Morita Tomoko, Tamura Satoru, Yokoyama Yuichi, Onishi Tomoko, Kuratani Yoshinori, Mizuta Hiroshi, Onishi Saburo
Department of Gastroenterology and Hepatology, Kochi Medical School, Kohasu, Kochi, Japan.
Dig Dis Sci. 2007 Jun;52(6):1400-4. doi: 10.1007/s10620-006-9370-3. Epub 2007 Apr 6.
A gangliocytic paraganglioma (GP) is an extremely rare neurogenic tumor nearly located in the second portion of the duodenum and has been regarded as benign. We report a case of duodenal GP in a 53-year-old man. The GP arose in the second portion of the duodenum and was shown by histological examination to consist of epithelioid cells, spindle cells, and ganglion-like cells. An endoscopic ultrasonography showed a round, well-demarcated, inhomogeneous, submucosal tumor in the 3rd-4th layer. We resected it by endoscopic mucosal resection.
神经节细胞性副神经节瘤(GP)是一种极其罕见的神经源性肿瘤,几乎都位于十二指肠第二部,一直被认为是良性的。我们报告一例53岁男性十二指肠GP病例。该GP发生于十二指肠第二部,组织学检查显示由上皮样细胞、梭形细胞和神经节样细胞组成。内镜超声显示在第3 - 4层有一个圆形、边界清晰、不均匀的黏膜下肿瘤。我们通过内镜黏膜切除术将其切除。