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Pulsed Dye Laser for Sensory Dysesthesias Associated With Chronic Radiation Dermatitis

October 2026 | Volume 25 | Issue 10 | 968 | Copyright © October 2026


Published online September 22, 2026

Danny Linggonegoro MD, Bernice Kwong MD, Kelsey Elizabeth Hirotsu MD

Department of Dermatology, Stanford University School of Medicine, Stanford, CA

Abstract
Chronic radiation dermatitis (CRD) is a long-term complication of radiation therapy, typically manifesting as scarred atrophic plaques with telangiectasias. In some cases, patients report persistent sensory dysesthesias such as burning, stinging, and pruritus. These symptoms are underrecognized and likely underreported but can significantly impair quality of life and are often refractory to conventional therapies. Pulsed dye laser (PDL) has demonstrated efficacy in treating CRD-associated telangiectasias, but its role in alleviating sensory symptoms has not been reported.

We report 2 breast cancer patients with treatment-resistant CRD and debilitating dysesthesias who experienced substantial symptom improvement following PDL therapy. The first patient presented with a decade-long nonhealing chest wall wound and refractory pruritus. She underwent ten sessions of subpurpuric PDL at 6-week intervals, in combination with advanced wound care, and achieved complete wound healing and sustained relief of pruritus and skin fragility. The second patient presented with a burning erythematous axillary plaque present for three years. She underwent four PDL sessions at five-week intervals and reported her first meaningful reduction in burning immediately after the initial treatment, with nearly complete resolution of dysesthesia by her final session despite persistent telangiectasias.

These cases suggest that PDL may offer a novel therapeutic option for CRD-associated dysesthesias, particularly when integrated with multidisciplinary care involving medical dermatology, laser specialists, and wound care. Larger, prospective studies are warranted to clarify PDL efficacy for CRD-related dysesthesias.

 

INTRODUCTION

Chronic radiation dermatitis (CRD) is a long-term complication of radiation therapy and usually presents as atrophic plaques with telangiectasias. In some cases, CRD can be associated with persistent sensory dysesthesias such as burning, stinging, and pruritus. These underrecognized and likely underreported symptoms can impair quality of life as they can cause discomfort, sleep disturbance, and emotional distress.1 In many cases, they are refractory to conventional therapies.

Pulsed dye laser (PDL) has been shown to improve telangiectasias in CRD; however, its potential to relieve CRD-associated dysesthesias has not been reported. Similar to rosacea, where neurovascular dysregulation is thought to contribute to burning and stinging sensations, CRD-related dysesthesias may also have a similar pathophysiology. In this small case series, we describe 2 breast cancer patients with treatment-resistant CRD whose sensory dysesthesias improved following a series of PDL treatments.

CASE SERIES

Case 1:
A 63-year-old woman with Fitzpatrick skin type III and stage IIB invasive ductal carcinoma of the left breast underwent modified radical mastectomy and adjuvant radiation therapy. The first course delivered 50.4 Gy in 28 fractions to the left chest wall, with adjacent supraclavicular and medial parasternal regions each receiving 45 Gy in 25 fractions. Six years later, she received a second course of 50 Gy in 20 fractions to the sternum due to recurrence. Two years after her second treatment, she developed CRD with telangiectatic plaques and recurrent skin breakdown with a persistent non-healing wound. Her associated symptoms included pruritus. A biopsy was performed given persistent ulceration to rule out malignancy, which showed epidermal ulceration with mixed inflammation and focal cytologic atypia compatible with chronic radiation changes.

Over seven years, she was evaluated at more than 50 dermatology visits and failed topical corticosteroids, calcineurin inhibitors, antifungals, doxepin, ruxolitinib, and intralesional triamcinolone.