ORPHA:542643
Livedoid vasculopathy
Also known as: Livedo reticularis with summer ulcerations · Milian atrophie blanche · Segmental hyalinizing vasculitis
Publications
727
89.1th percentile
Trials
0
Interventional, condition-specific
Researchers
887
Distinct authors in sample
Gene link
—
Readiness
1/6
Stages with a signal
Clinical definition (Orphanet)
A rare vascular skin disease characterized by recurrent focal non-inflammatory thrombosis of dermal venulae, predominantly of the lower extremities, resulting in a cutaneous response manifested as pruritus and painful papules and erythematous plaques. The lesions evolve into hemorrhagic vesicles or bullae, which rupture and turn into painful ulcers merging into reticulate, confluent, geometric, and painful ulcerations. During a period of a few months, the ulcerations change to porcelain-white atrophic scars with punctate telangiectasia (so-called atrophie blanche). In active disease, lesions in different stages coexist.
How rare: How common this is has not been clearly measured.
Cross-references
Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.
- MONDO:0025514
- MeSH:D000090122
- UMLS:C0343081
Additional Mondo synonyms (2)
livedoid vasculitis · livedoid vasculopathy
Research stages
Trial readiness signals
Where this condition sits on an open-data research pipeline — not how close a treatment is, and not medical advice. Empty stages often mean “not in these databases under this Mondo ID,” not “impossible.”
1/6 stages with a signal
Research-stage checklist from open sources (GenCC, literature, Monarch when enriched, ClinicalTrials.gov). Not a prognosis or care recommendation.
- Gene identifiedNot found
No GenCC disease–gene assertion in this build
- LiteraturePresent
727 matched papers (440 in last 10 years) Source
- Phenotype characterisedNot checked
Not yet enriched from Monarch / HPO
- Animal modelNot checked
Not yet enriched from Monarch / Alliance
- Orphan designationNot checked
FDA/EMA orphan-drug designation not enriched yet
- Interventional trialNot found
No matched interventional trial under our ClinicalTrials.gov rules
Biology
Genes and phenotypes
Gene–disease validity from GenCC, plus phenotypes and animal models joined from Monarch Initiative via Mondo ID — not a clinical diagnosis aid.
Do we know what causes it?
Not yet — the cause hasn't been pinned down in GenCC.
No strong gene–disease assertion joined for this Orphanet entity.
Phenotypes (Monarch / HPO)
Not enriched in this build — Monarch phenotype joins were not run for this record.
Animal models (Monarch / Alliance)
Not enriched in this build.
Literature
Is anyone studying this?
727
727 papers have been published on this condition. That is a real research literature — still far smaller than common diseases (breast cancer: over 700,000 papers). Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=5449) is 41.
727 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 41 (publications denominator n=5449).
440 in the last 10 years · high confidence · 89.1th percentile (publications denominator)
Phrase hits: 727 · MeSH hits: 9
Who's working on it?
887
Distinct author names in 200 sampled papers — named people below.
Who's working on it?
No interventional trial matched this name; these authors publish on it in the sampled literature — a practical starting point for contact.
- 01Gao Y10 papers · 2025
Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Papers in Europe PMC - 02Jin H10 papers · 2024
Department of Dermatology, Peking Union Medical College Hospital (Dongdan campus), Chinese Academy of Medical Science and Peking Union Medical College, No.1 Shuaifuyuan Wangfujing Dongcheng District, Beijing, 100730, China. jinhongzhong@263.net.
Papers in Europe PMC - 03Criado PR6 papers · 2026
Dermatology Department of Hospital das Clínicas, University of Sao Paulo Medical School, São Paulo, Brazil.
Papers in Europe PMC - 04Moll S6 papers · 2024
Division of Hematology, Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina, United States.
Papers in Europe PMC - 05Erkan D5 papers · 2025
Barbara Volcker Center for Women and Rheumatic Diseases, Hospital for Special Surgery, New York, NY, United States.
