Gentry R R, Rust R S, Lohr J A, Alford B A
Pediatr Radiol. 1983;13(4):236-8. doi: 10.1007/BF00973165.
Infantile cortical hyperostosis (ICH), or Caffey's disease, first reported by Caffey and Silverman in 1945, is a benign condition characterized radiographically by corticoperiosteal thickening of bone with subperiosteal new bone formation. Sites of occurrence vary, with the mandible being involved in 75%-80% of cases. The following is a case report of ICH limited to four contiguous ribs with no evidence of mandibular involvement.
婴儿骨皮质增生症(ICH),即卡菲氏病,于1945年由卡菲和西尔弗曼首次报道,是一种良性病症,其影像学特征为骨皮质骨膜增厚并伴有骨膜下新骨形成。发病部位各异,75%-80%的病例累及下颌骨。以下是一例局限于四根相邻肋骨且无下颌骨受累证据的婴儿骨皮质增生症病例报告。