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High Grade Leiomyosarcoma Mimicking a Recurrent Angiomyxoma in the Perineum.
Sood, Neha; Swaika, Abhisek; Hanooshi, Bashar; Waldorf, James; Peterson, Jennifer; Wu, Kevin; Attia, Steven; Dinh, Tri A.
Afiliação
  • Sood N; Department of Medical and Surgical Gynecology, Mayo Clinic Florida , Jacksonville, FL, USA.
  • Swaika A; Department of Medicine, Mayo Clinic Florida , Jacksonville, FL, USA.
  • Hanooshi B; Department of Obstetrics and Gynecology, Flushing Hospital Medical Center , New York City, NY, USA.
  • Waldorf J; Department of Plastic Surgery, Mayo Clinic Florida , Jacksonville, FL, USA.
  • Peterson J; Department of Radiation Oncology, Mayo Clinic Florida , Jacksonville, FL, USA.
  • Wu K; Department of Pathology, Mayo Clinic Florida , Jacksonville, FL, USA.
  • Attia S; Department of Medicine, Mayo Clinic Florida , Jacksonville, FL, USA.
  • Dinh TA; Department of Medical and Surgical Gynecology, Mayo Clinic Florida , Jacksonville, FL, USA.
Rare Tumors ; 7(2): 5875, 2015 May 05.
Article em En | MEDLINE | ID: mdl-26266017
Perineal leiomyosarcoma is an extremely rare and aggressive cancer with a high metastatic potential and no defined standard treatment. There are only a few (six) reported cases in the literature. We report the case of a 67-year-old woman with a perineal leiomyosarcoma arising at the same site of a previously resected superficial angiomyxoma. Initially, she was treated for a presumptive recurrence of angiomyxoma. As she did not respond to medical therapy, she underwent repeat surgical excision. Pathology revealed a high grade leiomyosarcoma, histologically strikingly distinct from the initial diagnosis. She received adjuvant local radiation therapy, and remains without evidence of recurrent disease 36 months after completion of all therapy. This is the first reported case of a high grade perineal leiomyosarcoma originating at the same site as a resected benign superficial angiomyxoma. Our case emphasizes the necessity of a prompt histological diagnosis in cases of presumed recurrent perineal angiomyxoma.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Rare Tumors Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Rare Tumors Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos