Department of Pathology, Massachusetts General Hospital, Harvard University, Boston, 02114-2696, USA.
Acta Neuropathol. 2010 Nov;120(5):683-8. doi: 10.1007/s00401-010-0745-3. Epub 2010 Sep 14.
Among more than 2,050 brains in our Alzheimer disease brain banks, we came across three brains with well-demarcated indurated white-yellow nodules in the amygdalas. Microscopically, these nodules were composed of numerous lipid-laden macrophages located in the central region surrounded by an eosinophilic hyaline-like material with minimal reactive gliosis in the periphery. Neurons within these lesions had a normal appearance but were moderately decreased in number. Beta-amyloid, tau and alpha-synuclein immunostaining revealed no abnormal deposits within the nodules. The three patients had long histories of dementia (one linked to a presenilin-1 mutation). The neuropathological diagnoses were Alzheimer disease in two of them and an unclassified tauopathy with argyrophilic grains in the third. In conclusion, the pathogenesis of these lesions is uncertain. We favor that the degeneration has some relationship to the underlying dementing disease, either secondary to deafferentation or an alteration in metabolic demand, perhaps related to the bi-directional anatomical and functional connections that exist between the amygdala and the hippocampus or less likely as a primary event.
在我们的阿尔茨海默病脑库中超过 2050 个大脑中,我们发现三个大脑的杏仁核中有边界清楚的硬结性黄白色结节。显微镜下,这些结节由许多富含脂质的巨噬细胞组成,位于中央区域,周围环绕着嗜酸性玻璃样物质,周边反应性神经胶质增生最小。这些病变内的神经元外观正常,但数量中度减少。β-淀粉样蛋白、tau 和 alpha-synuclein 免疫染色显示结节内无异常沉积物。这三个患者都有长期的痴呆病史(一个与早老素-1 突变有关)。神经病理学诊断为其中两人的阿尔茨海默病,第三人为未分类的 tau 病伴银染颗粒。总之,这些病变的发病机制尚不确定。我们认为这种退化与潜在的痴呆疾病有关,可能是继发于去传入或代谢需求的改变,可能与杏仁核和海马体之间存在的双向解剖和功能连接有关,或者不太可能是原发性事件。