Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disorder characterized by vascular proliferation, eosinophilia in peripheral blood samples and lymphocytosis. The etiology is unknown; this rare condition is generally seen in women. It often presents as multiple, grouped red nodules in the periauricular region, scalp line and neck. Numerous therapeutic approaches have been tried for ALHE including destructive techniques such as electrodesiccation, cryotherapy, surgical excision, radiotherapy or laser (argon, CO(2), pulse dye). We present an ALHE case that was treated successfully by using topical imiquimod cream.

Download full-text PDF

Source
http://dx.doi.org/10.1159/000106581DOI Listing

Publication Analysis

Top Keywords

angiolymphoid hyperplasia
8
hyperplasia eosinophilia
8
eosinophilia treated
4
treated imiquimod
4
imiquimod case
4
case report
4
report angiolymphoid
4
eosinophilia alhe
4
alhe rare
4
rare disorder
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!