Abstract
The overlapping nature of autoimmune diseases makes diagnosing and stratifying prognosis
extremely difficult. Scleromyositis, the most common overlap syndrome, is typically
seen in adults and is rarely seen in children. An overlap syndrome like scleromyositis
would have clinical features of at least two connective tissue diseases (juvenile
dermatomyositis and systemic sclerosis). Furthermore, the presence of anti-PM/Scl
antibodies is critical. We describe a patient who presented with widespread skin tightening,
hoarseness of voice, dysphagia, and muscle weakness that had been present for 6 months.
The patient was diagnosed with overlap juvenile scleromyositis (scleroderma-dermatomyositis
overlap). In practice, distinguishing this syndrome from dermatomyositis and scleroderma
is critical.
Keywords
juvenile dermatomyositis - diffuse systemic sclerosis - scleroderma - Raynaud's phenomenon
- connective tissue disease - overlap syndrome - scleromyositis - interstitial lung
disease