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Published on: June 9, 2023
A rare case of thyroid haemangiosarcoma
Paolo Del Rio1, Simona Cataldo, Lucia Sommaruga
1Department of Surgical Science, Unit of General Surgery and Organ Transplantation, University of Parma, Via Gramsci, 14, 43100 Parma.
Abstract:
The incidence of haemangiosarcoma in the literature is variable especially in the Alpine region and in Austria, ranging from 2 to 10% of all thyroid neoplastic lesions. This thyroid disease is characterised by positive endothelial markers (CD 31, CD 34 and FVIII), and co-positive markers for cytokeratins, epithelial membrane antigen and a loss of thyroglobulin can sometimes be found. Immunochemistry does not help the physician to classify the neoplasia as a variant of anaplastic carcinoma or sarcoma of endothelial origin. We present a case of epithelioid haemangiosarcoma in an elderly woman from outside the Alpine region with a contralateral papillary cancer treated by total thyroidectomy. The prognosis is poor and case reports are rare.
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