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特发性钙化性椎间盘炎继发腰椎间盘突出症。

Lumbar intravertebral disc herniation secondary to idiopathic calcific discitis.

作者信息

Sadek Ahmed-Ramadan, Dare Christopher, McGillion Stephen, Nader-Sepahi Ali, Skiadas Vasileios

机构信息

Department of Neurosurgery, Wessex Neurological Centre, University Hospital Southampton NHS Foundation Trust , Southampton , UK.

Division of Clinical Neurosciences, School of Medicine, University of Southampton , Southampton , UK.

出版信息

Br J Neurosurg. 2019 Oct;33(5):586-590. doi: 10.1080/02688697.2017.1394445. Epub 2017 Oct 26.

Abstract

Calcific discitis is a well recognized entity in the paediatric population but more recently has been increasingly reported in adults. It typically involves the lower thoracic vertebrae and is of unknown aetiology. Herniation of the calcified fragment is rare but typically occurs out through the annulus fibrosus into the canal space. Herein we describe the first reported case of calcific discitis involving the lumbar vertebrae with subsequent herniation of the calcified disc into and through the anterior aspect of the L5 vertebra. The patient first presented with a history of right back pain and leg sciatica. Radiographic imaging demonstrated calcification within the L4/5 interspace, which was managed with simple analgesia. She subsequently re-presented 24-months later with worsening sciatica, right leg weakness and faecal incontinence. No evidence of cord or root compression was noted on MRI. However, an abnormality was noted at the anterior body of L5 with evidence of superior endplate depression and marrow signal change. Subsequent radionucleide bone studies confirmed a solitary focus of increased linear activity extending across the width of the L4-L5 interspace. Her symptoms were managed medically. Serial radiographic imaging demonstrated regression of the disc space calcification and healing of the L5 fracture. Despite its sinister presentation this condition was self-limiting. We describe the radiographic evolution of this pathology and postulate a putative hypothesis through which it may have arisen.

摘要

钙化性椎间盘炎在儿科人群中是一种广为人知的病症,但最近在成人中也有越来越多的报道。它通常累及下胸椎,病因不明。钙化碎片突出很少见,但通常通过纤维环突入椎管间隙。在此,我们描述了首例报道的累及腰椎的钙化性椎间盘炎病例,随后钙化椎间盘突入并穿过L5椎体的前方。患者最初表现为右背痛和腿部坐骨神经痛病史。影像学检查显示L4/5间隙内有钙化,采用单纯镇痛治疗。24个月后,她因坐骨神经痛加重、右腿无力和大便失禁再次就诊。MRI未发现脊髓或神经根受压的证据。然而,L5椎体前缘发现异常,表现为上终板凹陷和骨髓信号改变。随后的放射性核素骨扫描证实,在L4-L5间隙宽度上有一个孤立的线性活性增加灶。她的症状采用药物治疗。系列影像学检查显示椎间盘间隙钙化消退,L5骨折愈合。尽管表现凶险,但这种情况是自限性的。我们描述了这种病理的影像学演变,并提出了一种可能的发病假说。

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