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Intimal-type primary sarcoma of the aorta

Report of a case with evidence of rhabdomyosarcomatous differentiation

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Abstract

 We report an intimal sarcoma presenting as an aortic aneurysm. A 68-year-old man suffered from chest pain and speech disturbance. Computed tomography showed a sacciform aneurysm of the aorta, which was resected, revealing a polypoid tumour measuring 1.5×2×2.5 cm projecting into the lumen. This proved to be a poorly differentiated high-grade sarcoma having morphological, immunophenotypic and ultrastructural features consistent with rhabdomyosarcomatous differentiation. Primary sarcomas of the aorta are extremely rare. Many cases have been diagnosed as ”intimal” on the basis of their site of origin, and they are not easy to classify from their histological pattern. Electron microscopy and the use of a more comprehensive panel of immunohistochemical markers should be applied in the histological classification of ”intimal” sarcoma.

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Received: 18 January 1999 / Accepted: 24 February 1999

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Miracco, C., Laurini, L., Santopietro, R. et al. Intimal-type primary sarcoma of the aorta . Virchows Archiv 435, 62–66 (1999). https://doi.org/10.1007/s004280050396

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  • DOI: https://doi.org/10.1007/s004280050396

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