Intimal-type primary sarcoma of the aorta - Report of a case with evidenceof rhabdomyosarcomatous differentiation

Citation
C. Miracco et al., Intimal-type primary sarcoma of the aorta - Report of a case with evidenceof rhabdomyosarcomatous differentiation, VIRCHOWS AR, 435(1), 1999, pp. 62-66
Citations number
30
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
ISSN journal
09456317 → ACNP
Volume
435
Issue
1
Year of publication
1999
Pages
62 - 66
Database
ISI
SICI code
0945-6317(199907)435:1<62:IPSOTA>2.0.ZU;2-1
Abstract
We report an intimal sarcoma presenting as an aortic aneurysm. A 68-year-ol d man suffered from chest pain and speech disturbance. Computed tomography showed a sacciform aneurysm of the aorta, which was resected, revealing a p olypoid tumour measuring 1.5x2x2.5 cm projecting into the lumen. This prove d to be a poorly differentiated high-grade sarcoma having morphological, im munophenotypic and ultrastructural features consistent with rhabdomyosarcom atous differentiation. Primary sarcomas of the aorta are extremely rare. Ma ny cases have been diagnosed as "intimal" on the basis of their site of ori gin, and they are not easy to classify from their histological pattern. Ele ctron microscopy and the use of a more comprehensive panel of immunohistoch emical markers should be applied in the histological classification of "int imal" sarcoma.