Kushner B H, Hajdu S I, Helson L
J Clin Oncol. 1985 Jan;3(1):117-20. doi: 10.1200/JCO.1985.3.1.117.
We report an unusual case of progressive disseminated neuroblastoma occurring in a child with a family history and stigmata of von Recklinghausen's disease. A review of the literature confirms the extreme rarity of finding these two neurocristopathies in a single individual and thus undermines the widely held notion of an association--genetic or otherwise--between these two entities. We propose that synchronous neuroblastoma and von Recklinghausen's disease is accounted for by chance alone and therefore represents a randomly occurring phenomenon.
我们报告了一例罕见的进行性播散性神经母细胞瘤病例,该病例发生在一名有冯·雷克林豪森病家族史和体征的儿童身上。文献回顾证实,在同一个体中发现这两种神经嵴病极为罕见,因此削弱了关于这两种疾病之间存在遗传或其他关联这一广泛观点。我们认为,同步发生的神经母细胞瘤和冯·雷克林豪森病只是偶然发生的,因此代表了一种随机出现的现象。