Caffey disease in an infant.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL BMJ Case Reports Pub Date : 2024-11-19 DOI:10.1136/bcr-2024-261909
Anupama Tandon, Fozia Raza, Rajesh Tandon, Anwer Alam
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Abstract

A previously healthy female infant was brought to the paediatrics outpatient department by her mother reporting increased irritability and swelling behind her left shoulder, accompanied by restricted movement in her left arm. The irritability had been present for the past 5 months, with swelling also noticed at that time, gradually increasing in size. On examination, a large, firm, immobile mass was detected on the left scapular region. The mass was tender to touch, without any hardening or induration of the overlying skin. The child was afebrile, and her vital signs were stable. Subsequent imaging revealed hyperostosis in the left scapula, along with swelling of the surrounding soft tissue. After ruling out conditions such as chronic osteomyelitis, Ewing's sarcoma, rhabdomyosarcoma, trauma or child abuse, chronic recurrent multifocal osteomyelitis and hypervitaminosis A, the findings pointed to Caffey disease. Although infantile cortical hyperostosis, or Caffey disease, is rare, it should be considered in the differential diagnosis of a bony swelling in a young child.

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婴儿卡菲病
一名原本健康的女婴被其母亲带到儿科门诊部,称她的烦躁情绪加重,左肩后部肿胀,并伴有左臂活动受限的症状。烦躁不安的症状已经持续了 5 个月,肿胀也是在那时发现的,并且逐渐增大。经检查,在左肩胛骨部位发现了一个巨大、坚实、无法移动的肿块。触摸肿块有触痛,其上的皮肤没有任何硬化或压痕。患儿无发热,生命体征平稳。随后的影像学检查发现左肩胛骨骨质增生,周围软组织肿胀。在排除了慢性骨髓炎、尤文氏肉瘤、横纹肌肉瘤、外伤或虐待儿童、慢性复发性多灶性骨髓炎和维生素A过多症等病症后,检查结果显示患的是卡菲氏病。虽然婴儿皮质增生症或卡菲病很罕见,但在幼儿骨质肿胀的鉴别诊断中应考虑到这一疾病。
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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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