Non-seminomatous germ cell tumor with bone metastasis only at diagnosis: A rare clinical presentation

K. C. Biebighauser, Jianjun Gao, Priya Rao, Gene Landon, Lance Pagliaro, Colin P.N. Dinney, Jose Karam, Neema Navai

Research output: Contribution to journalArticle

1 Scopus citations

Abstract

Bone metastasis of non-seminomatous germ cell tumors (NSGCT) of the testes is a rare event and even more uncommon at initial presentation. Generally, bone lesions are discovered in the presence of concurrent retroperitoneal lymph node or visceral disease. However, in this case, a 37 years old male complaining of a growing testicular mass was found to have isolated bone metastasis with associated caudaequina syndrome without apparent abnormal findings on initial computed tomography (CT) scans. Continued neurologic symptoms prompted further evaluation with magnetic resonance imaging (MRI), which demonstrated multiple sites of bone metastasis without evidence of retroperitoneal lymph node or visceral organ involvement. This case represents a rare clinical presentation and disease manifestation of NSGCT.

Original languageEnglish (US)
Pages (from-to)124-127
Number of pages4
JournalAsian Journal of Urology
Volume4
Issue number2
DOIs
StatePublished - Apr 1 2017

Keywords

  • Metastasis
  • Non-seminomatous
  • Testis cancer
  • Yolk sac tumor

ASJC Scopus subject areas

  • Urology

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    Biebighauser, K. C., Gao, J., Rao, P., Landon, G., Pagliaro, L., Dinney, C. P. N., Karam, J., & Navai, N. (2017). Non-seminomatous germ cell tumor with bone metastasis only at diagnosis: A rare clinical presentation. Asian Journal of Urology, 4(2), 124-127. https://doi.org/10.1016/j.ajur.2016.08.004