Toggle Main Menu Toggle Search

Open Access padlockePrints

The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Hyperthyroidism in non-seminomatous testicular germ cell tumors: two case reports and literature review

Lookup NU author(s): Dr Christoph OingORCiD, Dr Pasquale RescignoORCiD

Downloads


Licence

This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

Copyright © 2024 Favero, Oing, Seidel, Rescigno, Catalano, Cremante, Rebuzzi, Gatto, Rosti, Ferone, Fornarini and Cocchiara. Background: Human chorionic gonadotropin (hCG)–induced hyperthyroidism is a rare paraneoplastic syndrome observed in non-seminomatous testicular germ cell tumors, due to a cross-reaction between the β-subunit of hCG with the thyroid-stimulating hormone receptor. The precise prevalence of this paraneoplastic phenomenon is unclear as, in the majority of cases, hyperthyroidism remains subclinical. Case presentation: Here, we present two cases of advanced metastatic non-seminomatous testicular germ cell tumors where patients exhibited signs and symptoms of thyrotoxicosis at primary diagnosis due to excessive serum β-hCG elevation, with complete remission of symptomatology after the start of oncological treatments and no signs of relapse at the time of publication of this report. Additionally, we provide a comprehensive review of the existing literature concerning this uncommon occurrence. Conclusion: Despite being a rare event, the presence of hyperthyroidism or thyrotoxicosis without clear etiology in a young man should lead to consider less frequent causes such as testicular tumors. Even if patients typically have mild symptoms that resolve after chemotherapy, in rare cases, it can be a life-threatening condition that requires prompt recognition and specific intervention.


Publication metadata

Author(s): Favero D, Oing C, Seidel C, Rescigno P, Catalano F, Cremante M, Rebuzzi SE, Gatto F, Rosti G, Ferone D, Fornarini G, Cocchiara F

Publication type: Article

Publication status: Published

Journal: Frontiers in Oncology

Year: 2024

Volume: 14

Online publication date: 27/03/2024

Acceptance date: 26/02/2024

Date deposited: 24/07/2024

ISSN (electronic): 2234-943X

Publisher: Frontiers Media SA

URL: https://doi.org/10.3389/fonc.2024.1338438

DOI: 10.3389/fonc.2024.1338438

Data Access Statement: The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.


Altmetrics

Altmetrics provided by Altmetric


Share