Orphanet: Acute erythroid leukemia
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Acute erythroid leukemia

Disease definition

A rare unclassified acute myeloid leukemia characterized by a proliferation of immature cells exclusively of the erythroid lineage without a significant myeloblastic component. Microscopically, the cells may be undifferentiated or proerythroblastic in appearance. Patients may present with pancytopenia with fatigue, infections, and mucocutaneous bleedings, as well as weight loss, fever, and night sweats. Prognosis is poor.

ORPHA:318

Classification level: Disorder
  • Synonym(s):
    • AML M6
    • Acute myeloid leukemia M6
    • Erythroleukemia
  • Prevalence: Unknown
  • Inheritance: Not applicable 
  • Age of onset: Adult, Childhood, Adolescent, Elderly
  • ICD-10: C94.0
  • ICD-11: 2A60.35
  • OMIM: 133180
  • UMLS: C0023440
  • MeSH: -
  • GARD: 9620
  • MedDRA: -

  A summary on this disease is available in Español (2020) Français (2020) Nederlands (2020)

Detailed information

General public

Guidelines

Disease review articles

ERN : produced/endorsed by ERN(s)
FSMR : produced/endorsed by FSMR(s)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.