Tiller-Borcich J K, Urich H
J Neurol Neurosurg Psychiatry. 1986 May;49(5):581-4. doi: 10.1136/jnnp.49.5.581.
A case is presented of the ataxic variety of Creutzfeldt-Jakob disease with particular reference to the cerebellar cortex. The main features were loss of granule cells, subtotal in the vermis, severe in the lateral lobes, mild to moderate loss of Purkinje cells and preservation of tangential and basket fibres. The Purkinje cell dendrites showed malorientation and hypertrophy of the primary and secondary branches, the so-called "antler" or "staghorn" deformity. These findings indicate that remodelling of the dendritic tree may start early in the course of the disease even in adults, the total length of history in this case being eight months. They do not throw any additional light on the pathogenesis of the dendritic abnormalities, in particular on the controversy whether they are a non-specific response of the Purkinje cell to a variety of noxious agents or a reaction to partial deafferentation. The authors favour the latter hypothesis.
本文报告1例具有共济失调症状的克雅氏病,特别提及小脑皮质的情况。主要特征为颗粒细胞缺失,蚓部缺失程度为部分性,外侧叶严重缺失,浦肯野细胞有轻度至中度缺失,切向纤维和篮状纤维保留。浦肯野细胞树突出现初级和次级分支排列紊乱及肥大,即所谓的“鹿角”或“鹿角状”畸形。这些发现表明,即使在成年人中,树突重塑可能在疾病过程早期就已开始,该病例的总病程为8个月。它们并未为树突异常的发病机制提供更多线索,特别是关于它们是浦肯野细胞对多种有害因子的非特异性反应还是对部分传入神经阻滞的反应这一争议。作者支持后一种假说。