Scheithauer Bernd W, Silva Ana Isabel, Kattner Keith, Seibly Jason, Oliveira Andre M, Kovacs Kalman
Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First St., SW, Rochester, MN 55905, USA.
Neuro Oncol. 2007 Oct;9(4):454-9. doi: 10.1215/15228517-2007-029. Epub 2007 Aug 17.
Primary sarcomas of the sellar region are uncommon, although a wide variety have been reported. To date, no cases of primary synovial sarcoma have been described as occurring at this site. We report an immunohistochemically and molecular genetically confirmed primary synovial sarcoma involving the sellar/parasellar region and cavernous sinus in an adult male. Subtotal resection and radiosurgery proved to be efficacious. The spectrum of primary sellar region sarcomas is summarized.
鞍区原发性肉瘤并不常见，尽管已有多种类型的报道。迄今为止，尚无原发性滑膜肉瘤发生于此部位的病例描述。我们报告一例经免疫组织化学和分子遗传学证实的成年男性原发性滑膜肉瘤，累及鞍区/鞍旁区域及海绵窦。次全切除和放射外科治疗证明是有效的。本文总结了原发性鞍区肉瘤的谱系。
