Khanduri Sachin, Katyal Gaurav, Goyal Aakshit, Jain Shreshtha, Sabharwal Tushar, Chaudhary Mriganki
Radiodiagnosis, Era's Lucknow Medical College and Hospital.
Cureus. 2017 Apr 16;9(4):e1170. doi: 10.7759/cureus.1170.
Caffey's disease, also known as Infantile Cortical Hyperostosis, is a rare, self-limited, benign, inflammatory gene-related disorder of infants that causes bone changes, soft tissue swelling, and irritability. The mandible (75%), clavicles, and ulnae are the bones most frequently involved, others being long bones, lateral ribs, ilia with skull being the rarest. However, we report a case of a 5-month-old male diagnosed with Infantile cortical hyperostosis but with absent mandibular and clavicular involvement, thus depicting the unusual presentation of this disease.
卡菲氏病，又称婴儿皮质骨增生症，是一种罕见的、自限性的、良性的、与基因相关的婴儿炎症性疾病，可导致骨骼变化、软组织肿胀和易激惹。下颌骨（75%）、锁骨和尺骨是最常受累的骨骼，其他还有长骨、外侧肋骨、髂骨，颅骨受累最为罕见。然而，我们报告了一例5个月大的男性患儿，诊断为婴儿皮质骨增生症，但下颌骨和锁骨未受累，从而呈现出该病不寻常的表现。
