| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5681485 | Medicine - Programa de Formación Médica Continuada Acreditado | 2016 | 5 Pages |
Abstract
The diagnosis of HA is based on a careful clinical history, with emphasis on family antecedents, physical examination to recognize the hemolytic syndrome, and the typical laboratory findings with regenerative anemia, increased indirect bilirubin and decreased haptoglobin in blood. In the etiologic diagnosis a Coombs test and the morphological study of peripheral blood smear by an expert hematologist are essential. The presence of schistocytes suggests the diagnosis of Microangiopathic HA that requires urgent treatment.
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Authors
V. Cabañas Perianes, M. Berenguer Piqueras, E. Salido Fiérrez, J.M. Moraleda Jiménez,