Myelodysplastic syndrome terminating in erythropoietic protoporphyria after 15 years of aplastic anemia.
Int J Hematol
; 72(1): 44-7, 2000 Jul.
Article
en En
| MEDLINE
| ID: mdl-10979208
ABSTRACT
The authors report a case of aplastic anemia in which refractory anemia, a subtype of myelodysplastic syndrome (MDS), developed 15 years after the onset and was subsequently followed by erythropoietic protoporphyria (EPP). Defects of stem cells in MDS are thought to be responsible for the disturbance of the heme biosynthetic pathway, leading to the development of EPP.
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Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Síndromes Mielodisplásicos
/
Porfiria Hepatoeritropoyética
/
Anemia Aplásica
Tipo de estudio:
Diagnostic_studies
/
Etiology_studies
Límite:
Female
/
Humans
/
Middle aged
País/Región como asunto:
Asia
Idioma:
En
Revista:
Int J Hematol
Asunto de la revista:
HEMATOLOGIA
Año:
2000
Tipo del documento:
Article
País de afiliación:
Japón