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Case Reports
. 2020 Sep 30:2020:5419707.
doi: 10.1155/2020/5419707. eCollection 2020.

KRAS Mutation in Serous Borderline Tumor of the Testis: Report of a Case and Review of the Literature

Affiliations
Case Reports

KRAS Mutation in Serous Borderline Tumor of the Testis: Report of a Case and Review of the Literature

Sarah Bouri et al. Case Rep Urol. .

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.

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Conflict of interest statement

The authors declare that they have no conflict of interest regarding the publication of this article.

Figures

Figure 1
Figure 1
Ultrasound features: heterogenous, hypoechogenic, and cystic tumor of 20 mm.
Figure 2
Figure 2
Macroscopically, the intratesticular tumor appeared cystic with an endoluminal solid area.
Figure 3
Figure 3
Microscopic view: cystic tumor with papillae lined by pseudo- or pluristratified atypical epithelium (hematoxylin and eosin) (×10).

References

    1. 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
    1. Maruyama H., Ohyama N., Hosokawa Y., et al. Serous borderline tumor of the paratestis. Pathology International. 2008;58(5):311–316. doi: 10.1111/j.1440-1827.2008.02229.x. - DOI - PubMed
    1. Abdullah L. S., Gupta R., Arnst A. Intratesticular borderline serous tumor. International Journal of Urology. 2006;13(12):1536–1538. doi: 10.1111/j.1442-2042.2006.01575.x. - DOI - PubMed
    1. McClure R. F., Keeney G. L., Sebo T. J., Cheville J. C. Serous borderline tumor of the paratestis: a report of seven cases. The American Journal of Surgical Pathology. 2001;25(3):373–378. doi: 10.1097/00000478-200103000-00012. - DOI - PubMed
    1. Guarch R., Rivas A., Puras A., Pesce C. Papillary serous carcinoma of ovarian type of the testis with borderline differentiation. Histopathology. 2005;46(5):588–590. doi: 10.1111/j.1365-2559.2005.02017.x. - DOI - PubMed

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