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A rare case of thyroid haemangiosarcoma. | LitMetric

A rare case of thyroid haemangiosarcoma.

Chir Ital

Department of Surgical Science, Unit of General Surgery and Organ Transplantation, University of Parma, Via Gramsci, 14, 43100 Parma.

Published: December 2007

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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