Caspian Journal of Internal Medicine
Babol University of Medical Sciences
Wed, Mar 19, 2025
[Archive]
Volume 14, Issue 1 (Winter 2023)
Caspian J Intern Med 2023, 14(1): 147-149 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Emadi Torghabeh A, Dovlati M, Gharib M, Saghafi H, Saghafi M. Primary carcinoid or sex cord-stromal tumor of the testis. A case report. Caspian J Intern Med 2023; 14 (1) :147-149
URL: http://caspjim.com/article-1-2697-en.html
URL: http://caspjim.com/article-1-2697-en.html
Ali Emadi Torghabeh 
, Mahmoud Dovlati , Masoumeh Gharib , Hamidreza Saghafi , Mohammadreza Saghafi *
, Mahmoud Dovlati , Masoumeh Gharib , Hamidreza Saghafi , Mohammadreza Saghafi *
Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran , imansaghafi86@gmail.com
Abstract: (1940 Views)
Background: Carcinoid tumors of the testis are rare and orchiectomy is the preferred treatment. This type of testis tumors is rare and their differentiation from sex cord-stromal tumors is difficult.
Case presentation: A 29‑year‑old man presented with right testicular mass and underwent radical orchidectomy. Histological examination showed neuroendocrine tumor, confirmed by immunohistochemistry and electron microscopy (Ethic code: IR.MUMS.REC.1400.237).
Conclusion: Primary testicular neuroendocrine tumor is very rare. It is crucial to submit the entire gross specimen for histopathologic examination to rule out an existing of other germ cell elements. Our patient had a well-differentiated carcinoid tumor and after two years of follow-up (every three months), there was no recurrence or metastasis.
Case presentation: A 29‑year‑old man presented with right testicular mass and underwent radical orchidectomy. Histological examination showed neuroendocrine tumor, confirmed by immunohistochemistry and electron microscopy (Ethic code: IR.MUMS.REC.1400.237).
Conclusion: Primary testicular neuroendocrine tumor is very rare. It is crucial to submit the entire gross specimen for histopathologic examination to rule out an existing of other germ cell elements. Our patient had a well-differentiated carcinoid tumor and after two years of follow-up (every three months), there was no recurrence or metastasis.
Keywords: neuroendocrine tumor, sex cord-stromal tumor of the testis, testicular cancer Leydig, Sertoli, and granulosa cells, testicular swelling
Type of Study: case report |
Subject:
Oncology
Received: 2021/01/7 | Accepted: 2021/12/13 | Published: 2023/01/11
Received: 2021/01/7 | Accepted: 2021/12/13 | Published: 2023/01/11
Send email to the article author
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
