Evidence map›Paper›PMID 40762649›Full record

ReviewVirchows Archiv : an international journal of pathology2025

Diagnosing the silent: the molecular landscape of non-functional parathyroid carcinoma.

Maaia Margo Jentus, Willem E Corver, Marieke Snel, Femke M van Haalen, Tom van Wezel, Dina Ruano, Ellen Kapiteijn, Stijn Crobach, Natasha M Appelman-Dijkstra, Abbey Schepers and 1 more

Abstract readCase ReportsReview
In one paragraph

Review in Virchows Archiv : an international journal of pathology, 2025. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

11 authors.

Maaia Margo JentusDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands. m.jentus@lumc.nl.ORCID http://orcid.org/0000-0001-5724-7643
Willem E CorverDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Marieke SnelDepartment of Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, The Netherlands.
Femke M van HaalenDepartment of Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, The Netherlands.
Tom van WezelDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Dina RuanoDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Ellen KapiteijnDepartment of Medical Oncology, Leiden University Medical Center, Leiden, The Netherlands.
Stijn CrobachDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Natasha M Appelman-DijkstraDepartment of Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, The Netherlands.
Abbey SchepersDepartment of Surgery, Leiden University Medical Center, Leiden, The Netherlands.
Hans MorreauDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-functional parathyroid carcinoma (NFPC) is an exceptionally rare malignancy, with approximately 50 cases reported since the parathyroid glands were first described in the late nineteenth century. Unlike functional parathyroid carcinomas (PC), which typically present with severe hyperparathyroidism (HPT) and are monitored via serum calcium and parathyroid hormone (PTH) levels, NFPC lacks biochemical markers and is monitored solely through imaging. In this study, we present two new cases of primary NFPC and provide a comprehensive review of the literature, including a detailed analysis of immunohistochemical and molecular testing. We also explore potential mechanisms underlying the non-functional state in PC. In one case, the tumor lacked PTH expression by immunohistochemistry, yet low levels of PTH mRNA expression were consistently detected. Differential diagnoses-including medullary and non-medullary thyroid carcinoma, paraganglioma, and other head and neck tumors-were excluded. The second case demonstrated patchy residual PTH immunostaining. Both tumors exhibited extensive whole chromosome losses resulting in a near-haploid genome, with (NFPC 2) or without (NFPC 1) subsequent endoreduplication/genome doubling. The mutational landscape differed between the two, with neither showing CDC73 mutations or loss of parafibromin expression. Diagnosing primary non-functional parathyroid carcinoma can be especially challenging in cases with negative PTH immunohistochemistry.

Indexed as

Biomarkers, TumorCarcinomaParathyroid NeoplasmsHumansImmunohistochemistryMutationParathyroid HormoneTumor Suppressor ProteinsBiomarkers, TumorCDC73 protein, humanParathyroid HormoneTumor Suppressor ProteinsEndocrine pathologyMolecular analysisNon-functional parathyroid carcinomaParathyroidParathyroid carcinomaParathyroid neoplasiaRare cancerWhole chromosome loss

Identifiers

PMID40762649
PMCPMC12748313

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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.