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Testicular cancer in Down syndrome with spinal cord metastases

A 22-year-old male patient with Down syndrome was referred to our hospital with a vast left testicular mass. He underwent a left radical inguinal orchiectomy, and a histopathological examination of the mass showed a yolk sac tumor invading the epididymis. The patient was discharged in a satisfactory...

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Autores principales: Almouhissen, Turky, Badr, Hattan, AlMatrafi, Bassam, Alessa, Noor, Nassir, Anmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100165/
https://www.ncbi.nlm.nih.gov/pubmed/28058004
http://dx.doi.org/10.4103/0974-7796.192109
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author Almouhissen, Turky
Badr, Hattan
AlMatrafi, Bassam
Alessa, Noor
Nassir, Anmar
author_facet Almouhissen, Turky
Badr, Hattan
AlMatrafi, Bassam
Alessa, Noor
Nassir, Anmar
author_sort Almouhissen, Turky
collection PubMed
description A 22-year-old male patient with Down syndrome was referred to our hospital with a vast left testicular mass. He underwent a left radical inguinal orchiectomy, and a histopathological examination of the mass showed a yolk sac tumor invading the epididymis. The patient was discharged in a satisfactory condition. Sixteen days later, the patient presented again complaining of lower limb weakness. Magnetic resonance imaging of the spine showed metastatic lesions compressing the dorsal spine, and he underwent emergency surgical decompression. The histopathology of the metastatic lesions revealed a yolk sac subtype which was identical to his primary testicular tumor.
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spelling pubmed-51001652017-01-05 Testicular cancer in Down syndrome with spinal cord metastases Almouhissen, Turky Badr, Hattan AlMatrafi, Bassam Alessa, Noor Nassir, Anmar Urol Ann Case Report A 22-year-old male patient with Down syndrome was referred to our hospital with a vast left testicular mass. He underwent a left radical inguinal orchiectomy, and a histopathological examination of the mass showed a yolk sac tumor invading the epididymis. The patient was discharged in a satisfactory condition. Sixteen days later, the patient presented again complaining of lower limb weakness. Magnetic resonance imaging of the spine showed metastatic lesions compressing the dorsal spine, and he underwent emergency surgical decompression. The histopathology of the metastatic lesions revealed a yolk sac subtype which was identical to his primary testicular tumor. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC5100165/ /pubmed/28058004 http://dx.doi.org/10.4103/0974-7796.192109 Text en Copyright: © Urology Annals http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Almouhissen, Turky
Badr, Hattan
AlMatrafi, Bassam
Alessa, Noor
Nassir, Anmar
Testicular cancer in Down syndrome with spinal cord metastases
title Testicular cancer in Down syndrome with spinal cord metastases
title_full Testicular cancer in Down syndrome with spinal cord metastases
title_fullStr Testicular cancer in Down syndrome with spinal cord metastases
title_full_unstemmed Testicular cancer in Down syndrome with spinal cord metastases
title_short Testicular cancer in Down syndrome with spinal cord metastases
title_sort testicular cancer in down syndrome with spinal cord metastases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100165/
https://www.ncbi.nlm.nih.gov/pubmed/28058004
http://dx.doi.org/10.4103/0974-7796.192109
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AT almatrafibassam testicularcancerindownsyndromewithspinalcordmetastases
AT alessanoor testicularcancerindownsyndromewithspinalcordmetastases
AT nassiranmar testicularcancerindownsyndromewithspinalcordmetastases