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Research Article| Volume 11, ISSUE 5, P744-748, September 1986

Malignant fibrous histiocytoma in a child's hand

  • A. Bullon
    Affiliations
    Plastic and Reconstructive Surgery Department, Madrid, Spain

    Pathology Department, La Paz Hospital, School of Medicine, Autonomous University, Madrid, Spain
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  • M. Nistal
    Correspondence
    Reprint requests: Manuel Nistal, M. D., Departamento de Morfologia, Facultad de Medicina, Universidad Autónoma, Cl Arzobispo Morcillo 2, 28029-Madrid, Spain.
    Affiliations
    Plastic and Reconstructive Surgery Department, Madrid, Spain

    Pathology Department, La Paz Hospital, School of Medicine, Autonomous University, Madrid, Spain
    Search for articles by this author
  • S. Razquin
    Affiliations
    Plastic and Reconstructive Surgery Department, Madrid, Spain

    Pathology Department, La Paz Hospital, School of Medicine, Autonomous University, Madrid, Spain
    Search for articles by this author
  • A. Novo
    Affiliations
    Plastic and Reconstructive Surgery Department, Madrid, Spain

    Pathology Department, La Paz Hospital, School of Medicine, Autonomous University, Madrid, Spain
    Search for articles by this author
  • J. Fregenal
    Affiliations
    Plastic and Reconstructive Surgery Department, Madrid, Spain

    Pathology Department, La Paz Hospital, School of Medicine, Autonomous University, Madrid, Spain
    Search for articles by this author
  • J. Regadera
    Affiliations
    Plastic and Reconstructive Surgery Department, Madrid, Spain

    Pathology Department, La Paz Hospital, School of Medicine, Autonomous University, Madrid, Spain
    Search for articles by this author
      This paper is only available as a PDF. To read, Please Download here.
      A 3-year-old girl had a 4-month history of a tumor in her right hand. The tumor was located in the subcutaneous and soft tissues of the palm and the long, ring, and small fingers. Histologic studies showed a malignant fibrous histiocytoma that was confirmed by the ultrastructural study as having a fibroblastic and histiocytic origin. The long, ring, and small fingers were amputated. The postoperative course was normal, and 18 months later no recurrence or metastases were observed.
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