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A case of isolated amyloidosis in extraocular muscle mimicking thyroid eye disease
YuePing Li1, Yuchuan Wang1, Wei Zhang1
1Pediatric Ophthalmology and Strabismus Department, Tianjin Eye Hospital; Clinical College of Ophthalmology of Tianjin Medical University; Tianjin Key Laboratory of Ophthalmology and Vision Science, Tianjin, China.
Abstract:
A 24-year-old woman presented with periorbital pain, progressive diplopia, and restricted eye movement. Routine blood testing was normal except for increased levels of thyroid peroxidase autoantibody (TPOAb) and thyroglobulin autoantibody (TGAb). Orbital computed tomography revealed fusiform thickening of the rectus muscles belly, with tendon sparing, as in thyroid eye disease. Rectus muscle biopsy revealed isolated amyloidosis. Further workup showed no evidence of systemic amyloidosis.
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