Murphree D D, Anez L
Department of Community Health and Family Medicine, University of Florida Health Science Center, Jacksonville, 32208, USA.
J Fam Pract. 1996 Apr;42(4):401-3.
Infantile cortical hyperostosis (ICH), or Caffey's disease, has a low prevalence, is not easily recognized clinically, and is seldom reported in the primary care literature. A case of infantile cortical hyperostosis of the right mandible of a newborn is reported. Multiple radiographic tests, as well as bone biopsy, were necessary to establish a definitive diagnosis. The most striking features of this disease are presented, including the clinical and physical presentation, radiographic characteristics, and pathology.
婴儿骨皮质增生症（ICH），即卡菲氏病，发病率低，临床不易识别，在初级保健文献中鲜有报道。本文报告了1例新生儿右下颌骨婴儿骨皮质增生症的病例。为明确诊断，需要进行多项影像学检查及骨活检。文中介绍了该病最显著的特征，包括临床和体格表现、影像学特征及病理学表现。
