Disease | hemolytic anemia |
Phenotype | C0034150|purpura |
Sentences | 5 |
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. |
PubMedID- 22374533 | Based on these data, we initially suspected evan's syndrome, which involves idiopathic thrombocytopenic purpura with autoimmune hemolytic anemia. |
PubMedID- 22574558 | The patient was diagnosed thrombotic thrombocytopenic purpura (ttp) following pentad of clinical features: microangiopathic hemolytic anemia, thrombocytopenia, fever neurologic, and renal abnormalities. |
PubMedID- 22833609 | Because the patient had fever, purpura, laboratory evidence of hemolytic anemia and kidney failure, b. microti infection was suspected and subsequently confirmed by blood smear, serology, rodent inoculation and polymerase chain reaction (pcr) among other molecular methods as outlined in the results and discussion section. |
PubMedID- 23823096 | [successful rituximab treatment for acquired amegakaryocytic thrombocytopenic purpura complicated with coombs-negative autoimmune hemolytic anemia]. |
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