Ethunandan Madanagopalan, Khosla Nalin, Tilley Elizabeth, Webb Andrew
Queen Alexandra Hospital, Cosham, Portsmouth, United Kingdom.
J Craniofac Surg. 2004 Nov;15(6):1062-5. doi: 10.1097/00001665-200411000-00038.
Melorheostosis is a rare bone disorder, usually affecting the long bones and adjacent soft tissue. It was originally described by Leri and Joanny in 1922, after its classic x-ray features of flowing hyperostosis resembling dripping candle wax. There have been fewer than 10 reported cases of craniofacial involvement, and in most instances these have also involved the appendicular skeleton. The authors report a case of melorheostosis with isolated craniofacial involvement, describe the clinical course and radiologic and histologic features, and review the pertinent literature.
肢骨纹状肥大是一种罕见的骨病,通常累及长骨及相邻软组织。1922年,Leri和Joanny首次对其进行描述,因其典型的X线特征为骨质增生如滴蜡状。据报道,颅面部受累的病例少于10例,且多数情况下还累及附属骨骼。作者报告了一例孤立性颅面部受累的肢骨纹状肥大病例,描述了其临床病程、放射学和组织学特征,并复习了相关文献。