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

Virchows Arch. 1999 Jul;435(1):62-6. doi: 10.1007/s004280050396.

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 1.5x2x2.5 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.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Aorta, Thoracic / pathology*
  • Aortic Aneurysm / complications
  • Biomarkers, Tumor / metabolism
  • Cell Differentiation
  • Humans
  • Male
  • Microscopy, Electron
  • Rhabdomyosarcoma / complications
  • Rhabdomyosarcoma / metabolism
  • Rhabdomyosarcoma / pathology*
  • Rhabdomyosarcoma / ultrastructure
  • Sarcoma / complications
  • Sarcoma / diagnostic imaging
  • Sarcoma / metabolism
  • Sarcoma / pathology*
  • Sarcoma / ultrastructure
  • Tomography, X-Ray Computed
  • Tunica Intima / pathology*
  • Vascular Neoplasms / complications
  • Vascular Neoplasms / metabolism
  • Vascular Neoplasms / pathology*
  • Vascular Neoplasms / ultrastructure

Substances

  • Biomarkers, Tumor