消化道颗粒细胞瘤九例分析及文献复习
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  • 英文篇名:An analysis on clinical and pathologic features of 9 cases with granular cell tumors in digestive tract and review of literatures
  • 作者:张淑红 ; 岳冰 ; 于海云 ; 郑媛媛 ; 柳玮华
  • 英文作者:ZHANG Shu-hong;YUE Bing;YU Hai-yun;Department of Pathology,Beijing Friendship Hospital,Capital Medical University;Department of Pathology,Capital Medical University Electric Power Teaching Hospital;
  • 关键词:消化道 ; 颗粒细胞瘤 ; 临床病理 ; 免疫组织化学
  • 英文关键词:Digestive tract;;Granular cell tumor;;Clinical pathology;;Immunohistochemistry
  • 中文刊名:SYLC
  • 英文刊名:Journal of Clinical and Experimental Medicine
  • 机构:首都医科大学附属北京友谊医院病理科;首都医科大学电力教学医院病理科;
  • 出版日期:2018-06-10
  • 出版单位:临床和实验医学杂志
  • 年:2018
  • 期:v.17;No.267
  • 语种:中文;
  • 页:SYLC201811033
  • 页数:3
  • CN:11
  • ISSN:11-4749/R
  • 分类号:115-117
摘要
目的探讨消化道颗粒细胞瘤的临床病理学特点、鉴别诊断、治疗及预后。方法收集并回顾性分析北京友谊医院2009年至2016年间诊断的9例消化道颗粒细胞瘤的临床特点、组织形态学及免疫表型特点,并复习相关文献。结果研究共纳入9例患者,其中男性5例,女性4例;年龄39~67岁,平均年龄52±9岁。肿物直径0.2~1.2cm,平均直径0.56±0.28 cm。9例患者治疗均采用内镜下黏膜切除术。显微镜下肿瘤呈浸润性生长,瘤细胞排列成巢状或片状,胞质丰富、嗜酸性,核小位于细胞中央。未见坏死及核分裂。免疫组化肿瘤细胞表达S-100、CD68、Vimentin。结论消化道颗粒细胞瘤是一种少见的神经源性肿瘤,主要发生在食管,少见发生在胃及结肠。确诊需要依靠病理形态学及免疫组织化学。推荐的治疗方法是内镜下黏膜切除术。
        Objective To explore the clinicopathological features,differential diagnosis and treatment of granular cell tumor in digestive tract. Methods Nine cases of granular cell tumor in digestive tract diagnosed in this hospital during 2009 to 2016 were collected for this study.The clinical characteristics,pathological features and immunological expressioin were analyzed,and their morphological features were studied by gross examination,light microscopy and immunohistochemical exaination,and accompanied with review of related literatures. Results Five cases were males and four females,the average age of these patients was 52 ± 9 years old( with age range of 39 to 67 years old). The size of tumors ranged from 0. 2 to 1. 2 cm in greatest dimension,and their average diameter was 0. 56 ± 0. 28 cm. All these patients received endoscopic mucosal endoscopical resection,the growth pattern was nested or solid with infiltrative margin,tumor cells had abundant eosinophilic cytoplasm with a small central nucleus,mitosis and necrosis were absent in all cases. Immunohistochemically,all cases showed positive for S-100,CD68 and Vimentin expression. Conclusion Granular cell tumor in digestive tract is a rare neoplasm of neural derivation,most commonly occur in esophageal,rarely occur in stomach and colon. Its dignosis depends on pathomorphological examination and immunophenotyping. Endoscopic mucosal resection is recommended as a therapeutic method.
引文
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