Open AccessAngiolymphoid Hyperplasia with Eosinophilia Involving the Occipital Artery: Case Report and Review of Literature
Author(s) -
Laia Fité-Trepat,
Míriam Martos-Fernández,
Margarita AlberolaFerranti,
Alba De Pablo-Garcia-Cuenca,
Coro BescósAtín
Publication year - 2017
Publication title -
journal of clinical and diagnostic research
Language(s) - English
Resource type - Journals
eISSN - 2249-782X
pISSN - 0973-709X
DOI - 10.7860/jcdr/2017/23323.9569
Subject(s) - angiolymphoid hyperplasia with eosinophilia , medicine , head and neck , lesion , surgical excision , radiology , surgery , dermatology
Angiolymphoid Hyperplasia with Eosinophilia (ALHE) is an atypical vascular tumour occurring primarily in the head and neck area, which must be distinguished from Kimura's disease. The lesions can appear as single or multiple grouped intradermal papules or subcutaneous nodules. We report a rare case of ALHE in a 57-year-old female with a large lesion of three nodules involving the right occipital artery which had a long term evolution and we treated it by surgical excision. The definitive histopathological diagnosis was ALHE. Our case report is accompanied by a discussion of clinical, radiological and histological features. Surgical excision with free margins is the treatment of choice but, even though ALHE is considered a benign condition, recurrence is common.