Evidence map›Paper›PMID 37958219›Full record

ReviewDiagnostics (Basel, Switzerland)2023

Diagnostic Approach to Pulmonary B-Cell Lymphomas in Small Biopsies, with Practical Recommendations to Avoid Misinterpretation.

Sergio Pina-Oviedo, Victor L Roggli, Thomas A Sporn, Huihua Li, Carolyn Glass, Louis R DiBernardo, Elizabeth N Pavlisko

Open access · goldAbstract readReview
In one paragraph

Review in Diagnostics (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

7 authors at 1 institution in 1 country.

Sergio Pina-OviedoDepartment of Pathology, Duke University Medical Center, Durham, NC 27710-4000, USA.ORCID 0000-0002-0987-0251
Victor L RoggliDepartment of Pathology, Duke University Medical Center, Durham, NC 27710-4000, USA.
Thomas A SpornDepartment of Pathology, Duke University Medical Center, Durham, NC 27710-4000, USA.
Huihua LiDepartment of Pathology, Duke University Medical Center, Durham, NC 27710-4000, USA.ORCID 0009-0009-7725-407X
Carolyn GlassDepartment of Pathology, Duke University Medical Center, Durham, NC 27710-4000, USA.
Louis R DiBernardoDepartment of Pathology, Duke University Medical Center, Durham, NC 27710-4000, USA.ORCID 0009-0001-4391-6778
Elizabeth N PavliskoDepartment of Pathology, Duke University Medical Center, Durham, NC 27710-4000, USA.
Duke Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary lymphomas are rare. With the current less invasive approaches used to obtain material for diagnosis, the diagnosis of pulmonary lymphoma is now frequently established in a small biopsy rather than in a resection. Therefore, the diagnosis has become more challenging and requires correlation with the clinico-radiologic presentation and with ancillary studies (immunohistochemistry, flow cytometry, cytogenetics, and/or molecular analysis). Due to the rarity of pulmonary lymphomas, clinical suspicion of a lymphomatous process is low at initial presentation, and material may be only submitted for histopathology. For this reason, herein, we provide recommendations to arrive at the correct diagnosis of the most common lung B-cell lymphomas (marginal zone lymphoma of mucosa-associated lymphoid tissue, diffuse large B-cell lymphoma, intravascular large B-cell lymphoma, lymphomatoid granulomatosis) in the setting of small biopsies, utilizing only immunohistochemistry. The differential diagnosis varies according to the lymphoma subtype and includes reactive conditions, solid tumors, and other hematolymphoid malignancies. Although morphology and immunohistochemistry may be sufficient to establish a diagnosis, in some cases, the best recommendation is to obtain additional tissue via a VATS biopsy/wedge resection with material submitted for flow cytometry, cytogenetics, and/or molecular studies to be able to properly classify a pulmonary lymphoid process.

Indexed as

differential diagnosisDLBCLextranodal lymphomaimmunohistochemistryintravascular lymphomalymphomatoid granulomatosisMALT lymphomanodular lymphoid hyperplasia

Identifiers

PMID37958219
PMCPMC10650405
OpenAlexW4387971552

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.