Evidence map›Paper›PMID 41323049›Full record

ArticleCase reports in oncology

Small Desmoplastic Round Cell Tumor of the Kidney following Hodgkin Lymphoma: Case Report and Literature Review.

Aaron Rosenfeld, Sarah Blain, Kyoko Yuki, Nisha Kanwar, Anita Villani, Brianna Empringham, Lesleigh S Abbott

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Case reports in oncology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Aaron RosenfeldDepartment of Pediatrics, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Sarah BlainDepartment of Pediatrics, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
Kyoko YukiDepartment of Pediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, ON, Canada.
Nisha KanwarDepartment of Pediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, ON, Canada.
Anita VillaniDepartment of Pediatrics, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Brianna EmpringhamDepartment of Pediatrics, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
Lesleigh S AbbottDepartment of Pediatrics, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Desmoplastic small round cell tumor (DSRCT) is a rare and aggressive sarcoma that is most commonly present in males with abdominal and peritoneal invasion. There are potential curative therapeutic options, but survival remains poor. To this day, there have only been 22 reported cases of primary renal DSRCT in the literature and thoracic DSRCT has been rarely reported with very little known about effective therapy. This is the first reported case of renal DSRCT following a primary malignancy, and it is further distinguished by the application of whole-genome sequencing and targeted biological therapy. Case Presentation: The literature on renal DSRCT was reviewed, and we describe a patient with thoracic relapse of DSRCT following a primary renal lesion, initially treated with radical nephrectomy and 14 cycles of chemotherapy (doxorubicin 225 mg/m Conclusion: DSRCT remains a highly aggressive malignancy with limited treatment options and poor prognosis. Our case highlights the rarity of primary renal DSRCT and its potential for thoracic relapse, further emphasizing the challenges in disease management.

Indexed as

Pediatric oncologyRenal massSoft tissue sarcoma

Identifiers

PMID41323049
PMCPMC12659638

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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.