KRAS Mutation in Serous Borderline Tumor of the Testis: Report of a Case and Review of the Literature
- PMID: 33062370
- PMCID: PMC7547353
- DOI: 10.1155/2020/5419707
KRAS Mutation in Serous Borderline Tumor of the Testis: Report of a Case and Review of the Literature
Abstract
Ovarian-like epithelial tumors of the testis, including serous borderline tumors, are rare entities. We report the case of a 60-year-old man with a left intratesticular mass who had a radical orchidectomy. Histologically, the tumor was identical to the ovarian counterpart showing a well-delineated cystic lesion characterized by intraluminal papillae. The papillae are lined by atypical cuboidal or ciliated cells and are associated with psammoma bodies. The tumor cells express cytokeratin 7 (CK7), cytokeratin 5-6 (CK5-6), cancer antigen 125 (CA125), estrogen (ER), progesterone (PR), Wilm's tumor gene (WT1), paired box gene 8 (PAX8), Ber-EP4, and epithelial membrane antigen (EMA). The diagnosis of a serous borderline tumor of the testis was proposed. Mutation testing using next-generation sequencing showed a Q61K KRAS gene mutation. To the best of our knowledge, this is the second case report of a serous borderline tumor of the testis with a Q61K KRAS gene mutation.
Copyright © 2020 Sarah Bouri et al.
Conflict of interest statement
The authors declare that they have no conflict of interest regarding the publication of this article.
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References
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- Ibrahim A. S., Li C., al-Jafari M. S. Borderline serous papillary tumour of the testis: a case report and review of the literature. Anticancer Research. 2012;32(11):5011–5013. - PubMed
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