Carcinoma of the Thyroid With Ewing Family Tumor Elements and Favorable Prognosis: Report of a Second Case

First Published May 1, 2013 Case Report Find in PubMed

Authors

, MD,PhD123
 
Centro Hospitalar de São João, Porto, Portugal
 
IPATIMUP (Institute of Molecular Pathology and Immunology of the University of Porto), Porto, Portugal
 
University of Porto, Porto, Portugal
by this author
, , MD4
 
Centro Hospitalar de Lisboa Central, Lisboa, Portugal
by this author
, , MSc5
 
Portuguese Oncology Institute, Porto, Portugal
by this author
,
, MD PhD35
 
University of Porto, Porto, Portugal
 
Portuguese Oncology Institute, Porto, Portugal
by this author
, , MD6
 
Hospital CUF Descobertas, Lisboa, Portugal
by this author
, , MD PhD123
 
Centro Hospitalar de São João, Porto, Portugal
 
IPATIMUP (Institute of Molecular Pathology and Immunology of the University of Porto), Porto, Portugal
 
University of Porto, Porto, Portugal
by this author
...
First Published Online: May 1, 2013

The rare reports of primary, nonneuroendocrine small cell carcinomas of the thyroid have not provided enough evidence to support the recognition of these tumors as an entity or to understand their etiopathogenesis. We report the second case of a primary, nonneuroendocrine small cell carcinoma of the thyroid displaying diffuse expression of cytokeratins, CD99, and p63, in the absence of vimentin expression, in a 24-year-old male who is alive without any signs of disease 13 years after total thyroidectomy and radioactive iodine. The tumor disclosed the EWSR1-FLI1 rearrangement, and we propose to designate it as a carcinoma of the thyroid with Ewing family tumor elements.

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