Kawaguchi K, Takizawa T, Koike M, Tabata I, Goseki N
Virchows Arch A Pathol Anat Histopathol. 1985;406(3):373-80. doi: 10.1007/BF00704306.
We report multiple paraganglioneuromas which occurred in a 40-year-old-man. Thirty-two tumours with similar histological appearance have been reported previously and most of them showed a striking predilection to occur in the second portion of the duodenum. In this case, three masses were detected; one was located in the periampullary region of duodenum with a polypoid appearance, the others were well defined masses in peri-pancreatic tissue adjacent to large vessels. Histology revealed two cellular components, epithelioid cells with NSE immunoreactivity and S-100 protein containing spindle-shaped cells. Moreover, on electron microscopical examination, three different epithelioid cell types were seen. Type I was a figure differentiating to ganglion cells, type II to paraganglion cells, type III was a hybrid form of ganglion and paraganglion cells. Paraganglioneuroma revealed the histopathology of ganglioneuroma, paraganglioma and also a mixed appearance. In this respect the tumour may be considered to originate in undifferentiated neural crest cells and develop organoid differentiation.
我们报告了一名40岁男性身上发生的多发性副神经节瘤。此前已有32例具有相似组织学表现的肿瘤报道,其中大多数显著倾向于发生在十二指肠第二部。在该病例中,检测到三个肿块;一个位于十二指肠壶腹周围区域,呈息肉样外观,其他两个是在与大血管相邻的胰腺周围组织中边界清晰的肿块。组织学显示有两种细胞成分,具有NSE免疫反应性的上皮样细胞和含有S - 100蛋白的梭形细胞。此外,电子显微镜检查可见三种不同类型的上皮样细胞。I型是向神经节细胞分化的形态,II型向副神经节细胞分化,III型是神经节细胞和副神经节细胞的混合形式。副神经节瘤显示出神经节瘤、副神经节瘤的组织病理学特征,还有混合外观。在这方面,该肿瘤可被认为起源于未分化的神经嵴细胞并发展为类器官分化。