Progress of diagnosis and treatment of acute mixed-cell leukemia / 白血病·淋巴瘤
Journal of Leukemia & Lymphoma
; (12): 634-636, 2017.
Article
in Chinese
| WPRIM (Western Pacific)
| ID: wpr-661195
Responsible library:
WPRO
ABSTRACT
Acute mixed-cell leukemia (MPAL) is a rare high-risk leukemia that may originate from pluripotent hematopoietic stem cells.At present,the pathogenesis of MPAL is not clear,which mainly relys on immunophenotyping and molecular genetic diagnosis. Allogeneic hematopoietic stem cell transplantation may be the only way to cure the disease, depending on the immunophenotype and genetic characteristics of the leptin and/or myeloid induction chemotherapy. The prognosis of MPAL is worse than that of other acute leukemia, and understanding of these phenotypic genetic related clinical changes, biological significances and its pathogenesis will help to prevent and treat this disease effectively.
Full text:
Available
Database:
WPRIM (Western Pacific)
Type of study:
Diagnostic study
/
Prognostic study
Language:
Chinese
Journal:
Journal of Leukemia & Lymphoma
Year:
2017
Document type:
Article