Nehen J H
Acta Ophthalmol (Copenh). 1979 Apr;57(2):287-95. doi: 10.1111/j.1755-3768.1979.tb00493.x.
The present paper reports a case of primary localized amyloid tumour of the orbit in a 68-year-old woman in whom myasthenia gravis had been diagnosed 33 years before. An amyloid tumour with this location is very rare, and up to the present time only 13 cases have been recorded in the literature. The reported orbital amyloid tumour revealed a considerable accumulation of activity at orbital scintigraphy with 99Tc(m) and, compared with the conventional pseudotumours, a distinct rise in density at computed tomography after intravenous infusion of iodized contrast medium.
本文报告了一例68岁女性眼眶原发性局限性淀粉样瘤病例,该患者33年前被诊断为重症肌无力。眼眶处发生的淀粉样瘤非常罕见,截至目前,文献中仅记载了13例。报告的眼眶淀粉样瘤在99Tc(m)眼眶闪烁扫描中显示有大量放射性聚集,与传统的假瘤相比,静脉注射碘化造影剂后在计算机断层扫描中密度明显升高。