Acrodermatitis Continua

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  • A variant of pustular psoriasis that has a persistent, relapsing course. Classified as a noninfectious neutrophilic dermatosis; acropustular eruption with a predilection for distal digits characterized by sterile pustules; early nail involvement
  • Synonym(s): acrodermatitis continua of Hallopeau; acrodermatitis perstans; dermatitis repens; pustular acrodermatitis

Description

  • Acute manifestations
    • Formation of multiple, sterile, painful pustules that have an erythematous base located surrounding and under the nail(s) that coalesce to form polycyclic “lakes of pus,” which subsequently rupture and crust
  • Chronic sequelae
    • Nail changes: paronychia, onychodystrophy, onycholysis, onychomadesis, and anonychia
    • Scaling of the nail bed and periungual skin
    • Sclerosis or atrophy of soft tissue adjacent and deep to nail bed
    • Osteolysis of underlying bone, particularly distal phalanges
  • Distribution
    • Typically affect distal extremities, affecting 1 to 2 digits, most frequently the 1st digits of the hands; can involve all fingers and toes
    • Predilection for dorsal surfaces of hands and feet
    • Spare the central palmar/plantar regions
    • Rarely spread proximally to involve feet, ankles, hands, and forearms. Isolated proximal psoriatic plaques are rare.

Epidemiology

  • Exceedingly rare: Only case studies and series are available.
  • Female predominance
  • Predominantly in adults but also seen in children: observed in 4.7% cases of infantile psoriasis in one series

Etiology and Pathophysiology

  • Immune dysregulation: Acute-phase reactants such as IL-1 and IL-36 likely play a role in pathogenesis (1).
  • In some instances, digital trauma or infection may be an inciting event.

Genetics

  • Reported associations with mutations in the IL36RN gene, which codes for the IL-36 receptor antagonist and is a cause of familial generalized pustular psoriasis (1,2)
  • No observed relationship with plaque psoriasis–associated alleles HLA-B13, HLA-B17, or HLA-BW37

Risk Factors

  • History of psoriasis, particularly pustular variant
  • Digital trauma
  • Local infection
  • Smoking may contribute to exacerbations.

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