Damron T A, Rahman D, Cashman M D
Department of Pathology, University of Illinois College of Medicine, Peoria.
Am J Gastroenterol. 1989 Sep;84(9):1109-14.
Gangliocytic paraganglioma is an extremely rare benign neurogenic tumor nearly exclusively located in the second portion of the duodenum, also the most common site of duodenal diverticula. A case is reported of a gangliocytic paraganglioma presenting in a 65-yr-old woman with a 1-yr history of postprandial cramping abdominal pain culminating in a single episode of melena leading to laparotomy. The tumor was identified with difficulty by endoscopy following negative barium studies. Histologically, the tumor is composed of carcinoid-like cells admixed with varying numbers of ganglion cells in a substratum of neuroid spindle cells. The epithelioid cells contain argyrophilic cytoplasmic granules confirmed by electron microscopy to be dense core membrane-bound secretory granules. Review of the literature suggests the tumor described is typical both clinically and pathologically of gangliocytic paraganglioma of the duodenum, except for its unprecedented occurrence in association with a duodenal diverticulum.
神经节细胞性副神经节瘤是一种极其罕见的良性神经源性肿瘤,几乎仅位于十二指肠第二部,而十二指肠第二部也是十二指肠憩室最常见的部位。本文报告了一例神经节细胞性副神经节瘤,患者为一名65岁女性,有1年餐后腹部绞痛病史,最终出现一次黑便,导致接受剖腹手术。钡餐检查结果为阴性,随后通过内镜检查才艰难地发现了肿瘤。组织学上,肿瘤由类癌样细胞与不同数量的神经节细胞混合组成,位于神经样梭形细胞基质中。上皮样细胞含有嗜银性胞质颗粒,电子显微镜证实这些颗粒为致密核心膜结合分泌颗粒。文献回顾表明,除了该肿瘤前所未有的与十二指肠憩室相关联的情况外,所描述的肿瘤在临床和病理上均为典型的十二指肠神经节细胞性副神经节瘤。