Thyroid angiosarcoma (TAS) - A rare diagnosis not to be missed.
Autor: | Kehagias D; Department of General Surgery University Hospital of Patras Rio Greece., Kostopoulou E; Division of Pediatric Endocrinology Department of Pediatrics University Hospital of Patras Rio Greece., Ravazoula P; Department of Pathology University Hospital of Patras Rio Greece., Panagopoulos K; Department of General Surgery University Hospital of Patras Rio Greece. |
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Jazyk: | angličtina |
Zdroj: | Clinical case reports [Clin Case Rep] 2020 Nov 11; Vol. 9 (1), pp. 173-176. Date of Electronic Publication: 2020 Nov 11 (Print Publication: 2021). |
DOI: | 10.1002/ccr3.3492 |
Abstrakt: | Raising awareness about primary TAS, a rare and aggressive mesenchymal tumor, is important so that early diagnosis and undelayed radical surgery along with complementary radiation are possible. Extending the existing knowledge on the course and final outcome of the disease may help identify the best treatment approach to improve survival. Competing Interests: The authors declare that they have no competing interests. (© 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.) |
Databáze: | MEDLINE |
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