2008
DOI: 10.1002/cncr.23796
|View full text |Cite
|
Sign up to set email alerts
|

Chromosomal abnormalities detected by multicolor fluorescence in situ hybridization in fine-needle aspirates from patients with small lymphocytic lymphoma are useful for predicting survival

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
22
0
3

Year Published

2010
2010
2018
2018

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 25 publications
(25 citation statements)
references
References 22 publications
(52 reference statements)
0
22
0
3
Order By: Relevance
“…29,30 The TMA technology offers the possibility to analyze simultaneously a consistent number of cases thus reducing costs and experimental variability. 21,24 To the best of our knowledge, the present study represents the most extensive analysis conducted on biopsies of patients affected by CLL/SLL.…”
Section: Discussionmentioning
confidence: 99%
See 2 more Smart Citations
“…29,30 The TMA technology offers the possibility to analyze simultaneously a consistent number of cases thus reducing costs and experimental variability. 21,24 To the best of our knowledge, the present study represents the most extensive analysis conducted on biopsies of patients affected by CLL/SLL.…”
Section: Discussionmentioning
confidence: 99%
“…30 Excluding those cases in which failure was a consequence of lack of tissue, assessable results were obtained in 86.8 to 92.8% of the cases with each single probe (Table 1) A second methodological consideration should be raised concerning patient selection for this study. As in previous studies, 23 patients with progressive disease and clinically relevant adenopathy were included in our analysis.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…1, 2). These tests provide useful information regarding clonality, or distinctive chromosomal/molecular abnormalities associated with specific entities and lymphoid cell lineages, confirming NHL diagnosis - albeit with some exceptions and limitations [5,9,10,11,12,13,14,15,16,17,18]. Classical cytogenetics include the routine analysis of G-banded chromosomes and other cytogenetic banding techniques for the study of cell structure and chromosomes.…”
Section: Cytogenetic Analysismentioning
confidence: 99%
“…This study shows possibilities of FNA in an experienced setting. Also, multicolor FISH is possible on FNA material as shown by Caraway et al [102]. In 49 out of 50 patients with CLL, they were able to obtain data on genetic aberrations, with similar prognostic impact as known from traditional studies.…”
Section: Ancilliary Techniquesmentioning
confidence: 84%