An Unusual Case of Duodenal Neuroendocrine Tumor

被引:0
作者
Lu, Chun-Jing [1 ]
Xu, Zhong [2 ]
Huang, Wei-Feng [2 ,3 ]
机构
[1] Xiamen Univ, Women & Childrens Hosp, Sch Med, Dept Blood Transfus, Xiamen 361003, Peoples R China
[2] Xiamen Univ, Affiliated Hosp 1, Sch Med, Dept Gastroenterol & Hepatol, Xiamen 361003, Peoples R China
[3] Fujian Med Univ, Sch Clin Med, Fuzhou 350004, Peoples R China
关键词
Neuroendocrine tumor; Duodenum; Gastrointestinal bleeding; MANAGEMENT;
D O I
10.1007/s12262-024-04213-8
中图分类号
R61 [外科手术学];
学科分类号
摘要
A 68-year-old female presented with a 5-day history of melena. The patient had a prolonged history of irregular aspirin use. Physical examination revealed pallor of the skin and mucous membranes, with the absence of abdominal tenderness. Laboratory investigations showed normocytic anemia (70.0 g/L) and positive fecal occult blood. Liver function, kidney function, and tumor markers were within normal ranges. Esophagogastroduodenoscopy revealed a submucosal lesion in the duodenal bulb, measuring approximately 2 cm x 2 cm and resembling a "doughnut," with central ulceration and surrounding mucosal vascular dilation. Biopsy histopathology confirmed a G2-grade neuroendocrine tumor. Abdominal contrast-enhanced CT indicated thickening of the duodenal bulb wall with slight enlargement of surrounding lymph nodes. Subsequently, the patient underwent a distal gastrectomy with resection of the duodenal bulb. Postoperative pathology revealed the absence of vascular invasion and lymph node infiltration. Follow-up examinations, including gastric endoscopy and abdominal CT, revealed no signs of recurrence.
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页数:3
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