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本文引用的文献

1
Langerhans cell histiocytosis in children: History, classification, pathobiology, clinical manifestations, and prognosis.儿童朗格汉斯细胞组织细胞增生症:历史、分类、病理生物学、临床表现和预后。
J Am Acad Dermatol. 2018 Jun;78(6):1035-1044. doi: 10.1016/j.jaad.2017.05.059.
2
[Langerhans cell histiocytosis in adults].[成人朗格汉斯细胞组织细胞增多症]
Rev Med Interne. 2015 Oct;36(10):658-67. doi: 10.1016/j.revmed.2015.04.015. Epub 2015 Jul 3.
3
Langerhans cell histiocytosis with oral manifestations: a rare and unusual case report.伴有口腔表现的朗格汉斯细胞组织细胞增多症:一例罕见且特殊的病例报告
J Clin Exp Dent. 2012 Oct 1;4(4):e252-5. doi: 10.4317/jced.50728. eCollection 2012 Oct.
4
Therapy prolongation improves outcome in multisystem Langerhans cell histiocytosis.治疗时间的延长可改善多系统朗格汉斯细胞组织细胞增生症的预后。
Blood. 2013 Jun 20;121(25):5006-14. doi: 10.1182/blood-2012-09-455774. Epub 2013 Apr 15.
5
Langerhans cell histiocytosis: literature review and descriptive analysis of oral manifestations.朗格汉斯细胞组织细胞增多症:文献综述及口腔表现的描述性分析
Med Oral Patol Oral Cir Bucal. 2009 May 1;14(5):E222-8.
6
Langerhans cell histiocytosis: current insights in a molecular age with emphasis on clinical oral and maxillofacial pathology practice.朗格汉斯细胞组织细胞增多症:分子时代的最新见解,重点关注临床口腔颌面病理学实践
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005 Aug;100(2 Suppl):S42-66. doi: 10.1016/j.tripleo.2005.06.016.
7
Langerin (CD207) staining in normal pediatric tissues, reactive lymph nodes, and childhood histiocytic disorders.正常儿科组织、反应性淋巴结及儿童组织细胞疾病中的朗格汉斯蛋白(CD207)染色
Pediatr Dev Pathol. 2004 Nov-Dec;7(6):607-14. doi: 10.1007/s10024-004-3027-z. Epub 2004 Nov 8.
8
[Involvement of the maxillary sinus in Langerhans cell histiocytosis].[朗格汉斯细胞组织细胞增多症中上颌窦的累及情况]
Mund Kiefer Gesichtschir. 2003 Jan;7(1):36-41. doi: 10.1007/s10006-002-0433-0. Epub 2002 Oct 12.
9
Langerhans' cell histiocytosis in patients older than 21 years.21岁以上患者的朗格汉斯细胞组织细胞增多症。
Clin Orthop Relat Res. 2000 Oct(379):231-5. doi: 10.1097/00003086-200010000-00027.
10
Langerin, a novel C-type lectin specific to Langerhans cells, is an endocytic receptor that induces the formation of Birbeck granules.朗格素,一种对朗格汉斯细胞具有特异性的新型C型凝集素,是一种诱导伯贝克颗粒形成的内吞受体。
Immunity. 2000 Jan;12(1):71-81. doi: 10.1016/s1074-7613(00)80160-0.

鼻及上颌骨朗格汉斯细胞组织细胞增多症:一种罕见的表现

Langerhans Cell Histiocytosis of the Nose and Maxilla: A Rare Presentation.

作者信息

Sekar Raghul, Raja Kalaiarasi

机构信息

Department of Otorhinolaryngology , Saveetha Medical College and Hospital , Chennai, India.

Department of Otorhinolaryngology, Jawaharlal Institute of Postgraduate Medical Education and Research(JIPMER), Puducherry, 605006 India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2023 Dec;75(4):4106-4109. doi: 10.1007/s12070-023-04075-8. Epub 2023 Jul 23.

DOI:10.1007/s12070-023-04075-8
PMID:37974832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10646049/
Abstract

Langerhans cell histiocytosis (LCH) is a disease characterized by localized and generalized proliferation of the histiocytes. It is a locally aggressive condition. The clinical presentation is highly variable and can range from isolated, self-healing skin or bone lesions to life-threatening multisystem disease. It can present as a unifocal or multifocal disease. The majority are present in the head and neck region, but the involvement of Paranasal sinuses is rare. Here we describe a 64-years-old female who presented with a slow-growing left nasal mass for 1 year. Evaluation of the patient was suggestive of malignancy, but the biopsy report turned out to be Langerhans cell histiocytosis; subsequently left, total maxillectomy was done. We hereby present a unique case of LCH with isolated nose and paranasal sinus involvement.

摘要

朗格汉斯细胞组织细胞增多症(LCH)是一种以组织细胞局部和全身性增殖为特征的疾病。它是一种局部侵袭性疾病。临床表现高度多变,范围从孤立的、可自愈的皮肤或骨病变到危及生命的多系统疾病。它可表现为单灶性或多灶性疾病。大多数病例出现在头颈部区域,但鼻窦受累罕见。在此,我们描述一名64岁女性,她出现左侧鼻腔肿物缓慢生长1年。对该患者的评估提示为恶性,但活检报告结果为朗格汉斯细胞组织细胞增多症;随后进行了左侧全上颌骨切除术。我们在此呈现一例朗格汉斯细胞组织细胞增多症累及孤立鼻腔和鼻窦的独特病例。