Anwar Mohammad, Eltayef Mohamed
Rheumatology, Hampshire Hospitals NHS Foundation Trust, Basingstoke, GBR.
Ophthalmology, Hampshire Hospitals NHS Foundation Trust, Basingstoke, GBR.
Cureus. 2022 Dec 18;14(12):e32656. doi: 10.7759/cureus.32656. eCollection 2022 Dec.
Langerhans cell histiocytosis (LCH) is a rare disease of the reticuloendothelial system. It is characterized by misguided differentiation of myeloid dendritic cell precursors. LCH most commonly presents in childhood and the clinical presentation is dependent on the site and extent of organ involvement. We report a case of orbital Langerhans cell histiocytosis in a 12-year-old boy who presented with left periorbital cellulitis with subsequent proptosis. He later underwent a successful left orbital-frontal-temporal craniotomy and is currently undergoing postoperative chemotherapy.
朗格汉斯细胞组织细胞增多症(LCH)是一种罕见的网状内皮系统疾病。其特征是髓样树突状细胞前体的分化异常。LCH最常见于儿童期,临床表现取决于器官受累的部位和程度。我们报告一例12岁男孩的眼眶朗格汉斯细胞组织细胞增多症,该男孩最初表现为左眶周蜂窝织炎,随后出现眼球突出。他后来成功接受了左眶-额-颞开颅手术,目前正在接受术后化疗。