Martino A M, Winfield J A
Department of Neurosurgery, Childrens Hospital of Michigan, Detroit.
Pediatr Neurosurg. 1990;16(6):321-5. doi: 10.1159/000120552.
Neurologic complications of sickle cell anemia are most commonly ischemic strokes secondary to sludging in cerebral arterioles. We, therefore, report a case of progressive paraparesis in a child with sickle cell anemia which was initially thought to be secondary to a spinal cord ischemic event. Further diagnostics demonstrated that the neurologic deficits were secondary to salmonella osteomyelitis and an epidural abscess, compressing the upper thoracic spinal cord at the T6 level. The diagnostic and radiological features which help to distinguish between bone infarct and osteomyelitis, both responsible for bone pain in sickle cell patients, are also presented. In particular, Tc-sulfur colloid bone marrow imaging is the most helpful test for distinguishing between these similarly presenting clinical entities, as early as 48 h after bone pain develops.
镰状细胞贫血的神经系统并发症最常见的是继发于脑小动脉内血液淤积的缺血性中风。因此,我们报告一例患有镰状细胞贫血的儿童出现进行性双下肢轻瘫的病例,该病例最初被认为继发于脊髓缺血事件。进一步的诊断表明,神经功能缺损继发于沙门氏菌骨髓炎和硬膜外脓肿,在T6水平压迫胸段脊髓上部。本文还介绍了有助于区分骨梗死和骨髓炎的诊断及影像学特征,这两种情况均可导致镰状细胞病患者出现骨痛。特别是,锝-硫胶体骨髓显像对于区分这些临床表现相似的疾病是最有帮助的检查,早在骨痛出现后48小时即可进行。