新生儿骨软骨瘤的消退：一例报告及文献综述
Resolving neonatal osteochondroma: a case report and literature review.
作者信息
Shaw B A
机构信息
Department of Surgery, University of California, San Francisco-Fresno School of Medicine, USA.
出版信息
Am J Orthop (Belle Mead NJ). 1996 Mar;25(3):226-8.
PMID:8775700
Abstract
We report a case of spontaneous resolution of a congenital osteochondroma in a child with metachondromatosis. We could find no reports of congenital or neonatal osteochondromas. Furthermore, reports of spontaneous resolution of osteochondromas are rare. We conclude that some of these radiologically benign lesions may be observed in very young patients.
摘要
我们报告了一例患有软骨瘤病的儿童先天性骨软骨瘤自发消退的病例。我们未找到先天性或新生儿期骨软骨瘤的相关报道。此外，骨软骨瘤自发消退的报道也很罕见。我们得出结论，在非常年幼的患者中可能会观察到一些这类放射学表现为良性的病变。
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