Spontaneous regression of osteochondromas

Spontaneous regression of osteochondromas
复制标题

DOI:
10.1007/s00256-006-0235-9
复制
发表时间:
2007-06-01
期刊:
影响因子:
2.1
通讯作者:
Noguchi, Kazuko
Noguchi, Kazuko
中科院分区:
医学4区
文献类型:
--
作者:
Hoshi, Manabu;Takami, Masatsugu;Noguchi, Kazuko

文献摘要

被引文献

相似文献

骨软骨瘤的自然消退是一个罕见的事件。在这份报告中,两例自发消退的骨软骨瘤。第一个病例是一个孤立的骨软骨瘤的有蒂型涉及右肱骨近端在一个7岁的男孩。该病变在15个月的观察中消退。第二个病例是一个3岁的女孩,患有多发性骨软骨瘤病,其中右胫骨和左腓骨的无蒂骨软骨瘤消退超过33个月。对于典型的骨软骨瘤,特别是幼儿,仔细观察是可以接受的。
Spontaneous regression of an osteochondroma is an infrequent event. In this report, two cases with spontaneous regression of osteochondromas are presented. The first case was a solitary osteochondroma of the pedunculated type involving the right proximal humerus in a 7-year-old boy. This lesion resolved over 15 months of observation. The second case was a 3-year-old girl with multiple osteochondromatosis, in whom sessile osteochondromas of the right tibia and left fibula regressed over 33 months.The mechanism of this phenomenon is discussed with a review of previous reports. Regarding treatment, careful observation may be acceptable for typical osteochondromas, especially in young children.