Caffey Disease with Raised Immunoglobulin Levels and Thrombocytosis
Overview
Affiliations
Infantile cortical hyperostosis (Caffey disease) is characterized by radiological evidence of cortical hyperostosis, soft tissue swellings, fever and irritability. We report a case of Caffey disease highlighting its presentation with thrombocytosis and high serum immunoglobulin level to alert physicians to use steroids cautiously in view of the known thrombocythemic effect of the drug. Raised Immunoglobulin also suggests that this syndrome could be infectious in origin.
Caffey's disease in disguise: a child abuse mimic.
Gupta H, Choudhary B BMJ Case Rep. 2024; 17(2).
PMID: 38331449 PMC: 10859985. DOI: 10.1136/bcr-2023-256998.
Caffey Disease in Infancy: A diagnostic dilemma for primary care physicians.
Siddiqui S, Siddiqui G, Maurya M, Shrivastava A, Singh M Sultan Qaboos Univ Med J. 2020; 20(1):e109-e111.
PMID: 32190379 PMC: 7065700. DOI: 10.18295/squmj.2020.20.01.017.
Caffey disease or infantile cortical hyperostosis: a case report.
Kutty N, Thomas D, George L, John T Oman Med J. 2011; 25(2):134-6.
PMID: 22125716 PMC: 3215490. DOI: 10.5001/omj.2010.36.
Infantile cortical hyperostosis and COL1A1 mutation in four generations.
Cerruti-Mainardi P, Venturi G, Spunton M, Favaron E, Zignani M, Provera S Eur J Pediatr. 2011; 170(11):1385-90.
PMID: 21567126 PMC: 3197908. DOI: 10.1007/s00431-011-1463-0.