首页> 外文期刊>Journal of Clinical and Diagnostic Research >Multiple Primary Dedifferentiated Liposarcoma of the Jejunal Mesentery:A Case Report and Review of Literature
【24h】

Multiple Primary Dedifferentiated Liposarcoma of the Jejunal Mesentery:A Case Report and Review of Literature

机译:空肠系膜多原发性去分化性肉瘤:一例病例报告并文献复习

获取原文
获取外文期刊封面目录资料

摘要

Liposarcoma arising primarily from the intestinal mesentery is a rare malignancy. Malignancy is said to be synchronous when there is occurrence of two or more tumours that have not spread from a common site or recurred and show no evidence of metastasis. Multiple synchronous primary liposarcoma of the mesentery is a very unusual clinical finding. Here, we report a rare case of synchronous multiple primary dedifferentiated liposarcoma of jejunal mesentery in a 36-year-old female patient. Radiological investigations aided in making a provisional diagnosis of an ovarian malignancy. A staging laparotomy was performed and general surgeon?s help was sought due to the presence of three separate jejunal mesenteric masses of sizes 8x6 cms, 6x6 cms and 25x20 cms respectively. Complete excision of mesenteric masses with one feet of involved jejunum was done and a jejuno-jejunal anastomosis made. The histopathology report was indicative of multiple dedifferentiated liposarcoma of jejunal mesentery. Postoperatively patient received Doxorubicin, Dacarbazine and Ifosfamide based adjuvant chemotherapy in view of poorly differentiated tumour. Patient remains tumour free for the last 12 months of follow up.
机译:主要由肠系膜引起的脂肪肉瘤是一种罕见的恶性肿瘤。当发生两个或两个以上尚未从同一部位扩散或复发且无转移迹象的肿瘤时,恶性肿瘤被认为是同步的。肠系膜的多个同步原发性脂肪肉瘤是非常不寻常的临床发现。在这里,我们报道了一名36岁女性患者发生的空肠系膜同步多发性原发性去分化脂肪肉瘤的罕见病例。放射学检查有助于对卵巢恶性肿瘤进行临时诊断。由于存在三个分别为8x6 cms,6x6 cms和25x20 cms大小的空肠肠系膜肿块,因此进行了分期剖腹手术并寻求全科医生的帮助。用一只脚的空肠完全切除肠系膜肿块,并进行空肠-空肠吻合术。组织病理学报告表明空肠系膜多发性去分化脂肪肉瘤。鉴于肿瘤分化程度低,术后患者接受了阿霉素,达卡巴嗪和异环磷酰胺辅助化疗。在随访的最后12个月中,患者无肿瘤。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号