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ArticleVirchows Archiv : an international journal of pathology2026

Renal hemangioblastoma and renal cell carcinoma with fibromyomatous stroma and hemangioblastoma-like areas belong to the spectrum of one entity.

Kiril Trpkov, Norel Salut, Inmaculada Ribera-Cortada, Elías Tasso Xipell, Isabel Trias Puigsureda, Asli Yilmaz, Arjumand Riyaz Husain, Erik Nohr, Adrian Box, Farshid Siadat and 5 more

Abstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Hemangioblastoma of the Kidney-A Comprehensive Clinical, Pathological, and Genetic Analysis of Four Cases.APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 2026
    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

15 authors.

Kiril TrpkovDiagnostic and Molecular Pathology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada. kiril.trpkov@albertaprecisionlabs.ca.ORCID http://orcid.org/0000-0003-3142-8846
Norel SalutDiagnostic and Molecular Pathology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.ORCID http://orcid.org/0009-0006-8343-4294
Inmaculada Ribera-CortadaDepartment of Pathology, Hospital Clínic of Barcelona, University of Barcelona, 08036, Barcelona, Spain.ORCID http://orcid.org/0000-0002-3372-828X
Elías Tasso XipellDepartment of Pathology, Hospital Clínic of Barcelona, University of Barcelona, 08036, Barcelona, Spain.ORCID http://orcid.org/0009-0009-8532-4998
Isabel Trias PuigsuredaDepartment of Pathology, Hospital Clínic of Barcelona, University of Barcelona, 08036, Barcelona, Spain.ORCID http://orcid.org/0000-0001-9841-4380
Asli YilmazDiagnostic and Molecular Pathology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Arjumand Riyaz HusainDiagnostic and Molecular Pathology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Erik NohrDiagnostic and Molecular Pathology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Adrian BoxDiagnostic and Molecular Pathology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Farshid SiadatDiagnostic and Molecular Pathology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.ORCID http://orcid.org/0000-0001-7676-4806
Katherina BaranovaDepartment of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON, Canada.ORCID http://orcid.org/0000-0003-4740-9789
Rola M SaleebDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-1937-3101
Robert StoehrInstitute of Pathology, Comprehensive Cancer Center, Erlangen University Hospital, Friedrich Alexander University of Erlangen-Nuremberg, European Metropolitan Area Erlangen-Nuremberg (CCC ER-EMN), Erlangen, Germany.
Arndt HartmannInstitute of Pathology, Comprehensive Cancer Center, Erlangen University Hospital, Friedrich Alexander University of Erlangen-Nuremberg, European Metropolitan Area Erlangen-Nuremberg (CCC ER-EMN), Erlangen, Germany.ORCID http://orcid.org/0000-0002-4860-4626
Abbas AgaimyInstitute of Pathology, Comprehensive Cancer Center, Erlangen University Hospital, Friedrich Alexander University of Erlangen-Nuremberg, European Metropolitan Area Erlangen-Nuremberg (CCC ER-EMN), Erlangen, Germany.ORCID http://orcid.org/0000-0002-0445-8161

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several reports have documented renal cell carcinomas (RCC) with fibromyomatous stroma and with areas of hemangioblastoma (RCC FMS-HB). The hemangioblastoma component in RCC FMS-HB tumors was similar to the morphology of primary renal hemangioblastoma, suggesting that RCC FMS-HB and renal hemangioblastoma share common features. Seven study cases were collected, comprised of three RCC FMS-HB (two sporadic and one in a tuberous sclerosis patient) and four pure renal hemangioblastomas. A molecular analysis was successful in 6/7 cases. There were four males and three females, with an age range of 27 to 74 years, and a mean age of 51 years. The tumors measured from 2.6 to 5.5 cm (median 3.5 cm), and all were organ-confined, stage pT1. Median size for RCC FMS-HB was 2.8 cm, and for renal hemangioblastoma, it was 3.5 cm. The hemangioblastoma component in all RCC FMS-HBs and in all renal hemangioblastomas was positive for inhibin-α and S100 but was negative for CK7. In contrast, the clear-cell epithelial component in RCC FMS-HB was diffusely reactive for CK7 and was negative for inhibin-α and S100. Both components were reactive for CAIX, vimentin, and GPNMB. TSC/MTOR pathway alterations were found in 6/6 successfully evaluated cases, including 3/3 RCC FMS-HB and 3/3 renal hemangioblastomas, with mutations in TSC1 (2/6), TSC2 (2/6), and MTOR (2/6). The shared morphologic, immunohistochemical, and molecular features of RCC FMS-HB and renal hemangioblastoma indicate that they belong to a common biological spectrum, and that renal HB is a distinct entity from its VHL-altered central nervous system counterpart.

Indexed as

Carcinoma, Renal CellHemangioblastomaKidney NeoplasmsAdultAgedBiomarkers, TumorFemaleHumansImmunohistochemistryMaleMiddle AgedTuberous SclerosisBiomarkers, TumorClear cellFibromyomatous stromaHemangioblastomaKidneyRenal cell carcinoma (RCC)TSC/MTOR

Identifiers

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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.