ArticleFrontiers in oncology2025
A rare Zinner syndrome combined with testicular cancer: a case report.
Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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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1 citing paper in PubMed.
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8 authors.
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Abstract
Background: Zinner syndrome is a rare congenital disorder of the urogenital system. In current reports, cases of Zinner syndrome complicated by malignant tumors are even rarer. Case description: We reported a 26-year-old male with Zinner syndrome complicated by testicular embryonal carcinoma and retroperitoneal lymph node metastasis. He received orchiectomy, chemotherapy and a retroperitoneal lymph node dissection with favorable response. Conclusions: As suggested by this rare case, Zinner syndrome may be bound up with genitourinary malignancy tumor. When diagnosing congenital disorders of the urinary system, it is essential for clinicians to take into consideration potential complications. More importantly, it is also paramount to account for the similarities and differences in diagnosis and treatment between comorbid and isolated conditions.
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