Chromosome 8 Polysomy Accounting for MYC Over-Expression in Angiosarcoma Arising as Somatic-Type Malignancy in Metastatic Teratoma. Case Report

Author:

Vargas A. Cristina123ORCID,Grimison Peter34,Joy Christopher5,Garrone Bernadette5,Bonar Fiona1,Ghahan Raha Madadi6,Davidson Trent7,Maclean Fiona M.128

Affiliation:

1. Douglass Hanly Moir Pathology, Macquarie Park, Australia

2. Kolling Institute of Medical Research, Royal North Shore Hospital, St Leonards, Australia

3. University of Sydney, Sydney, Australia

4. Chris O’Brien Lifehouse, Camperdown, Australia

5. Sullivan Nicolades Pathology, Brisbane, Australia

6. Gosford, Australia

7. Prince of Wales Hospital, Randwick, Australia

8. Macquarie University, Sydney, Australia

Abstract

MYC over-expression by immunohistochemistry (IHC) is utilised in routine pathology practice as a surrogate marker for MYC amplification, which plays a key oncogenic role in post-irradiation and chronic lymphedema-associated angiosarcoma. We present the case of a 32-year old male, who presented with high-grade angiosarcoma arising in a background of metastatic testicular teratoma. IHC for MYC showed strong nuclear expression in the angiosarcoma cells prompting the consideration of post-irradiation-induced angiosarcoma but our patient did not undergo radiotherapy. Fluorescence in-situ hybridization (FISH) excluded MYC amplification and instead showed Chromosome 8 polysomy, which accounted for the strong MYC IHC expression present, not previously described in the context of germ cell tumours. The occurrence of MYC over-expression due to polysomy illustrates a novel clinical scenario (angiosarcoma arising as somatic malignancy) where strong MYC IHC expression can be found in the absence of underlying amplification or prior radiotherapy exposure.

Publisher

SAGE Publications

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

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