• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

相似文献

1
Hand schuller christian disease: a rare case report with oral manifestation.汉-许-克病：一例伴有口腔表现的罕见病例报告
J Clin Diagn Res. 2015 Jan;9(1):ZD28-30. doi: 10.7860/JCDR/2015/10985.5481. Epub 2015 Jan 1.
2
Multidisciplinary approach in a case of Hand-Schüller-Christian disease with maxillary involvement.上颌骨受累的汉-许-克病病例的多学科治疗方法
Spec Care Dentist. 2018 Mar;38(2):107-111. doi: 10.1111/scd.12273. Epub 2018 Feb 8.
3
Aural symptoms as primary presentation of Langerhan's cell histiocytosis.以耳部症状为主要表现的朗格汉斯细胞组织细胞增多症。
Clin Otolaryngol Allied Sci. 1993 Aug;18(4):317-23. doi: 10.1111/j.1365-2273.1993.tb00856.x.
4
Oral mucosal lesions with transient self-healing of Langerhans cell histiocytosis: a case report.朗格汉斯细胞组织细胞增生症的口腔黏膜病变伴短暂自限性：病例报告。
Hua Xi Kou Qiang Yi Xue Za Zhi. 2023 Oct 1;41(5):592-598. doi: 10.7518/hxkq.2023.2023084.
5
A rare occurrence of Langerhans cell histiocytosis in an adult.成人罕见的朗格汉斯细胞组织细胞增多症病例。
J Oral Maxillofac Pathol. 2014 Sep-Dec;18(3):415-9. doi: 10.4103/0973-029X.151335.
6
A case report of langerhans histiocytosis presenting sequentially over a 21-year period with Letterer-Siwe disease, hand-Schuller-Christian disease and eosinophillic granuloma of bone.1例朗格汉斯细胞组织细胞增多症的病例报告，该病例在21年期间依次出现勒-雪病、汉-许-克病和骨嗜酸性肉芽肿。
J Pediatr Hematol Oncol. 2006 Nov;28(11):746-9. doi: 10.1097/01.mph.0000243650.51487.ff.
7
Electron microscopic study of the orbital lesion of Hand-Schüller-Christian disease.汉-许-克病眼眶病变的电子显微镜研究
J Pediatr Ophthalmol. 1977 Jul-Aug;14(4):242-7.
8
[Histiocytosis X. 3 different cases: eosinophilic granuloma, Hand-Schueller-Christian disease, Abt-Letterer-Siwe disease].[组织细胞增多症X。3种不同病例：嗜酸性肉芽肿、汉-许-克病、勒-雪病]
Ann Osp Maria Vittoria Torino. 1985 Jan-Jun;28(1-6):56-78.
9
Langerhans' Cell Histiocytosis Diagnosed through Periodontal Lesion in a 15-year-old Child: A Case Report.通过一名15岁儿童牙周病变诊断的朗格汉斯细胞组织细胞增多症：病例报告
Int J Clin Pediatr Dent. 2020;13(Suppl 1):S115-S118. doi: 10.5005/jp-journals-10005-1875.
10
[Relation between Abt-Letterer-Siwe disease, the eosinophilic granuloma of the bones (the eosinophilic granuloma) and Hand-Schüller-Christian disease].[阿-莱-施病、骨嗜酸性肉芽肿（嗜酸性肉芽肿）与汉-许-克病之间的关系]
Medizinische. 1955 Jul 23(29-30):1019-25.

引用本文的文献

1
Congenital self-healing reticulohistiocytosis: An atypical presentation acquired in a 10-month-old.先天性自愈性网状组织细胞增生症：一名10个月大婴儿的非典型表现。
Clin Case Rep. 2022 Aug 18;10(8):e6227. doi: 10.1002/ccr3.6227. eCollection 2022 Aug.

本文引用的文献

1
Temporal bone involvement in Hand-Schuller-Christian disease.颞骨受累于汉-许-克病。
Otol Neurotol. 2015 Mar;36(3):e95-6. doi: 10.1097/MAO.0000000000000356.
2
Hand-Schüller-Christian disease.汉-许-克病
Indian J Dent Res. 2012 Nov-Dec;23(6):830-2. doi: 10.4103/0970-9290.111273.
3
Hand Schuller Christian disease.汉-许-克病
Indian J Med Paediatr Oncol. 2011 Jul;32(3):183-4. doi: 10.4103/0971-5851.92835.
4
Intralesional infiltration of corticosteroids in the treatment of localised langerhans' cell histiocytosis of the mandible Report of known cases and three new cases.皮质类固醇瘤内注射治疗下颌骨局限性朗格汉斯细胞组织细胞增多症：已知病例报告及三例新病例
Int J Oral Maxillofac Surg. 2005 Jul;34(5):571-5. doi: 10.1016/j.ijom.2004.10.020. Epub 2005 Jan 24.
5
HAND-SCHULLER-CHRISTIAN SYNDROME. REPORT OF A CASE.汉-许-克综合征。病例报告。
Indian J Pediatr. 1964 Aug;31:246-8. doi: 10.1007/BF02821644.
6
Imaging of soft tissue tumors.软组织肿瘤的影像学检查
Radiol Clin North Am. 1993 Mar;31(2):359-72.
7
Hand Schüller Christian disease.汉-许-克病
J Postgrad Med. 1980 Apr;26(2):138-41.

汉-许-克病：一例伴有口腔表现的罕见病例报告

Hand schuller christian disease: a rare case report with oral manifestation.

作者信息

Lalitha Ch, Manjula M, Srikant K, Goyal Stuti, Tanveer Shahela

机构信息

Senior Lecturer, Department of Oral Medicine and Radiology, Sri Sai College of Dental Surgery , Vikarabad,Telanagana, India .

Professor, Department of Oral Medicine and Radiology, Gandhi Hospitals , Hyderabad, India .

出版信息

J Clin Diagn Res. 2015 Jan;9(1):ZD28-30. doi: 10.7860/JCDR/2015/10985.5481. Epub 2015 Jan 1.

DOI:10.7860/JCDR/2015/10985.5481
PMID:25738095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4347186/
Abstract

Langerhan's Cell Histiocytosis (LCH) is disorders which include abnormalities that result from abnormal proliferation of langerhan's cells or their precursors. LCH is clinically classified into three types-eosinophilic granuloma, Hand Schuller Christian disease and Abt-Letterer- Siwe disease. It is usually manifested in childhood as well as in adulthood. The clinical manifestations are the result of the accumulation and infilteration of the langerhan cells in organs and tissues. Here is a rare case report of 6-year-old boy with extraoral manifestation of exopthalmic right eye and oral manifestation of mobility of teeth and with typical radiological findings. Basing on the clinical, radiological and histopathological examination the diagnosis of Hand Schuller Christian Disease was given.

摘要

朗格汉斯细胞组织细胞增多症（LCH）是一类疾病，包括由朗格汉斯细胞或其前体细胞异常增殖导致的异常情况。LCH临床分为三种类型——嗜酸性肉芽肿、汉-许-克病和勒-雪病。它通常在儿童期和成年期均可出现。临床表现是朗格汉斯细胞在器官和组织中积聚及浸润的结果。本文报告一例罕见病例，一名6岁男孩，表现为右眼眼球突出的口外症状以及牙齿松动的口腔症状，并伴有典型的影像学表现。基于临床、影像学和组织病理学检查，诊断为汉-许-克病。