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伴有巨大淋巴结病的窦性组织细胞增多症(罗萨伊-多夫曼病)一例出现面部不对称并累及鼻和眼眶。

Facial asymmetry with nasal and orbital involvement in a case of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease).

作者信息

El-Banhawy Omar A, Farahat Hassan G, El-Desoky Ibrahiem

机构信息

Department of otorhinolaryngology, Faculty of Medicine, El Menoufyia University, El Menoufyia, Egypt.

出版信息

Int J Pediatr Otorhinolaryngol. 2005 Aug;69(8):1141-5. doi: 10.1016/j.ijporl.2005.02.021. Epub 2005 Apr 7.

Abstract

Sinus histiocytosis with massive lymphadenopathy or "Rosai-Dorfman"s syndrome is a rare benign disease of unknown etiology, usually seen in younger patients. A 12-year-old boy of the disease presented with facial asymmetry, massive lymphadenopathy, nasal and orbital manifestation is reported. Diagnosis was performed by superficial lymph node biopsy. No immunodeficiency was found. Local excision of the orbital lesion and endonasal endoscopic resection of the disease from nasal, paranasal sinuses, and nasopharynx was achieved effectively. The clinical presentation, histologic characteristics, pathogenesis and treatment of this case is discussed. This is the first reported case, to the best of our knowledge, of the disease to be associated with facial asymmetry.

摘要

伴有巨大淋巴结病的窦组织细胞增生症或“罗萨伊-多夫曼”综合征是一种病因不明的罕见良性疾病,多见于年轻患者。本文报道了一名患有该疾病的12岁男孩,表现为面部不对称、巨大淋巴结病、鼻腔和眼眶病变。通过浅表淋巴结活检进行诊断。未发现免疫缺陷。有效地实现了眼眶病变的局部切除以及鼻腔、鼻窦和鼻咽部疾病的鼻内镜下切除。本文讨论了该病例的临床表现、组织学特征、发病机制及治疗。据我们所知,这是首例报道的与面部不对称相关的该疾病病例。

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