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下颌下淋巴结指状突树突状细胞肿瘤:病例报告及文献复习

Interdigitating Dendritic Cell Tumor of Submandibular Lymph Node: Case Report and Literature Review.

作者信息

Felezi Soroush, Nosrati Anahita, Eslami Jouybari Mohammad, Jafarshad Javane

机构信息

Department of Pathology, Imam Khomeini Hospital, Mazandaran University of Medical Sciences, Sari, Iran.

Gastrointestinal Cancer Research Center, Mazandaran University of Medical Sciences, Sari, Iran.

出版信息

Iran J Pathol. 2021 Spring;16(2):237-242. doi: 10.30699/IJP.2020.120698.2411. Epub 2020 Dec 21.

DOI:10.30699/IJP.2020.120698.2411
PMID:33936237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8085297/
Abstract

Dendritic cells (DCs) are key arms of immune system, which act in antigen presenting processes, and are considered as a bridge between innate and adaptive immune responses. DCs are found in both lymphoid and non-lymphoid organs. They are called interdigitating dendritic cells (IDCs) in secondary lymphoid organs. IDCs lack lineage surface markers and are positive for S-100 and vimentin. IDC sarcoma (IDCS) is a very rare neoplasm, which mainly affects lymph nodes, though there are reports of extra-nodal involvement. IDCS is thought to have poor prognosis. Although there is no consensus on the treatment modalities, such options as radical surgery, chemotherapy, and radiotherapy are performed depending on severity and site of the lesion. In this study, we present a case of IDCS in a 53-year-old male with a history of several skin lesions and prior diagnoses of basal cell carcinoma (BCC), squamous cell carcinoma (SCC), and metatypical carcinoma (MTC).

摘要

树突状细胞(DCs)是免疫系统的关键组成部分,在抗原呈递过程中发挥作用,被视为固有免疫和适应性免疫反应之间的桥梁。DCs存在于淋巴器官和非淋巴器官中。在次级淋巴器官中,它们被称为交错突树突状细胞(IDCs)。IDCs缺乏谱系表面标志物,S-100和波形蛋白呈阳性。IDCs肉瘤(IDCS)是一种非常罕见的肿瘤,主要累及淋巴结,不过也有结外受累的报道。IDCS的预后被认为较差。尽管在治疗方式上尚未达成共识,但根据病变的严重程度和部位,可采取根治性手术、化疗和放疗等治疗方案。在本研究中,我们报告了一例53岁男性的IDCS病例,该患者有多处皮肤病变病史,之前曾被诊断为基底细胞癌(BCC)、鳞状细胞癌(SCC)和化生型癌(MTC)。

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引用本文的文献

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本文引用的文献

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Interdigitating dendritic cell sarcoma of the spleen with hepatic failure after chemotherapy: A case report.化疗后脾脏指突状树突细胞肉瘤伴肝功能衰竭:一例报告
Medicine (Baltimore). 2019 May;98(19):e15535. doi: 10.1097/MD.0000000000015535.
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Genomic characterization of metastatic ultra-hypermutated interdigitating dendritic cell sarcoma through rapid research autopsy.通过快速研究尸检对转移性超高度突变的指状突树突状细胞肉瘤进行基因组特征分析。
Oncotarget. 2019 Jan 8;10(3):277-288. doi: 10.18632/oncotarget.26352.
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Interdigitating dendritic cell sarcoma located in the groin: a case report and literature review.腹股沟区指状突树突状细胞肉瘤1例报告并文献复习
J Int Med Res. 2018 Nov;46(11):4791-4799. doi: 10.1177/0300060518792444. Epub 2018 Sep 17.
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A case of interdigitating dendritic cell sarcoma studied by whole-exome sequencing.一例通过全外显子组测序研究的指突状树突细胞肉瘤
Genes Genomics. 2018 Dec;40(12):1279-1285. doi: 10.1007/s13258-018-0724-y. Epub 2018 Aug 11.
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Neoplastic PD-L1 expression on interdigitating dendritic cell sarcoma: A supplementary study of a case report.指状突树突状细胞肉瘤的肿瘤性程序性死亡配体1表达:一例病例报告的补充研究
Pathol Int. 2018 Oct;68(10):577-578. doi: 10.1111/pin.12711. Epub 2018 Aug 9.
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Interdigitating dendritic cell tumor: A rare case report with review of literature.交错突细胞肿瘤:1例罕见病例报告并文献复习
J Cancer Res Ther. 2018 Apr-Jun;14(3):690-693. doi: 10.4103/0973-1482.183189.
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