Evidence map›Paper›PMID 42844928›Full record

ArticlePathology international2026

Pleural Mesothelioma With Unusual Squamous Differentiation: A Clinicopathological Case Report With Molecular Insights From Whole-Exome Sequencing.

Julius Bodemeyer, Mara Elisa Mierzwa, Jörg Seraphin, Rizkallah Maroun, Wolfgang Körber, Christoph Engelke, Felix Bremmer, Tessa Rosenthal, Tim Heißenberg, Kirsten Reuter-Jessen and 3 more

Abstract readCase Reports
In one paragraph

Article in Pathology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

13 authors.

Julius BodemeyerInstitute of Pathology, University Medical Center, Göttingen, Germany.ORCID https://orcid.org/0000-0001-9937-1837
Mara Elisa MierzwaInstitute of Pathology, University Medical Center, Göttingen, Germany.
Jörg SeraphinMedical Care Center Onkologikum Northeim, Northeim, Germany.
Rizkallah MarounMedical Care Center Onkologikum Northeim, Northeim, Germany.
Wolfgang KörberDepartment for Pneumology, Evangelical Hospital Göttingen-Weende, Göttingen, Germany.
Christoph EngelkeDepartment for Radiology, Evangelical Hospital Göttingen-Weende, Göttingen, Germany.
Felix BremmerInstitute of Pathology, University Medical Center, Göttingen, Germany.ORCID https://orcid.org/0000-0003-0367-6527
Tessa RosenthalInstitute of Pathology, University Medical Center, Göttingen, Germany.
Tim HeißenbergDepartment of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
Kirsten Reuter-JessenInstitute of Pathology, University Medical Center, Göttingen, Germany.
Philipp StröbelInstitute of Pathology, University Medical Center, Göttingen, Germany.ORCID https://orcid.org/0000-0002-8528-8060
Alexander MarxInstitute of Pathology, University Medical Center, Göttingen, Germany.
Hanibal BohnenbergerInstitute of Pathology, University Medical Center, Göttingen, Germany.ORCID https://orcid.org/0000-0003-1038-1030

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pleural mesothelioma is an aggressive tumor with a poor prognosis and limited therapeutic options. While histological heterogeneity is common, true squamous differentiation is extremely rare and diagnostically challenging. We report an 81-year-old man with asbestos exposure who presented with recurrent right-sided pleural effusion. Thoracoscopic biopsies revealed two distinct tumor components. The first expressed mesothelial immunohistochemical markers, whereas the second showed a squamous profile. Both components demonstrated loss of BAP1 expression and homozygous deletion of CDKN2A, supporting a common mesothelial origin. Whole-exome sequencing revealed a tumor mutational burden above the average reported for mesothelioma (8-9 mutations per megabase), with 69 somatic mutations in total, 43 shared between the two components. In addition to canonical mesothelioma alterations (BAP1, CHEK2), the squamous component harbored 18 unique variants, including oncogenic alterations in NFE2L2 and PIK3CA. A novel SOX9 missense variant of uncertain significance (p. Thr243Pro) was also identified within the transactivation middle (TAM) domain; its functional consequence remains unknown. This case highlights a rare histological variant of pleural mesothelioma with partially squamous differentiation, characterized by a mutational burden above the mesothelioma average and squamous carcinoma-associated alterations. Integrated histology, immunohistochemistry, and genomic profiling are essential to avoid misdiagnosis and to improve understanding of tumor plasticity in mesothelioma.

Indexed as

Carcinoma, Squamous CellLung NeoplasmsMesotheliomaPleural NeoplasmsAged, 80 and overBiomarkers, TumorCell DifferentiationExome SequencingHumansMaleMesothelioma, MalignantMutationBiomarkers, Tumordifferential diagnosismesotheliomasquamous transdifferentiationwhole‐exome sequencing

Identifiers

PMID42844928
PMCPMC13646670

What OpenQuestion holds

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Registered trials

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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.