Suppr超能文献

眶下区域皮肤型罗萨伊-多夫曼病复发

Cutaneous Rosai-Dorfman disease recurrence in infraorbital region.

作者信息

Lu Li-yan, Ju Wu-tong, Cai Ming, Lu Xiao-feng

机构信息

Department of Oral and Maxillofacial Surgery, Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai Key Laboratory of Stomatology, Shanghai, China.

出版信息

J Craniofac Surg. 2012 Sep;23(5):e509-10. doi: 10.1097/SCS.0b013e318266fb64.

Abstract

Rosai-Dorfman disease (RDD), also named sinus histiocytosis with massive lymphadenopathy, is a rare, idiopathic, and benign disorder that classically presents as a painless massive bilateral cervical lymphadenopathy. In cases of extranodal presentations, such as cutaneous RDD, it may not involve the classic manifestation. The diagnosis is usually made by histopathologic analysis. Surgery is suggested in the cases of significant cosmetic deformity or when there is fatal or functional obstruction. We reported a case of extranodal RDD that recurred in the infraorbital region postoperatively.

摘要

罗萨伊-多夫曼病(RDD),也称为伴有巨大淋巴结病的窦性组织细胞增多症,是一种罕见的、特发性的良性疾病,典型表现为无痛性双侧颈部巨大淋巴结病。在结外表现的病例中,如皮肤型RDD,可能不涉及经典表现。诊断通常通过组织病理学分析做出。在存在明显美容畸形或有致命性或功能性梗阻的情况下建议进行手术。我们报告了1例结外RDD病例,该病例术后在眶下区域复发。

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