Aug 2026· Clinical, Cosmetic and Investigational Dermatology· Vol 19, pp. 1-11· 0 citations· 42 references
Medicine
TL;DR
This narrative review systematically synthesizes current knowledge on the epidemiology, unique clinical presentations, and the specific pathophysiological mechanisms underlying this recalcitrant variant to provide a nuanced, evidence-based understanding of acral vitiligo to guide clinical management.
Abstract
Abstract Acral vitiligo, a distinct subtype predominantly affecting the distal extremities (hands and feet), presents significant clinical challenges due to its treatment resistance and profound psychosocial impact. This narrative review systematically synthesizes current knowledge on the epidemiology, unique clinical presentations, and the specific pathophysiological mechanisms underlying this recalcitrant variant. We critically appraise recent advances in diagnosis and treatment, integrating findings from clinical studies, experimental researches, and case reports. The central aim is to provide a nuanced, evidence-based understanding of acral vitiligo to guide clinical management. We critically evaluate contemporary treatment modalities, including the emerging roles of Janus kinase (JAK) inhibitors and biologic agents, while also addressing the crucial dimension of psychosocial burden. Finally, we delineate key knowledge gaps—particularly the lack of acral‑specific outcome measures and head‑to‑head comparative trials—and propose future research directions to improve outcomes for patients with this therapeutically orphaned subtype.
INTRODUCTION
Erythromelalgia (EM) is a rare clinical entity predominantly affecting distal extremities characterized by episodes of painful burning erythema, often precipitated by heat and exercise. Despite its significant impact on quality of life, no guidelines exist for treatment of this complex disorder, and manage...
Jumana Aldhalaan, J. Sartori-Valinotti, M. D. Davis et al.· Expert Opinion on Pharmacoth...· 0 citations
Aim: To summarize current clinical knowledge on the manifestations, organ-specific complications, and medical management of VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic syndrome).
Methods: A review of peer-reviewed clinical cohorts, registry evaluations and consensus reports published between 2020 an...
Marcin Sękulski, Martyna Mrożek, Igor Zydlewski et al.· International Journal of Inn...· 0 citations
Alopecia, commonly referred to as hair loss, is a prevalent dermatological condition that affects individuals of different ages and may have considerable physical, psychological, and social consequences. It is a multifactorial disorder associated with genetic, hormonal, immune-mediated, inflammatory, nutritional, syste...
Pratheeksha, Salma Banu Mohammed Javed, Fathimath Shabeeba et al.· International Journal of Pha...· 0 citations
VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic) syndrome is a newly recognized, ubiquitin-activating enzyme E1 (UBA1)-mediated autoinflammatory disorder characterized by treatment-refractory systemic inflammation and diverse cutaneous findings. Dermatologists are uniquely positioned to facilitate early...
Maria V. Kaltchenko, Saloni Patel, A. Srikumar et al.· Journal of American Academy...· 0 citations
Background Vitiligo is a chronic autoimmune disease characterized by depigmented patches on the skin. Despite the availability of several therapeutic options, treatment outcomes remain variable, particularly in extensive or refractory disease. Tofacitinib, a Janus kinase (JAK) inhibitor, has emerged as a potential ther...
Mansooreh Ahmadkhani, Tahereh Dara, Mohsen Zabihi et al.· Clinical, Cosmetic and Inves...· 0 citations
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