Publication: Next-generation sequencing-based characterization of the invasion by anatomical contiguity in a primary osseous diffuse large B-cell lymphoma. Correlation between the genetic profile of the malignancy and the clinical outcome of the patient
Authors
Zaharie, Florin ; Pop, Laura-Ancuta ; Petrushev, Bobe ; Jurj, Ancuta ; Muresan, Mihai-Stefan ; Eniu, Dan ; Fetica, Bogdan ; Petkov, Bozhidar ; Pasca, Sergiu ; Piciu, Doina ; Rus, Ioana ; Deak, Dalma ; Dima, Delia ; Desmirean, Minodora-Silvia ; Tomuleasa, Ciprian ; Berindan-Neagoe, Ioana
item.page.secondaryauthor
item.page.director
Publisher
Universidad de Murcia. Departamento de BiologĂa Celular e HistologĂa
publication.page.editor
publication.page.department
DOI
DOI: 10.14670/HH-18-067
item.page.type
info:eu-repo/semantics/article
Description
Abstract
Primary bone lymphoma is now a welldescribed entity in the World Health Organization
(WHO) Classification of Tumors of Soft Tissue and
Bone as a malignancy of the lymphoid tissue, with at
least one mass within bone, without involvement of
supraregional lymph nodes or other extranodal sites. In
the current paper, we describe the complete
characterization of the mutational landscape of a diffuse
large B cell non-Hodgkin's lymphoma (DLBLCL) of the
tibial plateau. Currently, there is very little data about the
genetic landscape of primary osseous lymphomas and
about the genetic background of this type of malignancy,
resistant to chemotherapy and invading the surrounding
tissues. In the current paper, we describe the complete
characterization of the mutational landscape of a
DLBCL of the tibial plateau. Our data is consistent with
already published data, that have shown that MKI67
activation is correlated with lymphoma progression.
Along with a high Ki67 index, resistance to
chemotherapy occurs with neurogenic locus notch
homolog protein 1 (Notch) and KRAS activation.
This is the first molecular characterization for the
invasion by anatomical contiguity for a primary bone
lymphoma and while we only characterized one case and
further deep sequencing analyses are required, we can
explain the clinical dismal evolution of the patient by
correlating them with the genetic landscape of this type
of lymphoma.
publication.page.subject
Citation
Histology and Histopathology, Vol.34, nÂş6, (2019)
item.page.embargo
Ir a EstadĂsticas
Este Ătem está sujeto a una licencia Creative Commons. http://creativecommons.org/licenses/by-nc-nd/4.0/