Disease | purpura |
Phenotype | C0002878|hemolytic anemia |
Sentences | 3 |
PubMedID- 23823096 | [successful rituximab treatment for acquired amegakaryocytic thrombocytopenic purpura complicated with coombs-negative autoimmune hemolytic anemia]. |
PubMedID- 22374533 | Based on these data, we initially suspected evan's syndrome, which involves idiopathic thrombocytopenic purpura with autoimmune hemolytic anemia. |
PubMedID- 22708045 | The differential diagnosis included microangiopathic hemolytic anemia (maha) associated with thrombotic thrombocytopenic purpura (ttp)/hemolytic-uremic syndrome (hus), systemic inflammatory response syndrome (sirs), antiphospholipid antibody syndrome, a compensated disseminated intravascular coagulation (dic), and /or hypertension-associated maha. |
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