Li Jiannan, Le Hanxiang, Chai Wei, Zhou Yan, Jin Lifang, Liu Tongjun, Zhang Kai
Department of General Surgery, The Second Hospital of Jilin University Department of Gynecology and Obstetrics, The First Hospital of Jilin University Department of Hematology and Oncology, The Second Hospital of Jilin University, Changchun, Jilin, China.
Medicine (Baltimore). 2017 Aug;96(31):e7684. doi: 10.1097/MD.0000000000007684.
Intraabdominal fibromatosis is a rare benign tumor that often affects the mesentery or retroperitoneum, and can infiltrate adjacent organs. However, it is rare for fibromatosis to arise from the small intestinal wall.
A 27-year-old female with a tangible abdominal tumor is described.
The computed tomography (CT) scan revealed a 7.5 cm, small intestine-associated tumor in the right abdomen.
The patient received tumor resection and intestinal anastomosis.
Further pathological examination confirmed the tumor as a duodenal fibromatosis that infiltrated the intestinal wall. To the best of our knowledge, this is the first report of a duodenum-derived fibromatosis that invaded the muscular layer of the intestine.
Our study demonstrated that an unexplained abdominal mass should be noteworthy and properly treated.
腹腔纤维瘤病是一种罕见的良性肿瘤，常累及肠系膜或腹膜后，可浸润相邻器官。然而，纤维瘤病起源于小肠壁的情况较为罕见。
描述了一名27岁有腹部可触及肿物的女性。
计算机断层扫描（CT）显示右腹部有一个7.5厘米与小肠相关的肿瘤。
患者接受了肿瘤切除及肠吻合术。
进一步病理检查证实肿瘤为浸润肠壁的十二指肠纤维瘤病。据我们所知，这是首例起源于十二指肠并侵犯肠肌层的纤维瘤病报告。
我们的研究表明，不明原因的腹部肿块应引起重视并得到妥善治疗。
