Evidence map›Paper›PMID 36832239›Full record

ArticleDiagnostics (Basel, Switzerland)2023

A Primary Kidney Giant Cell Tumor of Soft Tissue Caused Peritoneal Dissemination, Considered to Be Malignant Transformation: A Case Report.

Chiina Hata, Yuki Fukawa, Toru Motoi, Yuko Kinowaki, Takumi Akashi, Kenichi Ohashi, Yudai Ishikawa, Yuma Waseda, Yasuhisa Fujii, Ryota Kakuta and 2 more

Open access · goldAbstract readCase Reports
In one paragraph

Article 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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Giant Cell Tumor of Soft Tissue: An Updated Review.Journal of clinical medicine · 2024
    Review
  3. Review
  4. 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

12 authors at 3 institutions in 1 country.

Chiina HataDepartment of Human Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.ORCID 0000-0001-9692-4328
Yuki FukawaDepartment of Oral Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.ORCID 0000-0002-7538-4251
Toru MotoiDepartment of Pathology, Tokyo Metropolitan Cancer and Infectious Disease Center, Komagome Hospital, Tokyo 113-8677, Japan.ORCID 0000-0002-3597-7730
Yuko KinowakiDepartment of Comprehensive Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.ORCID 0000-0001-8907-2569
Takumi AkashiDepartment of Diagnostic Pathology, Tokyo Medical and Dental University Hospital, Tokyo 113-8510, Japan.
Kenichi OhashiDepartment of Human Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.
Yudai IshikawaDepartment of Urology, Tokyo Medical and Dental University Hospital, Tokyo 113-8510, Japan.ORCID 0000-0001-7118-5522
Yuma WasedaDepartment of Urology, Tokyo Medical and Dental University Hospital, Tokyo 113-8510, Japan.ORCID 0000-0002-9319-1373
Yasuhisa FujiiDepartment of Urology, Tokyo Medical and Dental University Hospital, Tokyo 113-8510, Japan.
Ryota KakutaDepartment of Clinical Oncology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.
Sadakatsu IkedaDepartment of Clinical Oncology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.
Iichiroh OnishiDepartment of Diagnostic Pathology, Tokyo Medical and Dental University Hospital, Tokyo 113-8510, Japan.ORCID 0000-0001-9744-0114
Tokyo Medical and Dental University · JPTokyo Medical and Dental University Hospital · JPTokyo Metropolitan Komagome Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Giant cell tumor of soft tissue (GCTST) is a defined disease entity that has a morphology similar to giant cell tumor of bone (GCTB). The malignant transformation of GCTST has not been reported, and a kidney primary is extremely rare. We report the case of a 77-year-old Japanese male, who was diagnosed with primary GCTST of the kidney and showed peritoneal dissemination, considered to be a malignant transformation of GCTST, in 4 years and 5 months. Histologically, the primary lesion showed characteristics of round cells with not prominent atypia, multi-nucleated giant cells, and osteoid formation, and carcinoma components were not found. The peritoneal lesion was characterized by osteoid formation and round to spindle-shaped cells, but differed in nuclear atypia, and multi-nucleated giant cells were not detected. Immunohistochemical and cancer genome sequence analysis suggested these tumors were sequential. This is a first report of a case that we could diagnose as primary GCTST of the kidney and could be determined as malignant transformation of GCTST in the clinical course. Analysis of this case will be examined in the future when genetic mutations and the disease concepts of GCTST are established.

Indexed as

giant cell tumor of soft tissuekidneymalignant transformation

Identifiers

PMID36832239
PMCPMC9955081
OpenAlexW4321090566

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.