ArticleCureus2026
Extensive Intra-abdominal Desmoplastic Small Round Cell Tumor With Hepatic Metastases: A Report of a Rare Case.
Article in Cureus, 2026. 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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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.
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5 authors.
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Abstract
Desmoplastic small round cell tumor (DSRCT) is a rare and highly aggressive malignancy predominantly affecting young male patients, typically originating from the abdomen or pelvis, with a poor prognosis. Since the first description as a distinct clinical entity in 1989, approximately 850 cases have been reported in the literature. All cases share the chromosomal translocation t(11;22)(p13;q12), leading to the formation of the EWSR1-WT1 fusion gene. DSRCT characteristically arises in the abdomen or pelvis and carries a poor prognosis despite multimodal therapy. We report a rare and extensive case of abdominopelvic DSRCT with liver and peritoneal metastases in a 17-year-old Moroccan male, who presented with a progressive abdominal mass, pain, and hepatomegaly. The diagnosis was initially challenging due to the non-specific clinical presentation. The final diagnosis was established through liver biopsy and immunohistochemical analysis. The patient is currently undergoing treatment with a multidrug chemotherapy regimen.
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