Despite its relevance and international recognition, the Fitzpatrick classification presents several methodological and biological limitations that call its accuracy into question. One of the main criticisms leveled against it is its inability to faithfully represent the true diversity of skin tones worldwide, particularly the darkest complexions. Indeed, the scale relies on a linear spectrum of pigmentation ranging from very fair (Type I) to very dark (Type VI), assuming that darker skin tones always tan and almost never burn. Yet, this is a dangerous oversimplification.
Contrary to what the Fitzpatrick classification suggests, dark skin can also get sunburned. Although melanin plays an essential photoprotective role, it does not offer complete protection against UV-induced damage, especially during prolonged or intense exposure. Hence, individuals with phototypes V or VI can develop erythematous lesions or cumulative photodamage, yet these manifestations are often underestimated or poorly recognized by both patients and some healthcare professionals. This false sense of security among dark-skinned individuals has significant clinical consequences. Believing that they are not at risk from sun exposure, many neglect sun protection and do not check their moles, a behavior that contributes to increased mortality from skin cancer in dark-skinned populations.
Furthermore, with increasing migration and genetic mixing, these biases become even more problematic. The Fitzpatrick system, based on a primarily Eurocentric categorization, no longer manages to reflect the genetic and pigmentary complexity of contemporary populations. The later-added phototypes V and VI—introduced to include Asian, Indian, and African skin tones—are insufficient to cover intragroup variability, meaning the multiple shades and skin reactivities exhibited by individuals within the same category.
Modern dermatology today aims to move beyond this approach by developing more inclusive, quantitative models, integrating objective measurements of pigmentation, UV sensitivity, and the skin’s inflammatory response. The goal is to better tailor medical and aesthetic interventions to the biological reality of each individual’s skin — rather than to a pigmentary typology inherited from the 1970s which, although insightful, remains incomplete.
The Fitzpatrick classification remains a useful tool but must be supplemented by a more inclusive and individualized approach to accurately reflect the true diversity of skin types.