Abstract
Introduction: We report for the first time a case of a postpubertal patient presenting with a metastatic prepubertal-type testicular teratoma. Case discussion: A 29-year-old male with a history of corrected unilateral cryptorchidism presented with progressive bilateral lower extremity edema. Imaging revealed an inferior vena cava thrombus associated with a complex mass. A left testicular ultrasound identified a solid lesion suggestive of a germ cell tumor, leading to a left radical orchiectomy, which revealed a mature pure teratoma with no evidence of germ cell neoplasia in situ (GCNIS). Excision of the retroperitoneal mass confirmed the presence of mature teratomatous elements without evidence of non-teratomatous germ cell tumor elements or cytological atypia. Fluorescence in situ hybridization (FISH) showed no evidence of gain of 12p, and next-generation sequencing showed no alterations in genes known to be associated with GCT. Conclusion: This case illustrates that pure mature teratomas lacking chromosome 12p abnormalities, GCNIS, and other dysgenetic features, occurring in postpubertal males, cannot invariably be classified into the benign prepubertal-type teratoma category. Contrary to current paradigm, in rare cases these may represent tumors with metastatic potential.
Original language | English (US) |
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Article number | 1547258 |
Journal | Frontiers in Oncology |
Volume | 15 |
DOIs | |
State | Published - 2025 |
Bibliographical note
Publisher Copyright:Copyright © 2025 Ghirardelli Smith, Tsai, Zhong, Dejban, Nelson, Dolan, Antonarakis and Murugan.
Keywords
- germ cell neoplasia in situ (GCNIS)
- germ cell tumor (GCT)
- isochromosome 12p (i12p)
- postpubertal-type teratoma
- prepubertal-type teratoma
- testicular cancer
PubMed: MeSH publication types
- Case Reports
- Journal Article