Suppr超能文献

手术作为颌骨嗜酸性肉芽肿唯一治疗方法的疗效

Outcome of Surgery as Sole Treatment of Eosinophilic Granuloma of Jaws.

作者信息

Nezafati Saeed, Yazdani Javad, Shahi Shahriar, Mehryari Mahsa, Hajmohammadi Emran

机构信息

Dept. of Oral & Maxillofacial Surgery, School of Dentistry, Tabriz University of Medical Sciences, Tabriz, Iran.

Dept. of Oral and Maxillofacial Surgery, School of Dentistry, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

J Dent (Shiraz). 2019 Sep;20(3):210-214. doi: 10.30476/DENTJODS.2019.44903.

Abstract

Langerhans cell histiocytosis (LCH) is characterized by the congregation of proliferating langerhans cells (LC). Langerhans cells are a part of dendritic cell system of primary immune response that is responsible for presenting antigen to lymphocytes. Being a rare disease, the total incidence of LCH is reported to be 1 in 2 million people. LCH mainly affects children and young adults, with a slight male predilection. LCH is clinically divided into three groups namely Letter-Siwe disease (multiple multi organ affecting LCH at very young age), Hand-Schuler-Christian disease (LCH of bone involvement exophthalmos and diabetes insipidus), and Eosinophilic granuloma (LCH of bone, solitary or multiple). The extent of involvement influences the treatment planning. In this retrospective study, we survey five patients with eosinophilic granuloma in jaws (bony LCH). The diagnosis was confirmed by tissue biopsy and histopathologic examination. Surgery and curettage of the lesions were carried out under general or local anesthesia. After surgery, the patients were examined clinically every 6 month in the first year and then once in a year. The overall outcome was excellent. According to the results, it can be concluded that surgical curettage of localized eosinophilic granuloma is an appropriate and sufficient treatment.

摘要

朗格汉斯细胞组织细胞增多症(LCH)的特征是增殖的朗格汉斯细胞(LC)聚集。朗格汉斯细胞是初级免疫反应中树突状细胞系统的一部分,负责将抗原呈递给淋巴细胞。作为一种罕见疾病,据报道LCH的总发病率为百万分之一。LCH主要影响儿童和年轻人,男性略多。LCH临床上分为三组,即勒-雪病(极幼年时累及多个多器官的LCH)、汉-许-克病(累及骨骼、突眼和尿崩症的LCH)和嗜酸性肉芽肿(骨骼的LCH,单发或多发)。受累程度影响治疗方案的制定。在这项回顾性研究中,我们调查了5例颌骨嗜酸性肉芽肿(骨LCH)患者。诊断通过组织活检和组织病理学检查得以证实。在全身或局部麻醉下对病变进行手术刮除。术后,患者在第一年每6个月进行一次临床检查,之后每年检查一次。总体结果良好。根据结果可以得出结论,局部嗜酸性肉芽肿的手术刮除是一种合适且充分的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d88a/6732173/4039a9285c93/JDS-20-210-g002.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验