Ostrowski D M, Gilula L A
Brockwood Orthopedic Associates, Birmingham, Alabama.
J Hand Surg Br. 1992 Feb;17(1):108-12. doi: 10.1016/0266-7681(92)90024-v.
We present a detailed study of a 59-year-old white woman with mixed sclerosing bone dystrophy: the rare occurrence of two or more sclerosing bone dysplasias in a single subject. She exhibited features of osteopoikilosis, osteopathia striata and melorheostosis. The symptoms were primarily the result of the melorheostosis lesions which were distributed within the C6 sclerotome. This is an unusual case of mixed sclerosing bone dystrophy in that the upper extremity was the main site of involvement, instead of the usual symmetrical involvement of all limbs. The patient developed a recalcitrant lateral epicondylitis in the un-involved contralateral elbow that required surgical treatment.
我们报告了一例59岁白人女性患有混合性硬化性骨营养不良的详细研究病例：这是一种罕见的在单个个体中出现两种或更多种硬化性骨发育异常的情况。她表现出骨斑点症、条纹状骨病和骨蜡油样骨病的特征。症状主要是由分布在C6体节内的骨蜡油样骨病病变引起的。这是一例不寻常的混合性硬化性骨营养不良病例，因为主要受累部位是上肢，而非通常的四肢对称性受累。患者在未受累的对侧肘部发生了顽固性外侧上髁炎，需要手术治疗。
