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CASE REPORT
Year : 2016  |  Volume : 17  |  Issue : 3  |  Page : 196-198

Angiolymphoid hyperplasia with eosinophilia of oral mucosa in a child treated with imiquimod


Department of Dermatology, Government Stanley Medical College and Hospital, Chennai, Tamil Nadu, India

Correspondence Address:
Rashmi Singh
Department of Dermatology, Government Stanley Medical College and Hospital, Royapuram, Chennai - 600 001, Tamil Nadu
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2319-7250.179640

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Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare and idiopathic disorder of blood vessels which is common in head and neck area of middle-aged women. We report a case of angiolymphoid hyperplasia of lower lip in a 7-year-old child, confirmed by histopathological findings of hyperplastic lymphoid follicles, eosinophilia, and proliferation of vessels and positive staining with CD3 and CD20 in immunohistochemistry. Lesion was treated with imiquimod for 16 weeks following which it resolved completely. We present this case for the rarity of the case in this age group on an atypical rare site. To the best of our knowledge, this is the first reported case of ALHE on oral mucosa of a male child.


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