Benign Large Cell Calcifying Sertoli Cell Tumour of the Testis: A Rare Case

Authors

  • Sudip Das Gupta Department of Urology, Sir Salimullah Medical College, Dhaka, Bangladesh
  • Md Mozaharul Islam Department of Urology, Sir Salimullah Medical College, Dhaka, Bangladesh
  • Mohammad Mahfuzur Rahman Department of Urology, Sir Salimullah Medical College, Dhaka, Bangladesh
  • - Md Rasiduzzaman Department of Urology, Sir Salimullah Medical College, Dhaka, Bangladesh
  • Md Nazrul Islam Mridha Department of Urology, Sir Salimullah Medical College, Dhaka, Bangladesh
  • Sharif Mohammad Wasim Uddin Department of Urology, Sir Salimullah Medical College, Dhaka, Bangladesh
  • Md Rashedul Alam Department of Urology, Sir Salimullah Medical College, Dhaka, Bangladesh

DOI:

https://doi.org/10.3329/bju.v20i1.49612

Keywords:

LCCSCT, Carney complex, Peutz-Jeghers syndrome, Gynecomastia

Abstract

We report a case in which a 14 years old boy with feeling of heaviness of Left testis and also dragging discomfort on the same side with gynecomastia both sides. Ultrasonography showed heterogenous mixed echogenic mass lesion in left hemi scrotum-possibly Germ cell tumor either teratoma or seminoma. His hormonal status was within normal limit except Estradiol which was 150pg/ml. The mass removed by inguinal approach and histopathology confirmed the benign large cell calcifying Sertoli cell tumour (LCCSCT). The detection of LCCSCTs may indicate to an underlying genetic multiple neoplasia syndrome such as PJS or CNC. Surgery is rarely indicated and aromatase inhibitors constitute an effective treatment for those cases that are associated with gynecomastia and/or advanced skeletal age1.

Bangladesh Journal of Urology, Vol. 20, No. 1, January 2017 p.46-48

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Published

2020-10-08

How to Cite

Gupta, S. D., Islam, M. M., Rahman, M. M., Md Rasiduzzaman, .-., Mridha, M. N. I., Uddin, S. M. W., & Alam, M. R. (2020). Benign Large Cell Calcifying Sertoli Cell Tumour of the Testis: A Rare Case. Bangladesh Journal of Urology, 20(1), 46–48. https://doi.org/10.3329/bju.v20i1.49612

Issue

Vol. 20 No. 1 (2017)

Section

Case Reports