Evidence map›Paper›PMID 35203531›Full record

ReviewBiomedicines2022

TSC/mTOR Pathway Mutation Associated Eosinophilic/Oncocytic Renal Neoplasms: A Heterogeneous Group of Tumors with Distinct Morphology, Immunohistochemical Profile, and Similar Genetic Background.

Kristyna Pivovarcikova, Reza Alaghehbandan, Tomas Vanecek, Riuko Ohashi, Tomas Pitra, Ondrej Hes

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Observational
  8. Review
  9. Article
  10. Renal Cell Carcinoma in End-Stage Renal Disease: A Retrospective Study in Patients from Hungary.Pathobiology : journal of immunopathology, molecular and cellular biology · 2023
    Article
  11. 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

6 authors at 3 institutions in 3 countries.

Kristyna PivovarcikovaDepartment of Pathology, Faculty of Medicine in Pilsen, University Hospital Pilsen, Charles University in Prague, 30460 Pilsen, Czech Republic.
Reza AlaghehbandanDepartment of Pathology, Faculty of Medicine, University of British Columbia, Royal Columbian Hospital, Vancouver, BC V3L 3W7, Canada.
Tomas VanecekDepartment of Pathology, Faculty of Medicine in Pilsen, University Hospital Pilsen, Charles University in Prague, 30460 Pilsen, Czech Republic.
Riuko OhashiHistopathology Core Facility, Niigata University Faculty of Medicine, 1-757 Asahimachi-dori, Chuo-ku, Niigata 951-8510, Japan.ORCID 0000-0001-5820-7870
Tomas PitraDepartment of Urology, Faculty of Medicine in Pilsen, University Hospital Pilsen, Charles University in Prague, 30599 Pilsen, Czech Republic.ORCID 0000-0001-7367-5832
Ondrej HesDepartment of Pathology, Faculty of Medicine in Pilsen, University Hospital Pilsen, Charles University in Prague, 30460 Pilsen, Czech Republic.
Charles University · CZNiigata University · JPRoyal Columbian Hospital · CA

Funding

Charles University Research Fund project number Q39Ministry of Education, Czech Republic SVV 260539Ministry of Health of the Czech republic-Conceptual Development of Research Organization Faculty Hospital in Plzen- FNPl 00669806
6 · The paper itself

Abstract

A number of recently described renal tumor entities share an eosinophilic/oncocytic morphology, somewhat solid architectural growth pattern, and tendency to present as low-stage tumors. The vast majority of such tumors follow a non-aggressive clinical behavior. In this review, we discuss the morphological, immunohistochemical, and molecular genetic profiles of the three most recent novel/emerging renal entities associated with TSC/mTOR pathway mutations. These are eosinophilic solid and cystic renal cell carcinoma, eosinophilic vacuolated tumors, and low-grade oncocytic tumors, which belong to a heterogeneous group of renal tumors, demonstrating mostly solid architecture, eosinophilic/oncocytic cytoplasm, and overlapping morphological and immunohistochemical features between renal oncocytoma and chromophobe renal cell carcinoma. All three tumors also share a molecular genetic background with mutations in the mTORC1 pathway (

Indexed as

chromophobeeosinophilicESCEVTkidneyLOTmTORoncocyticrenaltumor

Identifiers

PMID35203531
PMCPMC8869370
OpenAlexW4210712271

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.