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An affordable immunohistochemical approach to estimate the prevalence of in large cohort studies-establishing the baseline rate of mutation in an institutional series of papillary thyroid carcinoma from Thailand.一种经济实惠的免疫组织化学方法,用于在大型队列研究中估计[具体内容缺失]的患病率——确定泰国某机构一系列甲状腺乳头状癌中[具体内容缺失]突变的基线率。
Gland Surg. 2020 Oct;9(5):1867-1877. doi: 10.21037/gs-20-388.
2
VE1 Immunohistochemistry Improves the Limit of Genotyping for Detecting Mutation in Papillary Thyroid Cancer.VE1免疫组化提高了甲状腺乳头状癌中检测突变的基因分型限度。
Cancers (Basel). 2020 Mar 5;12(3):596. doi: 10.3390/cancers12030596.
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Teaching NeuroImages: CNS pituitary-hypothalamic Langerhans cell histiocytosis in an adult.
Neurology. 2020 Jan 28;94(4):e434-e435. doi: 10.1212/WNL.0000000000008850. Epub 2020 Jan 13.
4
BRAF gene mutations in synchronous papillary thyroid carcinoma and Langerhans cell histiocytosis co-existing in the thyroid gland: a case report and literature review.甲状腺内共存的同步乳头状甲状腺癌和朗格汉斯细胞组织细胞增生症中的 BRAF 基因突变:病例报告及文献复习。
BMC Cancer. 2019 Feb 22;19(1):170. doi: 10.1186/s12885-019-5372-3.
5
Langerhans cell histiocytosis in adults: Advances in pathophysiology and treatment.成人朗格汉斯细胞组织细胞增生症:病理生理学和治疗进展。
Cancer Sci. 2018 Dec;109(12):3707-3713. doi: 10.1111/cas.13817. Epub 2018 Oct 30.
6
Langerhans-Cell Histiocytosis.朗格汉斯细胞组织细胞增多症
N Engl J Med. 2018 Aug 30;379(9):856-868. doi: 10.1056/NEJMra1607548.
7
Successful management of multiple-systemic Langerhans cell histiocytosis involving endocrine organs in an adult: A case report and review of literature.成人多系统朗格汉斯细胞组织细胞增多症累及内分泌器官的成功管理:一例报告并文献复习
Medicine (Baltimore). 2018 Jun;97(26):e11215. doi: 10.1097/MD.0000000000011215.
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Langerhans cell histiocytosis and primary hemophagocytic lymphohistiocytosis with persistent clonal T-large granular lymphocyte proliferation.
Ann Hematol. 2018 Jul;97(7):1295-1296. doi: 10.1007/s00277-018-3298-5. Epub 2018 Mar 26.
9
and Langerhans Cell Histiocytosis.以及朗格汉斯细胞组织细胞增多症。
Iran J Pathol. 2017 Fall;12(4):323-328. Epub 2017 Nov 1.
10
Clinicopathological and Immunohistochemical Study of Head and Neck Langerhans Cell Histiocytosis from Latin America.拉丁美洲头颈部朗格汉斯细胞组织细胞增多症的临床病理及免疫组织化学研究
Head Neck Pathol. 2018 Dec;12(4):431-439. doi: 10.1007/s12105-017-0867-1. Epub 2017 Nov 21.

甲状腺朗格汉斯细胞组织细胞增生症与 Epstein-Barr 病毒相关。

Epstein-Barr Virus-Associated Langerhans Cell Histiocytosis of the Thyroid Gland.

机构信息

Department of Pathology, Kameda Medical Center, 929 Higashi-cho, Kamogawa, Chiba, 296-8602, Japan.

Department of Otorhinolaryngology, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand.

出版信息

Head Neck Pathol. 2021 Sep;15(3):1054-1058. doi: 10.1007/s12105-020-01247-8. Epub 2020 Nov 2.

DOI:10.1007/s12105-020-01247-8
PMID:33140265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8385082/
Abstract

Thyroid gland involvement of Langerhans cell histiocytosis (LCH) is extremely rare in both systemic and isolated disease. The role of viral infection in LCH development is not yet fully understood. Although several viruses are proposed as etiologic factors, such as Epstein-Barr virus (EBV) and human herpesvirus 6 (HHV-6), they seem to play a bystander role in LCH. A 29-year old female patient with a prior history of multisystemic LCH (pituitary gland and skull bone), presented with a thyroid nodule. The patient underwent a total thyroidectomy and the histological examination revealed nodular lesions composed of sheets and clusters of histiocytes in the inflammatory background. The histiocytes stained positive for S-100 and CD1a and were negative for HHV-8, cytomegalovirus, and VE1 (anti-BRAF) on immunohistochemistry. The EBER in situ hybridization for EBV showed frequent positive-stained cells. The conventional PCR analysis for EBV was positive and qPCR analysis confirmed a significant DNA copy number difference (p = 0.02) between the tumor and adjacent non-neoplastic thyroid tissue. PCR analysis for HHV-6, HPV, HSV was negative in both tumor and benign samples. In conclusion, the presented case showed a rare thyroid involvement by LCH associated with EBV infection, which has not been reported before. Further studies are required to investigate a possible etiologic link between EBV infection and LCH.

摘要

朗格汉斯细胞组织细胞增生症(LCH)累及甲状腺极为罕见,无论是在系统性疾病还是孤立性疾病中。病毒感染在 LCH 发病机制中的作用尚未完全阐明。尽管有几种病毒被认为是病因因素,如 EBV 和 HHV-6,但它们似乎在 LCH 中起旁观者作用。一位 29 岁女性患者既往有多系统 LCH(垂体和颅骨)病史,现出现甲状腺结节。患者接受了全甲状腺切除术,组织学检查显示在炎症背景下存在由组织细胞片状和簇状组成的结节性病变。组织细胞免疫组织化学染色 S-100 和 CD1a 阳性,HHV-8、巨细胞病毒和 VE1(抗 BRAF)阴性。EBV 的 EBER 原位杂交显示频繁的阳性染色细胞。常规 EBV PCR 分析为阳性,qPCR 分析证实肿瘤和相邻非肿瘤性甲状腺组织之间存在显著的 DNA 拷贝数差异(p=0.02)。肿瘤和良性样本的 HHV-6、HPV、HSV 的 PCR 分析均为阴性。总之,本例罕见的 LCH 累及甲状腺与 EBV 感染相关,此前尚未有报道。需要进一步研究以探讨 EBV 感染与 LCH 之间可能存在的病因联系。