Papers in Europe PMC - 06Eswaran H5 papers · 2024
Division of Hematology, Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC.
Papers in Europe PMC - 07Goerge T5 papers · 2025
Department of Dermatology, Division of Wound Healing/Phlebology, University Medical Center Münster, Münster, Germany.
Papers in Europe PMC - 08Liu Y5 papers · 2026
Department of Dermatology, Xiangya Hospital, Central South University, Changsha, China.
Papers in Europe PMC - 09Dissemond J4 papers · 2024
Department of Dermatology, Venereology and Allergology, University Medical Center Essen, Essen, Germany.
Papers in Europe PMC - 10Sciascia S4 papers · 2026
Department of Clinical and Biological Sciences, University Center of Excellence on Nephrologic, Rheumatologic and Rare Diseases (ERK-Net, ERN-ReConnect and RITA-ERN Member) with Nephrology and Dialysis Unit and Center of Immuno-Rheumatology and Rare Diseases (CMID), ASL Città Di Torino and University of Turin, Turin, Italy.
Papers in Europe PMC
Clinical research
Is a treatment being tested?
0
interventional trials for this specific condition
No interventional trial testing a treatment matched this specific condition name. 2 observational studies did — shown below because natural-history and cohort work can be an important step toward a trial.
Data as of 27 July 2026
No matched interventional trials. This is true for 73% of diseases in the trials denominator (5114 of 7003). Here are the researchers publishing on it.
high confidence · 36.5th percentile (trials denominator)
Recruiting interventional trials
From the matched ClinicalTrials.gov set
No interventional trial testing a treatment was found for this specific condition name on ClinicalTrials.gov.
See who's working on it — people publishing on this disease are often the practical next contact when no trial is listed.
Observational and natural-history studies
2 observational studies match this condition. These do not test a treatment and are not counted in the interventional-trial headline, but they are genuine research: natural-history work often defines the endpoints needed for a future rare-disease trial, and families may be able to enroll.
None of the matched observational studies is currently listed as recruiting.
Where to find support
We do not yet link condition-specific patient organisations. These umbrella groups support undiagnosed and ultra-rare families:
India — NPRD
Last verified 2026-07-26This ORPHAcode is not on our curated NPRD list (direct or Mondo-parent match). That does not decide clinical eligibility; families in India should ask a notified Centre of Excellence about current coverage.
Hand-curated for this project. ORPHAcode mappings are best-effort and may be incomplete or imprecise for umbrella categories. Parent (Mondo) matches mean the policy lists a broader category — confirm eligibility with a Centre of Excellence. Financial entitlements summarised from public policy statements and may change. This is not official government guidance.
How we counted this
Europe PMC query (preferred label + any corrected label + Orphanet and Mondo exact synonyms, stoplisted; unioned with resolved MeSH labels when available). UMLS / OMIM / NCIT cross-references are stored on the overview but are not added to the query string.
"Livedoid vasculopathy" OR "Livedo reticularis with summer ulcerations" OR "Milian atrophie blanche" OR "Segmental hyalinizing vasculitis" OR "livedoid vasculitis"
MeSH descriptor terms unioned into the query: Livedoid Vasculopathy
ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):
"Livedoid vasculopathy" OR "Livedo reticularis with summer ulcerations" OR "Milian atrophie blanche" OR "Segmental hyalinizing vasculitis" OR "livedoid vasculitis"
Study-type breakdown: 0 interventional · 2 observational · 0 expanded access. Only interventional studies enter the trial headline.
Query health: ok — strategies attempted: phrase, mesh; with hits: phrase, mesh
Run this search on ClinicalTrials.gov
Confidence reasoning
- Preferred label is multi-word and distinctive
- No synonyms dropped by stoplist
- No label/synonym collisions with other diseases in this corpus
Ingested 2026-07-27T18:15:57.022Z