Maruyama K, Ikeda S, Yanagisawa N, Nakazato M
Department of Medicine (Neurology), Shinshu University School of Medicine, Matsumoto, Japan.
J Neurol Sci. 1987 Oct;81(1):11-8. doi: 10.1016/0022-510x(87)90180-8.
To confirm amyloid deposition we performed aspiration biopsy of abdominal fat tissue in 14 patients with type I familial amyloid polyneuropathy (FAP). All patients, about half of whom were at an early stage of disease and lacking severe neurological disabilities, showed positive amyloid deposition in preparations stained with Congo red. On light and electron microscopic examinations deposits of amyloid were observed around fat cells and small vascular walls, and among collagen bundles. All patients in the study were demonstrated to have a variant transthyretin in their sera by radioimmunoassay. Abdominal fat tissue aspiration can be easily performed with an ordinary syringe and is very sensitive for detecting amyloid deposition. The procedure is valuable in the diagnosis of type I FAP patients with actual deposition of amyloid substance, even at an early stage.
为了确认淀粉样蛋白沉积,我们对14例I型家族性淀粉样多神经病(FAP)患者进行了腹部脂肪组织穿刺活检。所有患者中约一半处于疾病早期且无严重神经功能障碍,在刚果红染色的标本中均显示淀粉样蛋白沉积阳性。在光镜和电镜检查中,可见脂肪细胞和小血管壁周围以及胶原束之间有淀粉样蛋白沉积。通过放射免疫测定法证实,研究中的所有患者血清中均有一种变异的转甲状腺素蛋白。腹部脂肪组织穿刺活检用普通注射器即可轻松完成,对检测淀粉样蛋白沉积非常敏感。该方法对于诊断有淀粉样物质实际沉积的I型FAP患者很有价值,即使在疾病早期也是如此。