DOAJ Open Access 2025

A rare case of metachronous pituitary germinoma and testicular seminoma: The role of tumor markers in diagnosis and the influence of glucocorticoids on disease progression

Rachel Sheskier Parisa Verma Alexander Kirschenbaum Bella Orelowitz Melissa Umphlett +5 lainnya

Abstrak

The presence of both an extragonadal germ cell tumor and gonadal germ cell tumor is a rare occurrence with few cases reported in the literature. We herein report a case of a young man presenting with hypophysitis due to a pituitary germinoma. After a course of high dose glucocorticoid (GC) therapy and the surgical removal of the germinoma, a testicular seminoma was discovered, an apparently second distinct primary germ cell tumor. Hypophysitis was initially attributed to lymphocytic hypophysitis due to the largely unrevealing secondary work up that included beta-human chorionic gonadotropin (b-hCG) and alpha fetoprotein (AFP), which highlights the pitfalls of relying on the tumor marker of b-hCG in both germinomas and seminomas and the important role of biopsy for definitive diagnosis of hypophysitis etiology. Furthermore, the presentation of the seminoma following a course of high dose GC indicates that immunosuppressive therapies may promote the growth of these germ cell tumors.

Penulis (10)

R

Rachel Sheskier

P

Parisa Verma

A

Alexander Kirschenbaum

B

Bella Orelowitz

M

Melissa Umphlett

U

Umar Sharif

J

John Sfakianos

L

Leslie Schlachter

J

Joshua Bederson

A

Alice C. Levine

Format Sitasi

Sheskier, R., Verma, P., Kirschenbaum, A., Orelowitz, B., Umphlett, M., Sharif, U. et al. (2025). A rare case of metachronous pituitary germinoma and testicular seminoma: The role of tumor markers in diagnosis and the influence of glucocorticoids on disease progression. https://doi.org/10.1016/j.jecr.2025.100182

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Informasi Jurnal
Tahun Terbit
2025
Sumber Database
DOAJ
DOI
10.1016/j.jecr.2025.100182
Akses
Open Access ✓