ArticleCureus2025
Juvenile Granulosa Cell Tumor in an Adolescent With Xeroderma Pigmentosum: A Rare Case and Implications for Surveillance.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
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.
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Who cites it
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We report the case of a 14-year-old girl with xeroderma pigmentosum who was incidentally found to have a juvenile granulosa cell tumor of the ovary during routine imaging. The tumor was surgically removed, and no signs of hormonal activity or metastasis were observed. The patient had an uneventful recovery and required no additional therapy. This case underscores a rare but noteworthy association between a DNA repair disorder and early-onset gynecological tumors, highlighting the importance of regular gynecological surveillance in affected patients. Early detection may improve clinical outcomes and reduce the need for aggressive treatment.
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Registered trials
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.