Atrophic lichen planus

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ORPHA:254449L43.8
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1Active trials5Specialists8Treatment centers

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Overview

Atrophic lichen planus is a rare clinical variant of lichen planus, a chronic inflammatory disorder that primarily affects the skin. In this subtype, the characteristic violaceous (purple-colored) papules and plaques of lichen planus are accompanied by atrophy, meaning thinning and wasting of the affected skin. The lesions typically appear as well-demarcated, slightly depressed patches with a whitish or violaceous hue, often surrounded by a hyperpigmented border. The skin becomes thin and fragile in affected areas. Atrophic lichen planus most commonly involves the lower extremities, trunk, and occasionally the scalp, where it may lead to scarring alopecia (permanent hair loss). It is classified under the broader category of lichen planus (ICD-10: L43.8, other lichen planus). The exact cause of atrophic lichen planus, like other forms of lichen planus, is not fully understood but is believed to involve a T-cell-mediated autoimmune response directed against basal keratinocytes in the skin. The condition may be associated with other autoimmune disorders, hepatitis C virus infection, and certain medications. Patients may experience mild itching or discomfort, though some lesions can be asymptomatic. The atrophic changes distinguish this variant from classic lichen planus and may sometimes be confused with other atrophic skin conditions such as morphea or lichen sclerosus. Treatment of atrophic lichen planus is similar to that of other lichen planus variants and is primarily aimed at reducing inflammation and managing symptoms. First-line therapy typically includes potent topical corticosteroids. For more widespread or refractory disease, options may include topical calcineurin inhibitors (such as tacrolimus), phototherapy (narrowband UVB or PUVA), or systemic immunosuppressive agents such as oral corticosteroids, methotrexate, or acitretin. The condition may follow a chronic relapsing course, and the atrophic changes can be permanent even after the inflammatory component resolves. Regular follow-up is recommended to monitor for complications and disease progression.

Also known as:

Inheritance

Multifactorial

Caused by a mix of several genes and environmental factors

Age of Onset

Adult

Begins in adulthood (age 18 or older)

Orphanet ↗NORD ↗

FDA & Trial Timeline

4 events
Jun 2025The Therapeutic Effect of Curcumin in Nanogels Compared to 0.1% FAO in the Management of Oral Lichen Planus

Chulalongkorn University — NA

TrialRECRUITING
May 2025Treatment Outcomes and Patient Satisfaction of Oral Lichen Planus Treatment

Dar Al Uloom University — PHASE2, PHASE3

TrialRECRUITING
Nov 2024Evaluation of Desmoglein-3 Autoantibodies in the Tissues of Oral Lichen Planus and Correlation with Disease Severity

Ain Shams University

TrialNOT YET RECRUITING
Oct 2023VALOR: Vaginal Atrophy & Long-term Observation of Recovery

Stratpharma AG — NA

TrialRECRUITING

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

Treatments

No FDA-approved treatments are currently listed for Atrophic lichen planus.

1 clinical trialare actively recruiting — trials can provide access to cutting-edge therapies.

View clinical trials →

Clinical Trials

1 recruitingView all trials with filters →

Specialists

5 foundView all specialists →
SP
Sally A ElHaddad, Assist. Prof
Specialist
PI on 1 active trial
PM
Philip Hall, MD
Specialist
PI on 1 active trial
EP
Enas Elgendy, ph.D
Specialist
PI on 2 active trials
MP
Majid Sanatkhani, Assistant Professor
Specialist
PI on 1 active trial1 Atrophic lichen planus publication
PP
Pirawish Limlawan, D.D.S., Ph.D.
Specialist
PI on 1 active trial

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 Atrophic lichen planus.

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Community

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Latest news about Atrophic lichen planus

Disease timeline:

New recruiting trial: VALOR: Vaginal Atrophy & Long-term Observation of Recovery

A new clinical trial is recruiting patients for Atrophic lichen planus

New recruiting trial: Treatment Outcomes and Patient Satisfaction of Oral Lichen Planus Treatment

A new clinical trial is recruiting patients for Atrophic lichen planus

New recruiting trial: The Therapeutic Effect of Curcumin in Nanogels Compared to 0.1% FAO in the Management of Oral Lichen Planus

A new clinical trial is recruiting patients for Atrophic lichen planus

Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

Rare disease caregiving can be isolating. Connect with counseling and peer support.

Family & Caregiver Grants

Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Common questions about Atrophic lichen planus

What is Atrophic lichen planus?

Atrophic lichen planus is a rare clinical variant of lichen planus, a chronic inflammatory disorder that primarily affects the skin. In this subtype, the characteristic violaceous (purple-colored) papules and plaques of lichen planus are accompanied by atrophy, meaning thinning and wasting of the affected skin. The lesions typically appear as well-demarcated, slightly depressed patches with a whitish or violaceous hue, often surrounded by a hyperpigmented border. The skin becomes thin and fragile in affected areas. Atrophic lichen planus most commonly involves the lower extremities, trunk, and

How is Atrophic lichen planus inherited?

Atrophic lichen planus follows a multifactorial inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Atrophic lichen planus typically begin?

Typical onset of Atrophic lichen planus is adult. Age of onset can vary across affected individuals.

Are there clinical trials for Atrophic lichen planus?

Yes — 1 recruiting clinical trial is currently listed for Atrophic lichen planus on UniteRare. See the clinical trials section on this page for phase, sponsor, and site details sourced from ClinicalTrials.gov.

Which specialists treat Atrophic lichen planus?

5 specialists and care centers treating Atrophic lichen planus are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.