Evidence map›Paper›PMID 26454445›Full record

ReviewVirchows Archiv : an international journal of pathology2016

The many faces of small B cell lymphomas with plasmacytic differentiation and the contribution of MYD88 testing.

Steven H Swerdlow, Isinsu Kuzu, Ahmet Dogan, Stephan Dirnhofer, John K C Chan, Birgitta Sander, German Ott, Luc Xerri, Leticia Quintanilla-Martinez, Elias Campo

Open access · greenAbstract readReview
In one paragraph

Review in Virchows Archiv : an international journal of pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 114 citations in OpenAlex.

  1. Review
  2. Article
  3. MYD88L265P mutation is a highly specific marker for the nonGCB/ABC DLBCL molecular subtype.Virchows Archiv : an international journal of pathology · 2026
    Article
  4. Article
  5. CCL19bioRxiv : the preprint server for biology · 2026
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Relevance of Additional Immunohistochemical Markers in the Differential Diagnosis of Small B-Cell Lymphomas: A Case-Control StudyTurkish journal of haematology : official journal of Turkish Society of Haematology · 2022
    Article
  15. Towards precision medicine in lymphoid malignancies.Journal of internal medicine · 2022
    Review
  16. Review
  17. Article
  18. Article
  19. The pathologic diagnosis of mantle cell lymphoma.Histology and histopathology · 2021
    Review
  20. Article
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

10 authors at 10 institutions in 8 countries.

Steven H SwerdlowDivision of Hematopathology, Department of Pathology, University of Pittsburgh School of Medicine, Room G-335, 200 Lothrop Street, Pittsburgh, PA, 15213, USA. swerdlowsh@upmc.edu.ORCID http://orcid.org/0000-0002-3832-3329
Isinsu KuzuDepartment of Pathology, Ankara University School of Medicine, Sihhiye, Ankara, Turkey.
Ahmet DoganHematopathology Service, Departments of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Stephan DirnhoferInstitute of Pathology, University Hospital Basel, Basel, Switzerland.
John K C ChanQueen Elizabeth Hospital, Hong Kong, SAR, China.
Birgitta SanderDepartment of Laboratory Medicine, Division of Pathology, Karolinska Institut and Karolinska University Hospital Huddinge, Stockholm, Sweden.
German OttDepartment of Clinical Pathology, Robert-Bosch-Hospital and Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.
Luc XerriDepartment of Bio-Pathology, Institut Paoli-Calmettes and Aix-Marseille University, Marseille, France.
Leticia Quintanilla-MartinezInstitute of Pathology and Neuropathology, Eberhard Karls University of Tübingen and Comprehensive Cancer Center, University Hospital Tübingen, Tübingen, Germany.
Elias CampoHospital Clinic, University of Barcelona, Barcelona, Spain.
Aix-Marseille Université · FRAnkara University · TRKarolinska University Hospital · SEMemorial Sloan Kettering Cancer Center · USQueen Elizabeth Hospital · CNRobert Bosch Hospital · DEUniversitat de Barcelona · ESUniversity Hospital of Basel · CHUniversity of Pittsburgh · USUniversity of Tübingen · DE

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Plasmacytic differentiation may occur in almost all small B cell lymphomas (SBLs), although it varies from being uniformly present (as in lymphoplasmacytic lymphoma (LPL)) to very uncommon (as in mantle cell lymphomas (MCLs)). The discovery of MYD88 L265P mutations in the vast majority of LPLs has had a major impact on the study of these lymphomas. Review of the cases contributed to the 2014 European Association for Haematopathology/Society for Hematopathology slide workshop illustrated how mutational testing has helped refine the diagnostic criteria for LPL, emphasizing the importance of identifying a clonal monotonous lymphoplasmacytic population and highlighting how LPL can still be diagnosed with extensive nodal architectural effacement, very subtle plasmacytic differentiation, follicular colonization, or uncommon phenotypes such as CD5 or CD10 expression. MYD88 L265P mutations were found in 11/11 LPL cases versus only 2 of 28 other SBLs included in its differential diagnosis. Mutational testing also helped to exclude other cases that would have been considered LPL in the past. The workshop also highlighted how plasmacytic differentiation can occur in chronic lymphocytic leukemia/small lymphocytic lymphoma, follicular lymphoma, SOX11 negative MCL, and particularly in marginal zone lymphomas, all of which can cause diagnostic confusion with LPL. The cases also highlighted the difficulty in distinguishing lymphomas with marked plasmacytic differentiation from plasma cell neoplasms. Some SBLs with plasmacytic differentiation can be associated with amyloid, other immunoglobulin deposition, or crystal-storing histiocytosis, which may obscure the underlying neoplasm. Finally, although generally indolent, LPL may transform, with the workshop cases suggesting a role for TP53 abnormalities.

Indexed as

AnimalsHematopoiesisHumansLymphoma, B-Cell, Marginal ZoneLymphoma, FollicularLymphoma, Mantle-CellMyeloid Differentiation Factor 88Waldenstrom MacroglobulinemiaMyeloid Differentiation Factor 88Chronic lymphocytic leukemiaFollicular lymphomaLymphoplasmacytic lymphomaMantle cell lymphomaMarginal zone lymphomaMYD88Plasmacytic differentiation

Identifiers

PMID26454445
PMCPMC5002945
OpenAlexW1917406824

What OpenQuestion holds

Textmetadata
LicenceTDM
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.