disease]] | |||
===Causes by Organ System=== | |||
{|style="width:80%; height:100px" border="1" | {|style="width:80%; height:100px" border="1" | ||
Line 64: | Line 88: | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Hematologic''' | | '''Hematologic''' | ||
|bgcolor="Beige"| [[Anti-factor VIIIc syndrome]], [[ATRUS syndrome]], [[Acute leukaemia of ambiguous lineage]], [[Acquired amegakaryocytic thrombocytopenia]], [[Acquired hypoprothrombinemia]], [[Acquired pure megakaryocytic aplasia]], [[Acute biphenotypic leukemia]], [[Acute erythroleukemia]], [[Acute lymphoblastic leukemia]], [[Acute megacaryoblastic leukemia]], [[Acute myelocytic leukemia]], [[Acute myeloid leukemia]], [[Acute non lymphoblastic leukemia]], [[Acute promyelocytic leukemia]], [[Deficiency of ADP platelet receptor P2Y12]], [[Congenital Anti-plasmin deficiency]], [[Aplastic anemia]], [[Bernard-Soulier Syndrome]], [[Chronic Idiopathic Myelofibrosis]], [[Chronic lymphocytic leukemia]], [[Chronic myelogenous leukemia]], [[Chronic myeloid leukemia]], [[Chronic myelomonocytic leukemia]], [[Myeloproliferative Disorders]], [[Chronic Neutrophilic Leukemia]], [[Familial CML-Like Syndrome]], [[Congenital amegakaryocytic thrombocytopenia]], [[DIC]], [[Essential thrombocytopenia]], [[Essential thrombocytosis]], [[Factor IX Deficiency]], [[Combined deficiency of Factor V and factor VIII]], [[Factor V deficiency]], [[Factor VII deficiency]], [[Factor X deficiency]], [[Familial platelet syndrome with predisposition to acute myelogenous leukemia]], [[Glanzmann Thrombasthenia]], [[Hairy cell leukemia]], [[Familial Hemophagocytic lymphohistiocytosis]], [[Hemophilia A]], [[Hemophilia B]], [[Hereditary macrothrombocytopenia]], [[Immune thrombocytopenic purpura]], [[Idiopathic thrombocytopenic purpura]], [[ Chronic T-cell leukemia]], [[Lymphoblastic lymphoma]], [[Multiple myeloma]], [[Myelofibrosis]],[[Myelogenous leukemia]], [[Pancytopenia]], [[Paroxysmal Nocturnal Hemoglobinuria]], [[Prothrombin deficiency]], [[Storage pool platelet disease]], [[Stuart factor deficiency]], [[T-cell acute lymphoblastic leukemia]], [[Thrombasthenia]], [[Thrombocytopathy]], [[Thrombocytopenia -- cerebellar hypoplasia -- short stature]], [[ | |bgcolor="Beige"| [[Anti-factor VIIIc syndrome]], [[ATRUS syndrome]], [[Acute leukaemia of ambiguous lineage]], [[Acquired amegakaryocytic thrombocytopenia]], [[Acquired hypoprothrombinemia]], [[Acquired pure megakaryocytic aplasia]], [[Acute biphenotypic leukemia]], [[Acute erythroleukemia]], [[Acute lymphoblastic leukemia]], [[Acute megacaryoblastic leukemia]], [[Acute myelocytic leukemia]], [[Acute myeloid leukemia]], [[Acute non lymphoblastic leukemia]], [[Acute promyelocytic leukemia]], [[Deficiency of ADP platelet receptor P2Y12]], [[Congenital Anti-plasmin deficiency]], [[Aplastic anemia]], [[Bernard-Soulier Syndrome]], [[Chronic Idiopathic Myelofibrosis]], [[Chronic lymphocytic leukemia]], [[Chronic myelogenous leukemia]], [[Chronic myeloid leukemia]], [[Chronic myelomonocytic leukemia]], [[Myeloproliferative