Sarcomatoid renal carcinoma with angiosarcomatoid component. Light macroscopic and immunohistochemical study Academic Article Article uri icon

Overview

MeSH Major

  • Face
  • Facial Bones
  • Sturge-Weber Syndrome

abstract

  • We describe a case of primary renal pelvic carcinoma which showed an unusual histologic pattern of anastomosing blood-filled channels lined by atypical cells. This angiosarcomatoid pattern merged with solid areas typical of renal carcinoma. Immunoperoxidase stains for cytokeratin and epithelial membrane antigen were positive in both the angiosarcomatoid and typical carcinomatous areas, while stains for factor VIII-related antigen and desmin were negative. Since primary renal angiosarcomas are rare neoplasms, the diagnosis of sarcomatoid renal carcinoma should be considered in primary renal neoplasms which show this angiosarcomatoid pattern.

publication date

  • January 1992

Research

keywords

  • Academic Article

Identity

Digital Object Identifier (DOI)

  • 10.1016/0090-4295(92)90396-E

PubMed ID

  • 1413363

Additional Document Info

start page

  • 381

end page

  • 4

volume

  • 40

number

  • 4