Evidence map›Paper›PMID 26991267›Full record

ArticlePloS one2016

Isolated Follicles Enriched for Centroblasts and Lacking t(14;18)/BCL2 in Lymphoid Tissue: Diagnostic and Clinical Implications.

Grant E Nybakken, Rajeev Bala, Dita Gratzinger, Carol D Jones, James L Zehnder, Charles D Bangs, Athena Cherry, Roger A Warnke, Yasodha Natkunam

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Grant E NybakkenDepartment of Pathology, Stanford University School of Medicine, Stanford, California, 94305, United States of America.
Rajeev BalaDepartment of Pathology, Stanford University School of Medicine, Stanford, California, 94305, United States of America.
Dita GratzingerDepartment of Pathology, Stanford University School of Medicine, Stanford, California, 94305, United States of America.
Carol D JonesDepartment of Pathology, Stanford University School of Medicine, Stanford, California, 94305, United States of America.
James L ZehnderDepartment of Pathology, Stanford University School of Medicine, Stanford, California, 94305, United States of America.
Charles D BangsDepartment of Pathology, Stanford University School of Medicine, Stanford, California, 94305, United States of America.
Athena CherryDepartment of Pathology, Stanford University School of Medicine, Stanford, California, 94305, United States of America.
Roger A WarnkeDepartment of Pathology, Stanford University School of Medicine, Stanford, California, 94305, United States of America.
Yasodha NatkunamDepartment of Pathology, Stanford University School of Medicine, Stanford, California, 94305, United States of America.
Stanford University · US

Funding

TUMOR SPECIFIC CYTOTOXIC T-LYMPHOCYTES IN BONE MARROW TRANSPLANTATIONP01CA049605 · NCI · STANFORD UNIVERSITY · PI David B. Miklos · 1989 to 2026
$73.3M
NCI NIH HHS P01 CA049605
6 · The paper itself

Abstract

We sought to address the significance of isolated follicles that exhibit atypical morphologic features that may be mistaken for lymphoma in a background of reactive lymphoid tissue. Seven cases that demonstrated centroblast-predominant isolated follicles and absent BCL2 staining in otherwise-normal lymph nodes were studied. Four of seven cases showed clonal B-cell proliferations amid a polyclonal B cell background; all cases lacked the IGH-BCL2 translocation and BCL2 protein expression. Although three patients had invasive breast carcinoma at other sites, none were associated with systemic lymphoma up to 44 months after diagnosis. The immunoarchitectural features of these highly unusual cases raise the question of whether a predominance of centroblasts and/or absence of BCL2 expression could represent a precursor lesion or atypical reactive phenomenon. Differentiating such cases from follicular lymphoma or another mimic is critical, lest patients with indolent proliferations be exposed to unnecessarily aggressive treatment.

Indexed as

B-LymphocytesBreast NeoplasmsCell ProliferationChildChromosomes, Human, Pair 14Chromosomes, Human, Pair 18FemaleHumansImmunoglobulin kappa-ChainsImmunoglobulin lambda-ChainsIn Situ Hybridization, FluorescenceLymph NodesLymphoma, FollicularMaleMiddle AgedPolymerase Chain ReactionImmunoglobulin kappa-ChainsImmunoglobulin lambda-ChainsProto-Oncogene Proteins c-bcl-2

Identifiers

PMID26991267
PMCPMC4798531
OpenAlexW2318582825

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.