Bavbek M, Atalay B, Altinörs N, Caner H
Department of Neurosurgery, Baskent University Faculty of Medicine, Ankara, Turkey.
Acta Neurochir (Wien). 2004 Feb;146(2):165-7. doi: 10.1007/s00701-003-0182-3. Epub 2003 Dec 22.
Eosinophilic granuloma (EG) is a rare disease but is more common in adults than children. It's often self-limiting. Spinal involvement is rare. It is the localized and most benign form of Langerhans' cell histiocytosis (previously known as histiocytosis X), characterised by lytic lesions in one or more bones. Spontaneous resolution of vertebral body lesions is very rare. In this case, the patient had one EG in a cervical vertebra and a similar lesion in a lumbar vertebra. This case is important because it featured a symptomatic lesion in the cervical spine accompanied by an asymptomatic lesion in a lumbar vertebra. We treated the cervical lesion by surgical fusion and followed the lumbar lesion up conservatively, with the patient in a corset. After 8 years of follow-up, control MRI showed that the lumbar lesion had spontaneously resolved.
嗜酸性肉芽肿(EG)是一种罕见疾病,但在成人中比儿童更常见。它通常具有自限性。脊柱受累罕见。它是朗格汉斯细胞组织细胞增多症(以前称为组织细胞增多症X)的局限性且最良性的形式,其特征是在一块或多块骨骼中出现溶骨性病变。椎体病变自发消退非常罕见。在本病例中,患者颈椎有一处EG,腰椎有一处类似病变。该病例很重要,因为其特征是颈椎出现有症状的病变,同时腰椎有无症状病变。我们通过手术融合治疗颈椎病变,并对腰椎病变进行保守随访,让患者佩戴束腰。经过8年随访,对照MRI显示腰椎病变已自发消退。