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先天性椎管内神经母细胞瘤系少见肿瘤。偶尔,它的X 线像如此特殊,以至只靠平片即可确诊。文内病例为3周半的女孩,自出生就有左侧腹部肿块及右下肢麻痹。腰骶椎平片显椎弓根间距增宽及平于腰椎1-3部位椎管内不规则形及点状钙化。生后第29天切除肿瘤。组织学证实为神经母细胞瘤。在32年间无复发。作者复习文献中的21例神经母细胞瘤,仅Bodian 氏的1例于椎管内有可疑钙化。年长后,此等病变具椎管内钙化已为众所周知。但这种钙化尚未见报道于先天性椎管内神经母细胞瘤。本文病例显示的这种特征性椎管内钙化未
Congenital spinal neuroblastoma is a rare tumor. Occasionally, its X-ray is so special that it can be confirmed only by plain film. The text in the case of 3 weeks and a half girls, since the birth of the left abdominal mass and paralysis of the right lower limb. Lumbar and sacral plain radiographs were widened pedicle spacing and flat in the lumbar 1-3 irregular intracranial and punctate calcification. The tumor is removed on the 29th day after birth. Histologically confirmed as neuroblastoma. No recurrence in 32 years. The authors reviewed 21 patients with neuroblastoma in the literature, and only 1 patient with Bodian’s disease had suspicious calcification in the spinal canal. Elderly, these lesions with intracranial calcification has been well known. However, this calcification has not been reported in congenital spinal neuroblastoma. This characteristic case of intracranial calcification shown in this case has not