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Caffey disease with raised immunoglobulin levels and thrombocytosis.
Indian J Pediatr ; 2008 Feb; 75(2): 181-2
Article in English | IMSEAR | ID: sea-79237
ABSTRACT
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.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Thrombocytosis / Female / Humans / Immunoglobulin G / Immunoglobulin M / Hyperostosis, Cortical, Congenital / Diagnosis, Differential / Infant / Mandible Type of study: Diagnostic study Language: English Journal: Indian J Pediatr Year: 2008 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Thrombocytosis / Female / Humans / Immunoglobulin G / Immunoglobulin M / Hyperostosis, Cortical, Congenital / Diagnosis, Differential / Infant / Mandible Type of study: Diagnostic study Language: English Journal: Indian J Pediatr Year: 2008 Type: Article