Singla Amit, Silvera V Michelle, Ciarlini Pedro, Warf Benjamin C
Department of Neurosurgery, SUNY Upstate Medical University, Syracuse, New York, USA.
J Neurosurg Pediatr. 2012 Nov;10(5):406-10. doi: 10.3171/2012.8.PEDS12262. Epub 2012 Sep 14.
Dysplastic structural lesions within the fourth ventricle have been reported in patients with Chiari malformation type II (CM-II). The authors report the unique case of a 22-year-old patient with myelomeningocele who presented with progressive pain, decreasing hand function, and lower cranial nerve dysfunction in the context of a slowly enlarging intramedullary mass at the cervicomedullary junction. At surgery a multinodular mass attached to caudally displaced fourth ventricle choroid plexus was completely removed from an expanded central canal. The histopathological findings were consistent with dysplastic-reactive choroid plexus. Postoperatively the patient experienced relief of pain and improvement in hand strength. To the authors' knowledge, this is the first reported case in which dysplastic fourth ventricle choroid plexus was displaced caudally through the obex to become an intramedullary lesion at the cervicomedullary junction. Its subsequent slow enlargement with progressive neurological deficits may have been secondary to reactive inflammatory changes. For patients with myelomeningocele and CM-II, intramedullary dysplastic-reactive choroid plexus should be included in the differential diagnosis of mass lesions in this location.
已有报道称,II型Chiari畸形(CM-II)患者的第四脑室内存在发育异常的结构性病变。作者报告了一例独特病例,一名22岁患有脊髓脊膜膨出的患者,在颈髓交界处髓内肿块缓慢增大的情况下,出现进行性疼痛、手部功能减退和低位颅神经功能障碍。手术中,一个附着于尾侧移位的第四脑室脉络丛的多结节肿块从扩大的中央管中被完全切除。组织病理学检查结果与发育异常-反应性脉络丛一致。术后患者疼痛缓解,手部力量有所改善。据作者所知,这是首例报告的病例,其中发育异常的第四脑室脉络丛通过闩尾侧移位,成为颈髓交界处的髓内病变。其随后的缓慢增大并伴有进行性神经功能缺损,可能继发于反应性炎症变化。对于患有脊髓脊膜膨出和CM-II的患者,在此部位的肿块性病变鉴别诊断中应考虑髓内发育异常-反应性脉络丛。