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ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA

Therapeutic Approach

Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare vasoproliferative disorder that presents as single or multiple pink to red-brown papules or nodules. ALHE most commonly affects the head and neck areas, and less commonly the trunk, extremities, and genital areas. Extracutaneous involvement including the orbit, oral mucosa, parotid gland, colon, and bone have been reported. Despite its benign nature, AHLE can bleed with minimal trauma and is frequently accompanied by pain, itch, or a pulsing sensation. In certain instances, spontaneous regresson of lesions may occur with time. In the authors’ experience, surgical excision is commonly used as a first-line therapy, but local reoccurrence is quite variable. Other therapies are still experimental at this time. See Table 119-1.

Table 119-1Angiolymphoid Hyperplasia with Eosinophilia Treatment Table

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