Disorders]], [[Chronic Neutrophilic Leukemia]], [[Familial CML-Like Syndrome]], [[Congenital amegakaryocytic thrombocytopenia]], [[DIC]], [[Essential thrombocytopenia]], [[Essential thrombocytosis]], [[Factor IX Deficiency]], [[Combined deficiency of Factor V and factor VIII]], [[Factor V deficiency]], [[Factor VII deficiency]], [[Factor X deficiency]], [[Familial platelet syndrome with predisposition to acute myelogenous leukemia]], [[Glanzmann Thrombasthenia]], [[Hairy cell leukemia]], [[Familial Hemophagocytic lymphohistiocytosis]], [[Hemophilia A]], [[Hemophilia B]], [[Hereditary macrothrombocytopenia]], [[Immune thrombocytopenic purpura]], [[Idiopathic thrombocytopenic purpura]], [[ Chronic T-cell leukemia]], [[Lymphoblastic lymphoma]], [[Multiple myeloma]], [[Myelofibrosis]],[[Myelogenous leukemia]], [[Pancytopenia]], [[Paroxysmal Nocturnal Hemoglobinuria]], [[Prothrombin deficiency]], [[Storage pool platelet disease]], [[Stuart factor deficiency]], [[T-cell acute lymphoblastic leukemia]], [[Thrombasthenia]], [[Thrombocytopathy]], [[Thrombocytopenia -- cerebellar hypoplasia -- short stature]], [[Thrombocytopenia]], [[Von Willebrand's Disease]], [[Waldenstrom macroglobulinemia]], [[Retinopathy -- aplastic anemia -- neurological abnormalities]], [[May-Hegglin Anomaly]], [[Owren Parahemophilia]], [[X-linked dyserythropoietic anaemia and thrombocytopenia]], [[Wiskott-Aldrich Syndrome]] | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
Line 84: | Line 108: | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Nutritional / Metabolic''' | | '''Nutritional / Metabolic''' | ||
|bgcolor="Beige"| [[B12 deficiency]], [[Folate deficiency]], [[Gaucher Disease]], [[Glycogen Storage Disease]] Type I, [[Malnutrition]], [[Niemann-Pick disease]], [[Sphingolipidosis]], [[Thiopurine S methyltranferase deficiency]], [[Von Gierke Disease]], [[Xylosylprotein 4-beta-galactosyltransferase (XGPT) deficiency | |bgcolor="Beige"| [[B12 deficiency]], [[Folate deficiency]], [[Gaucher Disease]], [[Glycogen Storage Disease]] Type I, [[Malnutrition]], [[Niemann-Pick disease]], [[Sphingolipidosis]], [[Thiopurine S methyltranferase deficiency]], [[Von Gierke Disease]], [[Xylosylprotein 4-beta-galactosyltransferase]] (XGPT) deficiency | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
Line 113: | Line 137: | ||
| '''Renal / Electrolyte''' | | '''Renal / Electrolyte''' | ||
|bgcolor="Beige"| [[Chronic renal insufficiency]], [[Fanconi syndrome]], [[Renal failure]], [[Henoch-Schonlein purpura]] | |bgcolor="Beige"| [[Chronic renal insufficiency]], [[Fanconi syndrome]], [[Renal failure]], [[Henoch-Schonlein purpura]] | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
Line 141: | Line 164: | ||
|} | |} | ||
== | ===Causes in Alphabetical Order=== | ||
{{MultiCol}} | {{MultiCol}} | ||
Line 178: | Line 201: | ||
*[[Amyloidosis]] | *[[Amyloidosis]] | ||
*[[Anticoagulant (Warfarin | *[[Anticoagulant]] ([[Warfarin]]) | ||
*[[Aplastic anemia]] | *[[Aplastic anemia]] | ||
Line 224: | Line 247: | ||
