Why the study?
Acute lupus myocarditis and pulmonary arterial hypertension are rare complications of SLE, and no previous reports had shown their coexistence.
Concurrent acute lupus myocarditis, PAH, and digital gangrene can occur as an initial manifestation of SLE and may be successfully managed with immunosuppression, anticoagulation, and catheter-directed thrombolysis.
May support early intensive immunosuppression in this rare overlap; leaves open generalizability and a possible unifying vasculitic mechanism.
Acute lupus myocarditis and pulmonary arterial hypertension (PAH) are rare complications associated with systemic lupus erythematosus (SLE). No previous reports have shown the coexistence of these disorders. Here we present a 41-year-old patient with SLE who concurrently developed severe acute lupus myocarditis and PAH with digital gangrene as an initial manifestation. Acute lupus myocarditis and PAH were successfully treated with prednisolone and intravenous cyclophosphamide pulse therapy (600-700 mg × 6) along with anticoagulant therapy. Catheter-directed thrombolysis was required for digital gangrene caused by vasculitis. Concurrent development of these rare disorders may represent a common mechanism such vasculitis as an underlining cause of SLE.
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Ando et al. (2019) studied this question.
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