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A form of dermatomyositis characterized by the presence of typical skin finding swithout muscle weakness. Some of the skin changes that suggest dermatomyositis include a pink rash on the face, neck, forearms and upper chest; Gottron's papules and heliotrope eyelids. Pruritis and photosensitivity are common, as is scalp inflammation and thinning of the hair.While patients with amyopathic dermatomyositis should not have clinically evident muscle weakness, minor muscle abnormalities may be included.Fatigue is reported in at least 50% of patients. Some cases have beenassociated with internal malignancy and/or interstitial lung disease. Treatment may include sun avoidance, ample use of sunscreen, topical corticosteroids, antimalarial agents, methotrexate, mycophenolate mofetil, or intravenous (IV) immunoglobulin.
Biomarker and diagnostic research for amyopathic dermatomyositis has been reported in the published literature.
1 clinical trial registered, 1 recruiting. Interventions under study include drug therapy. Pipeline includes 1 PHASE2. Research is primarily sponsored by academic and government institutions.
108 publications have been identified in PubMed for amyopathic dermatomyositis. Research spans Case Report / Case Series (50%), Review / Meta-Analysis (16%), and Epidemiology / Natural History (14%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 54 |
Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 1:53 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Research summaries | 17 | 16% |
Disease patterns and progression | 15 | 14% |
Other research | 11 | 10% |
Testing and diagnosis research | 7 | 6% |
Laboratory research | 2 | 2% |
Clinical study results | 1 | 1% |
New treatment approaches | 1 | 1% |
Dutsch-Wicherek M (2026). [PMID: 42194620](https://pubmed.ncbi.nlm.nih.gov/42194620/). *J Clin Med*. [Review / Meta-Analysis]
Regan M (2026). [PMID: 41881481](https://pubmed.ncbi.nlm.nih.gov/41881481/). *BMJ Case Rep*. [Case Report / Case Series]
Wang Y (2026). [PMID: 41537529](https://pubmed.ncbi.nlm.nih.gov/41537529/). *Clin Exp Rheumatol*. [Epidemiology / Natural History]
He K (2026). [PMID: 41239078](https://pubmed.ncbi.nlm.nih.gov/41239078/). *Clin Rheumatol*. [Diagnostic / Biomarker]
Zhang H (2026). [PMID: 41520886](https://pubmed.ncbi.nlm.nih.gov/41520886/). *J Am Acad Dermatol*. [Other]
Sandhu A (2026). [PMID: 41768519](https://pubmed.ncbi.nlm.nih.gov/41768519/). *Arch Intern Med Res*. [Diagnostic / Biomarker]
Horiot V (2026). [PMID: 42134019](https://pubmed.ncbi.nlm.nih.gov/42134019/). *Ann Dermatol Venereol*. [Other]
Sakai A (2026). [PMID: 42003326](https://pubmed.ncbi.nlm.nih.gov/42003326/). *J Dermatol*. [Other]
Kutwin M (2026). [PMID: 42074677](https://pubmed.ncbi.nlm.nih.gov/42074677/). *J Clin Med*. [Review / Meta-Analysis]
Pillai P (2026). [PMID: 41877413](https://pubmed.ncbi.nlm.nih.gov/41877413/). *Singapore Med J*. [Diagnostic / Biomarker]
AI-curated news mentioning amyopathic dermatomyositis
Updated Sep 13, 2026
A recent study highlights the diagnostic potential of interferon-stimulated gene 15 (ISG15) muscle expression in dermatomyositis. This research could enhance diagnostic accuracy for this rare autoimmune disease.
Orsini will serve as the specialty pharmacy partner for Priovant's LISRAYA™ (brepocitinib), enhancing patient access to this innovative treatment. The drug was evaluated in the VALOR study, the largest placebo-controlled trial for dermatomyositis, indicating significant advancements in rare disease therapies.
Priovant Therapeutics secures FDA approval for its dual TYK2/JAK1 inhibitor, marking a significant milestone as the first approved treatment for adult dermatomyositis (DM). The approval is supported by data from the largest DM study ever conducted, the Valor trial, allowing use without restrictions based on disease activity or previous treatments.
A case study highlights the recovery of a patient with fulminant anti-nuclear matrix protein 2 antibody-positive dermatomyositis, characterized by massive anasarca and respiratory failure, after prolonged immunosuppression and rehabilitation. This research underscores the potential for recovery in severe cases of this rare autoimmune disease.
A recent case report details a pediatric patient with AQP4+ neuromyelitis optica spectrum disorder (NMOSD), MDA5+ clinically amyopathic dermatomyositis, and secondary hemophagocytic lymphohistiocytosis (sHLH). This study contributes to the understanding of these rare conditions and their clinical presentations.