神经纤维肉瘤作为神经纤维瘤病的并发症。

Neurofibromatosis Pub Date : 1989-01-01
V M Riccardi, P P Powell
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引用次数: 0

摘要

神经纤维肉瘤(NFS)在一般人群中很少见,但在von Recklinghausen神经纤维瘤病(NF-1)患者中发病率很高。在Baylor NF项目的693名NF-1患者中,24名患者(3.5%)发展为NFS或其变体之一。24例患者中有9例在参加该计划后3-94个月内因其他原因发生NFS。仅对这9例患者的关注表明,NF-1患者发展为NFS的相对风险是一般人群的10-10,000倍。此外,在NFS队列中,NF-1患者在30岁以下的可能性几乎是其两倍。
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Neurofibrosarcoma as a complication of von Recklinghausen neurofibromatosis.

Neurofibrosarcoma (NFS), which is rare in the general population, occurs with excessive frequency among patients with von Recklinghausen neurofibromatosis (NF-1). Among 693 patients with NF-1 enrolled in the Baylor NF Program, 24 patients (3.5%) developed NFS or one of its variant forms. Nine of the twenty-four patients developed NFS within 3-94 months after enrolling in the Program for other reasons. Focus on these 9 patients alone suggests that the relative risk for patients with NF-1 developing NFS is 10-10,000 times greater than for the general population. Also, in NFS cohorts, patients with NF-1 are almost twice as likely to be under 30 years of age.

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