Abstract

Background: Hidradenitis suppurativa is a chronic follicular occlusive disease in apocrine gland-bearing regions. Frequently refractory to conventional oral and topical treatments, it may require surgical intervention. Objective: To investigate the effectiveness of radiation therapy for refractory hidradenitis suppurativa. Methods and materials: Five patients with refractory Hurley stage II/III hidradenitis suppurativa were treated with radiation therapy to 13 affected sites. Electron beam radiation to a total dose of 7.5 gray was applied over 3 consecutive days. Results: The mean age of patients was 45 years; 80% had hidradenitis suppurativa for ≥ 6 years. Three patients had Hurley stage III; 2 had Hurley stage II. All had been treated previously with topical and oral antibiotics and other therapies, including surgery, radiation therapy, Nd:YAG laser therapy, and infliximab. No complete responses were observed, but 53% of the lesions had a partial response. Lesions in the axilla, gluteal, and inguinal areas had response rates of 100%, 67%, and 50%, respectively, compared to 0% for perineal lesions. Conclusions: Radiation therapy may be a promising treatment for refractory hidradenitis suppurativa. A prospective study is warranted to further evaluate response rates, define optimal dose fractionation schedules, and better understand the risk of long-term toxicity.

Highlights

  • Radiation therapy may be a promising treatment for refractory hidradenitis suppurativa

  • Hidradenitis suppurativa is a disfiguring skin condition characterized by recurring inflammatory and suppurative lesions in the flexural regions

  • It can have a tremendously detrimental impact on quality of life [1]. It is a part of the follicular tetrad that includes acne conglobata, dissecting cellulitis of the scalp, and pilonidal sinus [2]

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Summary

Introduction

Hidradenitis suppurativa is a disfiguring skin condition characterized by recurring inflammatory and suppurative lesions in the flexural regions (ie, the axillae, inframammary folds, and inguinal, perineal, and intergluteal areas). It can have a tremendously detrimental impact on quality of life [1]. Follicular hyperkeratosis and occlusion is theorized to be the primary etiologic factor, with apocrine involvement being secondary [3]. Multiple risk factors associated with hidradenitis suppurativa include endocrine causes, obesity, smoking and a genetic component [4]. Hidradenitis suppurativa is a chronic follicular occlusive disease in apocrine gland-bearing regions. Refractory to conventional oral and topical treatments, it may require surgical intervention

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