首页 > 期刊杂志 > 正文

Duodenal Gangliocytic Paraganglioma With Lymph Node Metastasis.

伴淋巴结转移的十二指肠节细胞副节瘤

Abstract

Gangliocytic paraganglioma is a rare tumor that occurs most commonly in the second portion of the duodenum. It is characterized by its triphasic cellular differentiation: epithelioid neuroendocrine cells, spindle cells with Schwann cell differentiation, and ganglion cells. Most gangliocytic paragangliomas are considered benign and are amenable to local excision. However, to our knowledge, 23 cases with lymph node metastasis have been reported, 1 case of bone metastasis, and 2 cases of liver metastases. Predictive factors that have been suggested for lymph node metastasis include size (larger than 2 cm), young age, and tumors exceeding the submucosal layer. Our objective was to review the clinical features, the histopathologic characteristics, and the differential diagnosis of gangliocytic paraganglioma and to discuss the value of the predictive factors for lymph node metastasis.

摘要

   节细胞副节瘤是一种罕见的肿瘤,常发生于十二指肠降段,其细胞具有三相分化的特点:上皮样神经内分泌细胞、伴雪旺氏细胞分化特征的梭形细胞和节细胞。大部分节细胞副节瘤是良性的,局部切除即可,然而据我们所知,已报道23例伴淋巴结转移的节细胞副节瘤,1例发生骨转移,2例发生肝转移。已表明,节细胞副节瘤预后因素与淋巴结转移、肿瘤大小(大于2cm)、年龄较轻和肿瘤浸润至粘膜下层有关。本文旨在讨论节细胞副节瘤的临床特点、组织病理学特征和鉴别诊断,探讨伴淋巴结转移的节细胞副节瘤的预后因素。


full text

我要评论

0条评论