Literature DB >> 15695863

Infantile cortical hyperostosis.

Sourabh Dutta1, Naveen Jain, Anish Bhattacharya, Kanya Mukhopadhyay.   

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 as pyrexia of unknown origin, appearance on radionuclide bone scintigraphy and our unsatisfactory experience of treating it with Ibuprofen, a prostaglandin inhibitor.

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Year:  2005        PMID： 15695863

Source DB:  PubMed          Journal:  Indian Pediatr        ISSN： 0019-6061            Impact factor:   1.411


  4 in total

1.  Case 1: A four-month-old boy with bilateral arm swelling.

Authors:  Arushi Gahlot Saini; Sanjay Verma; Sudhanshu Grover; Deepti Suri; Surjit Singh
Journal:  Paediatr Child Health       Date:  2013-04       Impact factor: 2.253

Review 2.  Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature.

Authors:  Taichi Kitaoka; Yoko Miyoshi; Noriyuki Namba; Kohji Miura; Takuo Kubota; Yasuhisa Ohata; Makoto Fujiwara; Masaki Takagi; Tomonobu Hasegawa; Harald Jüppner; Keiichi Ozono
Journal:  Eur J Pediatr       Date:  2014-01-04       Impact factor: 3.183

3.  Caffey disease with raised immunoglobulin levels and thrombocytosis.

Authors:  T Sathish Kumar; Julius Xavier Scott; Leni Grace Mathew
Journal:  Indian J Pediatr       Date:  2008-02       Impact factor: 1.967

4.  Infantile cortical hyperostosis and COL1A1 mutation in four generations.

Authors:  Paola Cerruti-Mainardi; Giacomo Venturi; Marianna Spunton; Elena Favaron; Michela Zignani; Sandro Provera; Bruno Dallapiccola
Journal:  Eur J Pediatr       Date:  2011-05-13       Impact factor: 3.183
  4 in total

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