ArticleUrology case reports2025
Report of a rare case of childhood adrenocortical carcinoma and literature review.
Article in Urology case reports, 2025. 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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Authors and funding
4 authors.
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Abstract
Adrenocortical carcinoma (ACC)in children is rare, and its nonspecific clinical presentation renders early diagnosis challenging. Surgery remains the primary therapeutic approach. A multidisciplinary, multimodal treatment strategy and long-term follow-up are essential to improve prognosis. A retrospective analysis was conducted on the clinical data of a child diagnosed with ACC at our hospital, including symptoms, signs, imaging findings, surgical procedures, pathological results, and postoperative follow-up, We also perform a literature review to increase disease awareness and provide references for similar clinical cases in the future.
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