Long-term survival following aggressive surgery and radiotherapy for pelvic fibromatosis

被引:4
作者
Seoud, M
Abbas, J
Kaspar, H
Khalil, A
Geara, F
机构
[1] Amer Univ Beirut, Med Ctr, Dept Obstet, NY Off, New York, NY 10022 USA
[2] Amer Univ Beirut, Med Ctr, Dept Gynecol, New York, NY 10022 USA
[3] Amer Univ Beirut, Med Ctr, Dept Surg, New York, NY 10022 USA
[4] Amer Univ Beirut, Med Ctr, Dept Pathol, New York, NY 10022 USA
[5] Amer Univ Beirut, Med Ctr, Dept Radiotherapy, New York, NY 10022 USA
关键词
pelvic desmoid tumor; pelvic fibromatosis;
D O I
10.1111/j.1525-1438.2005.00171.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Desmoid tumors of the female pelvis are rare. The efficacy of the available treatment modalities in improving survival and decreasing recurrence remains controversial. A 32- year- old woman presented with an asymptomatic large ischeorectal mass. Computed tomography scan revealed a large tumor adherent to the pubic bone and impinging on the bladder neck and the rectum. Aggressive surgical removal of the mass including partial osteotomy of the pubic bone was followed by radiotherapy. The patient is still alive 6 years later with no evidence of disease. Aggressive surgical management followed by radiotherapy is an acceptable means of treatment of locally invasive desmoid tumor of the female pelvis.
引用
收藏
页码:1112 / 1114
页数:3
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