*[[Chronic viral hepatitis]] | *[[Chronic viral hepatitis]] | ||
*[[Cirrhosis | *[[Cirrhosis]] | ||
*[[Combined deficiency of Factor V and factor VIII]] | *[[Combined deficiency of Factor V and factor VIII]] | ||
Line 251: | Line 274: | ||
*[[Difethialone rodenticide poisoning]] | *[[Difethialone rodenticide poisoning]] | ||
{{ColBreak}} | {{ColBreak}} | ||
Line 258: | Line 279: | ||
*[[Diphacinone rodenticide poisoning]] | *[[Diphacinone rodenticide poisoning]] | ||
*[[Down syndrome (Acute lymphoblastic leukemia | *[[Down syndrome]] ([[Acute lymphoblastic leukemia]]) | ||
*[[Eclampsia]] | *[[Eclampsia]] | ||
Line 266: | Line 287: | ||
*[[Entacapone]] | *[[Entacapone]] | ||
*[[Epidermolysis bullosa simplex - Ogna type | *[[Epidermolysis bullosa simplex]] - Ogna type | ||
*[[Essential thrombocytopenia]] | *[[Essential thrombocytopenia]] | ||
Line 324: | Line 345: | ||
*[[Hermansky-Pudlak Syndrome]] | *[[Hermansky-Pudlak Syndrome]] | ||
*[[Human T-lymphotropic virus type 3 | *[[Human T-lymphotropic virus]] type 3 | ||
*[[Hypersplenism]] | *[[Hypersplenism]] | ||
Line 361: | Line 382: | ||
*[[Multiple myeloma]] | *[[Multiple myeloma]] | ||
{{ColBreak}} | {{ColBreak}} | ||
Line 381: | Line 399: | ||
*[[NSAIDs]] | *[[NSAIDs]] | ||
*[[Osteogenesis imperfecta Type I | *[[Osteogenesis imperfecta]] Type I | ||
*[[Osteogenesis imperfecta type IV | *[[Osteogenesis imperfecta]] type IV | ||
*[[Owren Parahemophilia]] | *[[Owren Parahemophilia]] | ||
Line 419: | Line 437: | ||
*[[Sepsis]] | *[[Sepsis]] | ||
*[[Sodium aurothiomalate (Myocrisin Injection 2% | *[[Sodium aurothiomalate]] (Myocrisin Injection 2% | ||
*[[Solar skin exposure]] | *[[Solar skin exposure]] | ||
Line 427: | Line 445: | ||
*[[Spondylometaphyseal dysplasia with combined immunodeficiency]] | *[[Spondylometaphyseal dysplasia with combined immunodeficiency]] | ||
*[[Steroid | *[[Steroid]] | ||
*[[Storage pool platelet disease]] | *[[Storage pool platelet disease]] | ||
Line 447: | Line 465: | ||
*[[Thrombocytopenia -- cerebellar hypoplasia -- short stature]] | *[[Thrombocytopenia -- cerebellar hypoplasia -- short stature]] | ||
*[[ | *[[Thrombocytopenia]] | ||
*[[Volak rodenticide poisoning]] | *[[Volak rodenticide poisoning]] | ||
Line 465: | Line 483: | ||
*[[X-linked dyserythropoietic anaemia and thrombocytopenia]] | *[[X-linked dyserythropoietic anaemia and thrombocytopenia]] | ||
*[[Xylosylprotein 4-beta-galactosyltransferase (XGPT) deficiency | *[[Xylosylprotein 4-beta-galactosyltransferase]] (XGPT) deficiency | ||
*[[Zonisamide]] | *[[Zonisamide]] | ||
{{EndMultiCol}} | {{EndMultiCol}} | ||
==References== | |||
{{reflist|2}} | |||
[[Category:Hematology]] | |||
[[Category:Medical signs]] | |||
[[Category:Symptoms]] | |||
[[Category:Signs and symptoms]] | |||
[[Category:Grammar]] | |||
{{WikiDoc Help Menu}} | |||
{{WikiDoc Sources}} |
Latest revision as of 15:01, 20 August 2015
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]
Overview
Causes
Common Causes
- Steroid use
Causes by Organ System
Causes in Alphabetical Order
|
|