Acrodermatitis continua of Hallopeau

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ORPHA:163931L40.2
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UniteRare data is sourced from FDA.gov, ClinicalTrials.gov, Orphanet, OMIM, and NORD.
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Overview

Acrodermatitis continua of Hallopeau (ACH), also known as acrodermatitis perstans or dermatitis repens, is a rare, chronic, and often treatment-resistant form of localized pustular psoriasis. It is classified under pustular psoriasis (ICD-10: L40.2) and is characterized by sterile (non-infectious) pustular eruptions that typically begin on the tips of the fingers and toes, often following local trauma or infection. The pustules recur persistently and can spread proximally along the digits and occasionally to other areas of the skin. The disease primarily affects the skin and nails of the distal extremities. Key clinical features include painful, sterile pustules on the fingertips and toes that dry and reform in a continuous cycle, leading to progressive nail dystrophy and eventual nail loss (anonychia). Over time, the chronic inflammation can cause atrophy of the underlying soft tissue and even osteolysis (bone resorption) of the distal phalanges, resulting in significant functional impairment and disability. The skin of affected digits becomes erythematous, glazed, and scaly. The condition can be extremely painful and debilitating, significantly impacting quality of life. Treatment of acrodermatitis continua of Hallopeau is challenging, as the condition is notoriously resistant to many therapies. Topical treatments including potent corticosteroids, calcipotriol, and tacrolimus may provide partial relief. Systemic therapies such as acitretin, methotrexate, and cyclosporine have been used with variable success. More recently, biologic agents targeting tumor necrosis factor-alpha (TNF-α inhibitors such as infliximab and adalimumab), interleukin-17 (secukinumab, ixekizumab), and interleukin-36 receptor (spesolimab) have shown promising results in refractory cases. Phototherapy (PUVA) and photodynamic therapy have also been reported as adjunctive options. Early and aggressive treatment is important to prevent irreversible nail and bone damage.

Inheritance

Sporadic

Usually appears on its own, not inherited from a parent

Age of Onset

Adult

Begins in adulthood (age 18 or older)

Orphanet ↗NORD ↗

FDA & Trial Timeline

1 event
Sep 2021International Rare And Severe Psoriasis Expert Network

University Hospital, Basel, Switzerland

TrialRECRUITING

Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Treatments

No FDA-approved treatments are currently listed for Acrodermatitis continua of Hallopeau.

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No actively recruiting trials found for Acrodermatitis continua of Hallopeau at this time.

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No specialists are currently listed for Acrodermatitis continua of Hallopeau.

View NORD Rare Disease Centers ↗Undiagnosed Disease Network ↗

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Acrodermatitis continua of Hallopeau.

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Community

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Latest news about Acrodermatitis continua of Hallopeau

Disease timeline:

New recruiting trial: International Rare And Severe Psoriasis Expert Network

A new clinical trial is recruiting patients for Acrodermatitis continua of Hallopeau

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Common questions about Acrodermatitis continua of Hallopeau

What is Acrodermatitis continua of Hallopeau?

Acrodermatitis continua of Hallopeau (ACH), also known as acrodermatitis perstans or dermatitis repens, is a rare, chronic, and often treatment-resistant form of localized pustular psoriasis. It is classified under pustular psoriasis (ICD-10: L40.2) and is characterized by sterile (non-infectious) pustular eruptions that typically begin on the tips of the fingers and toes, often following local trauma or infection. The pustules recur persistently and can spread proximally along the digits and occasionally to other areas of the skin. The disease primarily affects the skin and nails of the dist

How is Acrodermatitis continua of Hallopeau inherited?

Acrodermatitis continua of Hallopeau follows a sporadic inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Acrodermatitis continua of Hallopeau typically begin?

Typical onset of Acrodermatitis continua of Hallopeau is adult. Age of onset can vary across affected individuals.