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微创干预后嗜酸性肉芽肿消退。病例报告及文献综述。

Resolution of eosinophilic granuloma after minimal intervention. Case report and review of literature.

作者信息

Chkoura Ahmed, El Alloussi Mustapha, Taleb Bouchra, El Wady Wafae

机构信息

Department of Oral Surgery, Faculty of Dentistry, University of Mohammed V, Rabat, Morocco.

出版信息

N Y State Dent J. 2010 Mar;76(2):43-6.

Abstract

Langerhans cell histiocytosis (LCH), previously known as histiocytosis X, is a rare, proliferative disorder in which the accumulation of pathologic Langerhans cells leads to local tissue infiltration and destruction. The incidence of LCH is estimated to be one case per 200,000 children per year. The role of the dentist is important in early and accurate evaluation, staging and diagnosis of LCH, because it may mimic more common diseases, such as juvenile periodontitis and osteomyelitis. There are multiple treatment options, but the response is unpredictable. The aim of this paper is to give a short, introductory overview on current diagnostic and treatment strategies for LCH in the oral and maxillofacial region and to present a case of LCH that mimicked juvenile periodontitis and was resolved following extraction of affected teeth. The history, radiological appearance, differential diagnosis, histopathology and treatment options for the patient are discussed.

摘要

朗格汉斯细胞组织细胞增多症(LCH),以前称为组织细胞增多症X,是一种罕见的增殖性疾病,其中病理性朗格汉斯细胞的积累导致局部组织浸润和破坏。据估计,LCH的发病率为每年每20万名儿童中有1例。牙医在LCH的早期准确评估、分期和诊断中起着重要作用,因为它可能模仿更常见的疾病,如青少年牙周炎和骨髓炎。有多种治疗选择,但反应不可预测。本文的目的是简要介绍口腔颌面部LCH的当前诊断和治疗策略,并介绍一例模仿青少年牙周炎且在拔除患牙后得到解决的LCH病例。讨论了该患者的病史、影像学表现、鉴别诊断、组织病理学和治疗选择。

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