Bercau G, Gonzalez M, Afriat R, Lecolier B, de Kermadec S
Service de Gynécologie-Obstétrique, Hôpital Notre-Dame de Bon Secours, 6, Paris.
Ann Pediatr (Paris). 1991 Jan;38(1):15-8.
A very early case of infantile cortical hyperplasia (Caffey disease) is reported. The ultrasound examination performed at 22 weeks gestational age evidenced angulations of the long bones, leading to the diagnosis of lethal osteogenesis imperfecta. Hydrops fetalis developed and the pregnancy was terminated. The roentgenographic study of the fetus and results of pathological studies led to the correct diagnosis of Caffey disease. The difficulty of the diagnosis of these early forms of infantile cortical hyperostosis should be pointed out.
报告了一例非常早期的婴儿皮质增生症（卡菲病）。在孕22周时进行的超声检查显示长骨有角状改变，导致诊断为致死性成骨不全。随后出现胎儿水肿，遂终止妊娠。对胎儿的X线检查及病理研究结果得出了卡菲病的正确诊断。应当指出诊断这些早期婴儿皮质骨增生症的困难之处。
