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PedAM

Pediatric Disease Annotations & Medicines




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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