Hemophilic pelvic pseudotumor

Sandra Castro-Boix, Jordi Pradell-Teigell, Ramón Boqué-Genovard, Vicente Zanón-Navarro, Antoni Nadal-Guinard, Carme Altisent-Roca, Manel Armengol-Carrasco

Research output: Contribution to journalArticleResearchpeer-review

9 Citations (Scopus)

Abstract

Surgery in hemophilic patients is a challenge for the general surgeon. Hemophilic pseudotumor is a rare complication occurring in 1-2% of hemophiliacs and affecting mainly patients with severe disease or those who have developed antibodies to factor VIII or IX. A number of alternatives are available for the management of these tumors, including conservative treatment, surgical removal, percutaneous drainage, embolization, and external radiation. The only definitive treatment is surgical excision. We report a case of hemophilic pseudotumor of the pelvic bone. Treatment consisted of surgical resection after arterial embolization using factor replacement to achieve hemostasis.
Original languageEnglish
Pages (from-to)102-104
JournalCirugia Espanola
Volume81
Issue number2
DOIs
Publication statusPublished - 1 Feb 2007

Keywords

  • Embolization
  • Factor IX
  • Hemophilia B
  • Surgery
  • Surgical hemostasis

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