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Angiosarcomas in chronically lymphedematous extremities. Two cases of Stewart-Treves syndrome.

Abstract
Two cases of Stewart-Treves syndrome are presented. The first case consists of an angiosarcoma developing in long-standing postmastectomy lymphedema. The second case has an unusual localization on the lower extremity. The results of immunohistochemical stainings with Factor VIII-related antigen, UEA-1 lectin, and laminin support the assumption that Stewart-Treves syndrome is a hemangioendotheliosarcoma.
AuthorsB M Hultberg
JournalThe American Journal of dermatopathology (Am J Dermatopathol) Vol. 9 Issue 5 Pg. 406-12 (Oct 1987) ISSN: 0193-1091 [Print] United States
PMID3120612 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Antigens
  • Laminin
  • Lectins
  • Plant Lectins
  • Ulex europaeus lectins
  • von Willebrand Factor
  • Factor VIII
Topics
  • Adult
  • Aged
  • Antigens (analysis)
  • Arm
  • Factor VIII (analysis, immunology)
  • Female
  • Hemangiosarcoma (immunology, ultrastructure)
  • Humans
  • Immunoenzyme Techniques
  • Knee
  • Laminin (analysis)
  • Lectins (analysis)
  • Lymphedema (physiopathology)
  • Neoplasm Recurrence, Local (ultrastructure)
  • Neoplasms, Multiple Primary (ultrastructure)
  • Plant Lectins
  • Skin Neoplasms (immunology, ultrastructure)
  • Syndrome
  • von Willebrand Factor

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