Halo Seborrheic Keratosis in a Patient of Color With Vitiligo

January 2026 | Volume 25 | Issue 1 | 9523 | Copyright © January 2026


Published online December 15, 2025

Amanda Nwaopara MS, Cheryl M. Burgess MD FAAD

Center for Dermatology and Dermatologic Surgery, Washington, DC

Abstract
A 73-year-old woman with Fitzpatrick skin type V presented with a long-standing brownish-black, three-tone macule on the right anterior thigh that developed a sharply demarcated depigmented halo. She also exhibited depigmented patches on the buttocks, hands, and feet consistent with vitiligo. Horizontal excision with histopathology confirmed seborrheic keratosis (SK) without atypia. This case highlights that the halo phenomenon can occur in non-melanocytic lesions, including SK,1 a presentation that may mimic melanoma and complicate diagnosis in richly pigmented skin.2,3 We review halo SK, discuss dermoscopic–pathologic features that distinguish it from melanoma and adult-onset halo nevus, and summarize evidence-based therapies for coexisting vitiligo, including topical ruxolitinib 1.5% cream and narrowband UVB (NB-UVB).4,5

 

INTRODUCTION

Practice Points
  • Depigmented halos are not restricted to melanocytic lesions; SK can rarely display a halo and may clinically resemble melanoma.1,2
  • Dermoscopy of seborrheic keratosis is characterized by features such as milia-like cysts, comedo-like openings, a cerebriform sulcus–gyrus pattern, moth-eaten borders with irregular peripheral indentations, and sharp demarcation.2 However, melanoma clues include blue-black/blue-white structures and an atypical network. Recognition of these patterns guides biopsy decisions.2,6
  • In skin of color, overlapping dermoscopic findings (eg, clonal SK vs pigmented basal cell carcinoma) create diagnostic pitfalls, underscoring the need for biopsy when uncertain.3
  • For vitiligo, phase 3 and randomized evidence support topical ruxolitinib cream and NB-UVB, with both modalities applicable to patients with richly pigmented skin.4,5

CASE PRESENTATION

A 73-year-old woman with Fitzpatrick skin type V presented for progressive hypopigmentation. Depigmented patches began on the buttocks three years earlier, with later involvement of hands and feet. She also reported a stable, brownish-black, three-tone macule on the right anterior thigh present for nearly two decades, but within the past year, it developed an enlarging depigmented ring.

On examination, there was an 8-10 mm smooth, brownish-black, three-tone macule on the right anterior thigh that was encircled by a sharply bordered depigmented halo. Additional well-demarcated depigmented macules and patches were observed on the buttocks, hands, and feet.

A horizontal excision under local anesthesia was performed. Histopathology demonstrated classic SK morphology without atypia or malignancy, confirming a benign SK with a halo phenomenon.

The patient was reassured. Vitiligo management was discussed, including photoprotection, topical calcineurin inhibitors, NB-UVB phototherapy, and topical ruxolitinib 1.5% cream applied twice daily.4,5