Primary amyloidosis with dry eyes and dry mouth--a case report.

T Itoh, S Ohashi, T Tsujino, M Takenaka, H Kodama, M Kishihara, T Inatome, T Inoh
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引用次数: 8

Abstract

We report a rare case of dry eyes and dry mouth caused by primary amyloidosis. A 66-year-old woman with keratoconjunctivitis sicca and xerostomia died of acute respiratory failure. Shirmer's test, gum test, and sialography indicated Sjögren's syndrome. Lip biopsy revealed amyloid deposition around the salivary ducts. Bence-Jones protein was noted in the urine. At autopsy, amyloid deposition was identified histochemically in many organs, mainly on the vessel walls. Primary amyloidosis should be considered as a differential diagnosis of Sjögren's syndrome.

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原发性淀粉样变性伴眼口干涩1例报告。
我们报告一例罕见的由原发性淀粉样变引起的眼干和口干。一位66岁的妇女,患有干燥性角膜结膜炎和口干症,死于急性呼吸衰竭。雪默氏试验,牙龈试验和唾液造影显示Sjögren综合征。唇活检显示唾液管周围淀粉样蛋白沉积。尿液中检测到本斯-琼斯蛋白。尸检发现,淀粉样蛋白沉积在许多器官中,主要是在血管壁上。原发性淀粉样变应被视为Sjögren综合征的鉴别诊断。
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