Pigmented Basal Cell Carcinoma in Skin of Color: A Systematic Review of the Literature

July 2026 | Volume 25 | Issue 7 | 605 | Copyright © July 2026


Published online June 30, 2026

Victoria S. Humphrey MDa, Adewunmi Adelaja MD PhDa, Balaji Jothishankar MD MBAb, Ramone F. Williams MD MPhilc

aHarvard Combined Dermatology Residency Training Program, Boston, MA
bLahey Hospital and Medical Center, Department of Dermatologic Surgery, Burlington, MA
cMassachusetts General Hospital, Dermatologic Surgery Unit, Boston, MA

Abstract
Background: Though basal cell carcinoma (BCC) is most often studied in Fitzpatrick Skin Types (FST) I-III, BCC in skin of color (SOC) is characterized by unique clinical features and a propensity toward pigmentation. While cutaneous malignancy occurs with decreased frequency in FST IV - VI, the diagnosis is generally associated with disproportionately increased morbidity and mortality. Accordingly, it is increasingly vital for dermatologists to recognize clinical presentations of skin cancer in individuals with SOC to improve outcomes and mitigate gaps in care.
Objective: We systematically reviewed the literature regarding pigmented basal cell carcinoma (pBCC) in individuals with SOC.
Methods and Materials: The keywords “pigmented basal cell carcinoma” and “pBCC” were independently combined with “Asian,” “Black,” “Hispanic,” “Latinx,” “skin of color,” and “SOC” to perform a PubMed/MEDLINE search.
Results: Based on the selected search terms, 26 unique articles were identified. Of these, 16 articles met the inclusion criteria for full-text screening.
Conclusion: Pigmented BCC is more common in those with SOC and can be clinically challenging to diagnose. As evidence suggests that pBCC confers a favorable prognosis, efforts to standardize reporting and formalize sub-classification should be considered. Furthermore, as the existing literature is primarily retrospective with small sample sizes, larger prospective studies would be valuable additions to the literature and aid in shedding light on disparate outcomes associated with cutaneous malignancy in skin of color.

INTRODUCTION

Recent data show that basal cell carcinoma (BCC) is the most common cutaneous malignancy in all races.1,2 Though BCC is most often studied in Fitzpatrick skin types (FST) I-III, BCC in skin of color (SOC) is characterized by unique clinical features and a propensity toward pigmentation. Herein, we present a systematic review of pigmented basal cell carcinoma (pBCC) in individuals with SOC.

SOC is defined as FST IV, V, or VI in individuals of Latinx, Black, or Asian descent.3,4 While skin cancer occurs with a decreased frequency in individuals with skin of color, the diagnosis is generally associated with disproportionately high morbidity and mortality.5,6 Poor outcomes in individuals with skin of color are often attributed to delayed diagnosis and more advanced disease in the setting of atypical clinical presentations.5,6 Socioeconomic disparities, environmental factors, as well as explicit and implicit bias within the healthcare system, play decisive roles as well. Dermatologists need to recognize clinical presentations of skin cancer in individuals with skin of color to improve outcomes and mitigate gaps in care.

MATERIALS AND METHODS

A systematic review was completed following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A search for peer-reviewed articles was conducted on PubMed/MEDLINE with no publication date restriction. The terms "pigmented basal cell carcinoma" and "pBCC" were independently combined with "Asian," "Black," "Hispanic," "Latinx," "skin of color," and "SOC" using the Boolean operator "AND."

Human studies and studies written in the English language were included. In vitro, cadaver, and animal studies were excluded, as well as duplicates and articles for which the complete text was unavailable. Additional studies addressing skin cancer in men and women with skin of color were included per a discriminant review of article references. Data extraction was performed following a full-text review of eligible articles (Figure 1).