Cargando…
Recurrent isochromosome 21 and multiple abnormalities in a patient suspected of having acute myeloid leukemia with eosinophilic differentiation—a rare case from South India
Acute myeloid leukemia (AML) is a phenotypically heterogeneous disorder. The M4 subtype of AML is frequently associated with the cytogenetic marker inversion 16 and/or the presence of eosinophilia. Blast crisis is the aggressive phase of the triphasic chronic myeloid leukemia (CML), which is a disea...
Autores principales: | Vijay, Sangeetha, Sarojam, Santhi, Raveendran, Sureshkumar, Syamala, Vani, Leelakumari, Sreeja, Narayanan, Geetha, Hariharan, Sreedharan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sun Yat-sen University Cancer Center
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777464/ https://www.ncbi.nlm.nih.gov/pubmed/22176774 http://dx.doi.org/10.5732/cjc.011.10201 |
Ejemplares similares
-
A novel chromosomal abnormality t (9;14)(p24;q13) in B-acute lymphoblastic leukemia
por: Raveendran, Sureshkumar, et al.
Publicado: (2014) -
Novel t(7;10)(p22;p24) along with NPM1 mutation in patient with relapsed acute myeloid leukemia
por: Sarojam, Santhi, et al.
Publicado: (2013) -
Enigmatic Inv(9): A Case Report on Rare Findings in Hematological Malignancies
por: Vijay, Sangeetha, et al.
Publicado: (2016) -
Significance of nucleophosmin1 (NPM1) gene mutation status on acute myeloid leukaemia patients with normal karyotype in South India
por: Sureshkumar, R, et al.
Publicado: (2014) -
Turner Syndrome With Isochromosome Structural Abnormalities: A Case Report
por: Ferdousi, Tahmina, et al.
Publicado: (2023)