Suppr超能文献

浅表性CD34阳性纤维母细胞瘤的临床病理特征

Clinicopathological features of superficial CD34-positive fibroblastic tumor.

作者信息

Ding Li, Xu Wen-Jing, Tao Xiao-Ying, Zhang Liang, Cai Zhao-Gen

机构信息

Department of Pathology, The First Affiliated Hospital of Bengbu Medical College, Bengbu 233000, Anhui Province, China.

Department of Pathology, Hangzhou People's Hospital, Hangzhou 310000, Zhejiang Province, China.

出版信息

World J Clin Cases. 2021 Apr 26;9(12):2739-2750. doi: 10.12998/wjcc.v9.i12.2739.

Abstract

BACKGROUND

Superficial CD34-positive fibroblastoma (SCPFT) is a newly discovered mesenchymal tumor characterized by high polymorphism, low mitotic rate, and diffuse CD34-positive reactions.

AIM

To further determine the clinicopathological features of SCPFT.

METHODS

We retrospectively analyzed the clinicopathological data, immunohistochemistry results, and differential diagnoses of four patients with SCPFT and performed a literature review. Relevant fusion genes were also detected.

RESULTS

The tumors were all located in the lower extremities and presented as slow-growing painless masses located in the dermis and subcutaneous tissue. Microscopically, the tumors were composed of spindle-shaped to epithelioid cells with scattered abnormal and pleomorphic nuclei on a fibrous or fibromyxoid background. Necrosis was not found in the tumor tissues, and mitotic figures were rare. Immunohistochemically, the tumor cells were strongly positive for vimentin and CD34, and CKpan showed focal positivity in two tumors. All four patients were followed (13-57 mo, mean 35 mo), and one patient experienced local recurrence.

CONCLUSION

SCPFT is a newly discovered borderline mesenchymal tumor that can locally recur or even metastasize. Familiarity with its clinicopathological features will help avoid confusion with skin mesenchymal tumors with similar features.

摘要

背景

浅表性CD34阳性成纤维细胞瘤(SCPFT)是一种新发现的间叶性肿瘤,具有高度多形性、低有丝分裂率和弥漫性CD34阳性反应的特点。

目的

进一步明确SCPFT的临床病理特征。

方法

回顾性分析4例SCPFT患者的临床病理资料、免疫组化结果及鉴别诊断情况,并进行文献复习。同时检测相关融合基因。

结果

肿瘤均位于下肢,表现为生长缓慢的无痛性肿块,位于真皮和皮下组织。镜下,肿瘤由梭形至上皮样细胞组成,在纤维或纤维黏液样背景上可见散在的异常和多形性核。肿瘤组织中未发现坏死,有丝分裂象罕见。免疫组化显示,肿瘤细胞波形蛋白和CD34呈强阳性,细胞角蛋白广谱(CKpan)在2例肿瘤中呈局灶性阳性。4例患者均获随访(13 - 57个月,平均35个月),1例患者出现局部复发。

结论

SCPFT是一种新发现的交界性间叶性肿瘤,可局部复发甚至转移。熟悉其临床病理特征有助于避免与具有相似特征的皮肤间叶性肿瘤相混淆。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df4c/8058686/93768901d558/WJCC-9-2739-g001.jpg

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