Cargando…
A case report of T-LGL leukemia-associated pure red cell aplasia harboring STAT3, TNFAIP3, and KMT2D mutation
BACKGROUND: T-large granular lymphocyte (T-LGL) leukemia is a rare clonal lymphoproliferative disorder, which has a favorable prognosis. There are different complications between Asian and Western patients diagnosed with LGL leukemia. In Asians, pure red cell aplasia (PRCA) is the most common hemato...
Autor principal: | Shen, Meixiao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174971/ https://www.ncbi.nlm.nih.gov/pubmed/37180665 http://dx.doi.org/10.21037/tcr-23-326 |
Ejemplares similares
-
STAT3 gene mutations and their association with pure red cell aplasia in large granular lymphocyte leukemia
por: Ishida, Fumihiro, et al.
Publicado: (2014) -
STAT3 mutations are frequent in T-cell large granular lymphocytic leukemia with pure red cell aplasia
por: Qiu, Zhi-Yuan, et al.
Publicado: (2013) -
Emergence of a STAT3 mutated NK clone in LGL leukemia
por: Yan, Yiyi, et al.
Publicado: (2014) -
STAT3 mutation impacts biological and clinical features of T-LGL leukemia
por: Teramo, Antonella, et al.
Publicado: (2017) -
Distinct mutational pattern of T-cell large granular lymphocyte leukemia combined with pure red cell aplasia: low mutational burden of STAT3
por: Park, Sooyong, et al.
Publicado: (2023)