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:
Multifactorial
Caused by a mix of several genes and environmental factors
Adult
Begins in adulthood (age 18 or older)
FDA & Trial Timeline
4 eventsChulalongkorn University — NA
Dar Al Uloom University — PHASE2, PHASE3
Ain Shams University
Stratpharma AG — NA
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 →Treatment Centers
8 centersBaylor College of Medicine Rare Disease Center ↗
Baylor College of Medicine
📍 Houston, TX
🏥 NORDStanford Medicine Rare Disease Center ↗
Stanford Medicine
📍 Stanford, CA
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
🔬 UDNUCLA UDN Clinical Site ↗
UCLA Health
📍 Los Angeles, CA
🔬 UDNBaylor College of Medicine UDN Clinical Site ↗
Baylor College of Medicine
📍 Houston, TX
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDMayo Clinic Center for Individualized Medicine ↗
Mayo Clinic
📍 Rochester, MN
👤 Mayo Clinic Center for Individualized Medicine
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
Travel Grants
No travel grants are currently matched to Atrophic lichen planus.
Community
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Start the conversation →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.