Small bowel leiomyosarcoma: A case report and literature review

被引:8
|
作者
Arts, Rob [1 ]
Bosscha, Koop [1 ]
Ranschaert, Erik [2 ]
Vogelaar, Jeroen [1 ]
机构
[1] Jeroen Bosch Hosp, Dept Surg, Shertogenbosch, Netherlands
[2] Jeroen Bosch Hosp, Dept Radiol, Shertogenbosch, Netherlands
来源
TURKISH JOURNAL OF GASTROENTEROLOGY | 2012年 / 23卷 / 04期
关键词
Leiomyosarcoma; small intestine neoplasms; small bowel tumors; jejunal neoplasms; jejunal tumors; GASTROINTESTINAL STROMAL TUMORS; SOFT-TISSUE SARCOMAS; RANDOMIZED PHASE-II; EUROPEAN ORGANIZATION; MALIGNANT-TUMORS; CANCER; GEMCITABINE; IFOSFAMIDE; LEIOMYOMAS; DOCETAXEL;
D O I
10.4318/tjg.2012.0406
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Small bowel neoplasms are very uncommon, especially leiomyosarcoma of the small bowel. Therefore, there is often a delay before small bowel leiomyosarcoma is diagnosed and treatment is started. A 60-year-old Caucasian male was admitted to our hospital with progressive melena. Gastroscopy and colonoscopy did not reveal the cause of the melena, but magnetic resonance imaging showed a jejunal tumor. After laparoscopic resection, the tumor appeared to be a grade 2 leiomyosarcoma. Small bowel neoplasms can be accurately detected by magnetic resonance enterography or wireless capsule endoscopy. Treatment almost always consists of resection of the primary tumor and its metastases. The role of chemo- and radiotherapy is not yet clear and prognosis remains very poor, with low five-year survival rates.
引用
收藏
页码:381 / 384
页数:4
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