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Case Report

Kimura’s Disease in A Bangladeshi Boy: A Very Rare Cause of Lymphadenopathy

M.M.Z. Islam* , M.M. Rahman** , M. Parvez*** , J. Ferdaus****

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Indian Journal of Trauma and Emergency Pediatrics 8(1):p 35-38, January - April 2016. | DOI: DOI: https://dx.doi.org/10.21088/ijtep.2348.9987.8116.6

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Abstract

 Kimura’s Disease is a rare chronic inflammatory disorder that characteristically manifests as enlargement of head and neck lymph nodes and salivary glands accompanied by eosinophilia and elevated serum IgE. It is a benign condition with unknown etiology and said to be predominantly seen in males of Asian descent. We are presenting here a clinically and histologically typical case of this disease in a 12 years old Bangladeshi boy. The diagnosis of Kimura’s Disease can be very difficult and misleading; it is important not to ignore histopathological characteristics.

Keywords: Lympadenopathy; Eosinophilia; Histopathology.


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DOI: DOI: https://dx.doi.org/10.21088/ijtep.2348.9987.8116.6

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