NIGHT PAROXYSTIC HEMOGLOBINURIA

Authors

  • Víctor Andrés García Rojas Residente de Medicina Interna. Hospital México CCSS. Sistema de Estudios de Posgrado Universidad de Costa Rica
  • Xinia Alexandra Sánchez Vargas Residente de Medicina Interna. Hospital México CCSS. Sistema de Estudios de Posgrado Universidad de Costa Rica
  • Gustavo Adolfo Mora Hernández Residente de Medicina Interna. Hospital México CCSS. Sistema de Estudios de Posgrado Universidad de Costa Rica

Keywords:

Paroxysmal nocturnal hemoglobinuria, Microangiopathic hemolytic anemia

Abstract

Paroxysmal nocturnal hemoglobinuria is a rare acquired chronic hemolytic anemia, which affects both sexes with equal frequency. It occurs at any age and more frequently in Southeast Asian countries. It is the result of non malignant clonal expansion of hematopoietic progenitor cells. It is characterized by intravascular hemolytic anemia, recurrent thrombosis and a variable component of bone marrow failure. It is associated with other hematologic disorders such as aplastic anemia and myelodysplastic syndrome. Flow cytometry is the method of choice for diagnosis. Eculizumab and allogeneic bone marrow transplantation is the only effective therapies.

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Published

2020-11-12

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