Pure Leydig cell tumor: a rare case report
Abstract
Leydig cell tumors are rare tumors and constitute 1-3% of all testicular tumors. The pure form of these tumors, which are often found in mixed form with sertoli cells, is extremely rare. It is very difficult to determine the malignancy potential in leydig cell tumors most commonly manifested by a testicular mass or endocrine symptoms. In this study, clinical, histological and prognostic features of a pure form of Leydig cell tumors are presented in the light of literature information.
Keywords
References
- 1. Dilworth JP, Farrow GM, Oesterling JE. Non-germ cell tumors of testis. Urology 1991; 37: 399–417.
- 2. Emerson RE, Ulbright TM: Morphological approach to tumours of the testis and paratestis. J Clin Pathol 2007; 60: 866–80.
- 3. Cheville JC: Classification and pathology of testicular germ cell and sex cord-stromal tumors. Urol Clin North Am 1999; 26: 595–609.
- 4. Leonhartsberger N, Ramoner R, Aigner F, et al. Increased incidence of Leydig cell tumours of the testis in the era of improved imaging techniques. BJU Int 2011; 108: 1603–07.
- 5. Giacaglia LR, Kohek MB da F, Carvalho FM, Fragoso MC, Mendonca B, Latronico AC. No evidence of somatic activating mutations on gonadotropin receptor genes in sex cord stromal tumors. Fertil Steril 2000; 74: 992–5.
- 6. Libe R, Fratticci A, Lahlou N, et al. A rare cause of hypertestosteronemia in a 68-year-old patient: a Leydig cell tumor due to a somatic GNAS (guanine nucleotide-binding protein, alpha-stimulating activity polypeptide 1)-activating mutation. J Androl 2012; 33: 578–84.
- 7. Carvajal-Carmona LG, Alam NA, Pollard PJ, et al. Adult leydig cell tumors of the testis caused by germline fumarate hydratase mutations. J Clin Endocrinol Metab 2006; 91: 3071–5.
- 8. Lejeune H, Habert R, Saez JM. Origin, proliferation and differentiation of Leydig cells. J Mol Endocrinol 1998, 20: 1–25.
Details
Primary Language
English
Subjects
Health Care Administration
Journal Section
Case Report
Authors
Mehmet Zengin
*
Türkiye
Publication Date
April 1, 2019
Submission Date
August 14, 2018
Acceptance Date
September 16, 2018
Published in Issue
Year 2019 Volume: 2 Number: 2











