Tfifha Miniar, Gaha Mehdi, Mama Nadia, Yacoubi Mohamed Taher, Abroug Saoussen, Jemni Hela
Miniar Tfifha, Saoussen Abroug, Pediatrics Department, Sahloul University Hospital, Sousse 4054, Tunisia.
World J Clin Cases. 2017 Aug 16;5(8):344-348. doi: 10.12998/wjcc.v5.i8.344.
Langerhans cell histiocytosis (LCH) is a rare condition mostly seen in children and adolescents. Eosinophilic granuloma (EG) is one of its three clinical entities and is considered as a benign osteolytic lesion. Many reports of patients with spine histiocytosis are well documented in the literature but it is not the case of atlantoaxial localization. We report here a new observation of atlantoaxial LCH in a 4-year-old boy revealed by persistent torticollis. He was successfully treated with systemic chemotherapy and surgery. Inter-body fusion packed by autologous iliac bone was performed with resolution of his symptoms. It is known that conservative treatment is usually sufficient and surgery should be reserved for major neurologic defects in spine EG. In atlantoaxial lesion, surgical treatment should be frequently considered.
朗格汉斯细胞组织细胞增多症(LCH)是一种罕见疾病,多见于儿童和青少年。嗜酸性肉芽肿(EG)是其三种临床类型之一,被认为是一种良性溶骨性病变。文献中有许多关于脊柱组织细胞增多症患者的报道,但寰枢椎定位的情况并非如此。我们在此报告一例4岁男孩因持续性斜颈而发现的寰枢椎LCH新病例。他通过全身化疗和手术成功治愈。采用自体髂骨进行椎间融合,症状得以缓解。众所周知,保守治疗通常就足够了,手术应仅用于脊柱EG出现严重神经功能缺损的情况。对于寰枢椎病变,应经常考虑手术治疗。