Kyle R A, Gertz M A, Linke R P
Division of Hematology and Internal Medicine, Mayo Clinic, Rochester, Minnesota 55905.
Am J Clin Pathol. 1992 Feb;97(2):250-3. doi: 10.1093/ajcp/97.2.250.
Thirty-five patients seen at the Mayo Clinic from 1968 to 1977 who had carpal tunnel syndrome and local deposition of amyloid without evidence of systemic amyloidosis were identified. The unlabeled immunoperoxidase method was used with antisera against purified amyloid proteins of the AA, A kappa, A lambda, AF/ASC1 (prealbumin) (transthyretin), and AB (beta 2-microglobulin) types. In 33 of the 35 patients, amyloid stained with antisera to transthyretin; in the remaining 2 patients, the amyloid did not stain with any antisera. Nine of the 35 patients had a monoclonal protein in the serum, and 2 had a monoclonal light chain in the urine. Systemic amyloidosis or multiple myeloma did not develop in any of these 11 patients. During follow-up, systemic amyloidosis developed in only 2 of the 35 patients: 1 had senile systemic amyloidosis and 1 had tissue that was inadequate for immunohistochemical staining. Amyloid localized to the tenosynovium consists of transthyretin, and systemic amyloidosis rarely develops.
我们确定了1968年至1977年期间在梅奥诊所就诊的35例患有腕管综合征且有淀粉样蛋白局部沉积但无系统性淀粉样变性证据的患者。采用未标记免疫过氧化物酶法,使用针对AA、Aκ、Aλ、AF/ASC1(前白蛋白)(转甲状腺素蛋白)和AB(β2微球蛋白)型纯化淀粉样蛋白的抗血清。35例患者中有33例的淀粉样蛋白用转甲状腺素蛋白抗血清染色;其余2例患者的淀粉样蛋白未被任何抗血清染色。35例患者中有9例血清中有单克隆蛋白,2例尿中有单克隆轻链。这11例患者中均未发生系统性淀粉样变性或多发性骨髓瘤。在随访期间,35例患者中仅2例发生了系统性淀粉样变性:1例为老年性系统性淀粉样变性,1例的组织不适合进行免疫组织化学染色。定位于腱鞘的淀粉样蛋白由转甲状腺素蛋白组成,系统性淀粉样变性很少发生。