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神经母细胞瘤与先天性巨结肠并存——神经嵴病的另一种表现形式?

Coexistent neuroblastoma and Hirschsprung's disease--another manifestation of the neurocristopathy?

作者信息

Gaisie G, Oh K S, Young L W

出版信息

Pediatr Radiol. 1979 Jul 24;8(3):161-3. doi: 10.1007/BF00973826.

Abstract

Abnormalities of neural crest development may be manifested in a wide variety of ways ranging from von Recklinghausen's disease to Sipple's syndrome -- pheochromocytoma and medullary thyroid carcinoma. We report here yet another manifestation -- coexistent multiple neuroblastomas and Hirschsprung's disease in a newborn. In a review of the English literature we have found the combination of neuroblastoma and Hirschsprung's disease recorded only once previously [2]. However, the relationship between the two diseases was not discussed. The two diseases may be at the extremes of a spectrum of neural crest development pathology, i.e., Hirschsprung's representing a deficiency and neuroblastoma representing malignant proliferation of cells of neural crest origin.

摘要

神经嵴发育异常可能以多种方式表现出来,从冯·雷克林豪森病到西普尔综合征——嗜铬细胞瘤和甲状腺髓样癌。我们在此报告另一种表现形式——一名新生儿同时存在多发性神经母细胞瘤和先天性巨结肠病。在查阅英文文献时,我们发现神经母细胞瘤和先天性巨结肠病的组合此前仅被记录过一次[2]。然而,这两种疾病之间的关系并未被讨论。这两种疾病可能处于神经嵴发育病理学谱系的两个极端,即先天性巨结肠病代表一种缺陷,而神经母细胞瘤代表神经嵴起源细胞的恶性增殖。

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