• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

显示神经分化的结肠系膜黏液样错构瘤:超微结构和免疫组织化学研究

Mesocolic myxoid hamartoma showing neural differentiation: an ultrastructural and immunohistochemical study.

作者信息

Henriquez A, Latorre J J, Gonzalez S

机构信息

Department of Pediatric Pathology, Hospital Luis Calvo Mackenna, Santiago de Chile.

出版信息

Pediatr Pathol. 1989;9(5):559-66. doi: 10.3109/15513818909026914.

DOI:10.3109/15513818909026914
PMID:2813202
Abstract

A myxoid mesocolic tumor in a 4-month-old female infant is described. The tumor weighed 190 g and measured 8 cm in diameter and presented as a single mass composed of stellate and round cells with vesicular nuclei and prominent nucleoli in a myxoid, well-vascularized stroma. Electron microscopy showed mesenchymal cells with dilated rough endoplasmic reticulum, cell projections with primitive and desmosome-like cell junctions, and basal membrane-like material. Immunohistochemical studies demonstrated immunoreactivity with antibodies against vimentin and S-100 protein. The infant is well and without evidence of disease 3 years after surgery. This is an example of a peripheral myxoid hamartoma with neural differentiation, and the tumor is expected to have a benign clinical course.

摘要

本文描述了一名4个月大女婴的黏液样结肠系膜肿瘤。该肿瘤重190克,直径8厘米,表现为单个肿块,由星状和圆形细胞组成,细胞核呈泡状,核仁明显,位于黏液样、血管丰富的间质中。电子显微镜显示间充质细胞的粗面内质网扩张,细胞突起有原始的和桥粒样细胞连接,以及基底膜样物质。免疫组织化学研究表明,该肿瘤对波形蛋白和S-100蛋白抗体呈免疫反应性。术后3年,该婴儿情况良好,无疾病迹象。这是一例具有神经分化的外周黏液样错构瘤,预计该肿瘤临床病程为良性。

相似文献

1
Mesocolic myxoid hamartoma showing neural differentiation: an ultrastructural and immunohistochemical study.显示神经分化的结肠系膜黏液样错构瘤:超微结构和免疫组织化学研究
Pediatr Pathol. 1989;9(5):559-66. doi: 10.3109/15513818909026914.
2
Gastrointestinal stromal tumors with prominent myxoid matrix. Clinicopathologic, immunohistochemical, and ultrastructural study of nine cases of a distinctive morphologic variant of myogenic stromal tumor.伴有显著黏液样基质的胃肠道间质瘤。9例肌源性间质瘤独特形态学变异型的临床病理、免疫组化及超微结构研究
Am J Surg Pathol. 1995 Jan;19(1):59-70.
3
Immunohistochemical and electron microscopic findings in a case of mixed hamartoma of the liver.肝混合性错构瘤一例的免疫组化及电镜检查结果
Jpn J Surg. 1990 Jan;20(1):101-6. doi: 10.1007/BF02470721.
4
Extraskeletal myxoid chondrosarcoma: a light microscopic, immunohistochemical, ultrastructural and immuno-ultrastructural study indicating neuroendocrine differentiation.骨外黏液样软骨肉瘤:一项光镜、免疫组化、超微结构及免疫超微结构研究表明其具有神经内分泌分化。
Histopathology. 2001 Nov;39(5):514-24. doi: 10.1046/j.1365-2559.2001.01277.x.
5
Mesenchymal hamartoma of the liver: A proliferative lesion of possible hepatic stellate cell (Ito cell) origin.肝脏间叶性错构瘤:一种可能源于肝星状细胞(Ito 细胞)的增生性病变。
Pathol Res Pract. 2010 Jul 15;206(7):532-6. doi: 10.1016/j.prp.2010.02.009.
6
Fibrous hamartoma of infancy: an ultrastructural study.婴儿纤维性错构瘤:超微结构研究
Hum Pathol. 1984 Aug;15(8):717-23. doi: 10.1016/s0046-8177(84)80161-6.
7
Omental-mesenteric myxoid hamartomas. Infantile lesions simulating malignant tumors.网膜-肠系膜黏液样错构瘤。模拟恶性肿瘤的婴儿期病变。
Am J Surg Pathol. 1983 Sep;7(6):567-78. doi: 10.1097/00000478-198309000-00007.
8
Fibrous hamartoma of infancy: an immunohistochemical and ultrastructural study.婴儿纤维性错构瘤:一项免疫组织化学和超微结构研究
Hum Pathol. 1991 Sep;22(9):914-8. doi: 10.1016/0046-8177(91)90182-o.
9
Fibrous hamartoma of the tongue: report of a case with immunohistochemical and ultrastructural studies.舌部纤维性错构瘤:一例免疫组织化学及超微结构研究报告
Int J Pediatr Otorhinolaryngol. 1995 Oct;33(2):171-8. doi: 10.1016/0165-5876(95)01206-q.
10
Ovarian myxoma: ultrastructural and immunohistochemical findings.卵巢黏液瘤:超微结构及免疫组化研究结果
Ultrastruct Pathol. 1992 Jul-Aug;16(4):429-38. doi: 10.3109/01913129209057828.

引用本文的文献

1
Infantile inflammatory myofibroblastic tumors: clinicopathological and molecular characterization of 12 cases.婴儿炎性肌纤维母细胞瘤 12 例临床病理及分子特征分析
Mod Pathol. 2020 Apr;33(4):576-590. doi: 10.1038/s41379-019-0406-6. Epub 2019 Nov 5.
2
Primary omental-mesenteric myxoid hamartoma of the mesoappendix incidentally detected after abdominal trauma in a child: report of a case.
Surg Today. 2005;35(9):792-5. doi: 10.1007/s00595-005-3006-7.