Laboratory Investigations for Diagnosing Linear Morphea
Laboratory investigations can support the diagnosis of linear morphea, with antinuclear antibodies (ANA) being the most valuable blood test, found in approximately 57% of patients with morphea. 1
Key Laboratory Investigations
Antinuclear antibodies (ANA) are detected in a high rate of morphea cases (approximately 57% of patients) and should be the primary laboratory test when suspecting linear morphea 1
Scleroderma-related autoantibodies can be found in approximately 52.4% of morphea patients using line-blot testing, with anti-TRIM21/Ro52 antibodies being the most frequently detected (36.4% of antibody-positive cases) 1
Skin biopsy from the most active sclerotic area is recommended by the British Association of Dermatologists when there is diagnostic uncertainty, atypical features, or features mimicking other conditions 2
Anti-histone antibodies and rheumatoid factor are commonly detected in morphea cases and should be included in the laboratory workup 1
Anti-DNA and anti-nucleosome antibodies are typically negative in morphea patients, which can help differentiate from other autoimmune conditions 1
Laboratory Findings to Rule Out Other Conditions
Complete blood count may reveal eosinophilia in some cases, particularly when there is associated eosinophilic fasciitis, which is considered part of the severe end of the morphea spectrum 3
Inflammatory markers such as erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) may be elevated during the active inflammatory phase of linear morphea 3
Absence of sclerodactyly-specific antibodies helps differentiate morphea from systemic sclerosis, as morphea patients typically lack anti-Scl-70 and anti-centromere antibodies 3
Diagnostic Algorithm for Linear Morphea
Initial laboratory screening:
Advanced antibody testing:
Histopathological confirmation:
Clinical Pearls and Pitfalls
Positive ANA does not confirm the diagnosis but supports it when clinical features are consistent with linear morphea 1
Negative laboratory findings do not exclude the diagnosis if clinical presentation is typical for linear morphea 3
Monitoring disease activity is challenging and should include both clinical assessment using the Localized Scleroderma Cutaneous Assessment Tool (LoSCAT) and laboratory parameters 2
Differentiate from lichen sclerosus which can sometimes mimic morphea, especially in extragenital sites 4
Consider full workup for associated autoimmune conditions as patients with morphea may have concurrent autoimmune disorders 3