AnaPath Services GmbH, Liestal, Switzerland.
Department of Veterinary Clinical Medicine, University of Illinois, Urbana, Illinois, USA.
J Vet Intern Med. 2024 May-Jun;38(3):1730-1736. doi: 10.1111/jvim.17055. Epub 2024 Mar 27.
Two 9-week-old female littermate German Shepherd puppies showed severe high-frequency low-amplitude trembling that worsened with movement. The white matter (WM) of the central nervous system (CNS) showed bilateral diffuse severe spongiosis in the cerebellum, brainstem, spinal cord, and the neuropil of the oculomotor and red nuclei. The cortical corona radiata was less severely affected. Rare necrotic or apoptotic glia-like cells also were identified in the WM. Luxol fast blue staining disclosed severe diffuse myelin loss in the entire CNS; peripheral nerves were spared. Glial fibrillary acidic protein immunohistochemistry showed diffuse astrogliosis and astrocytosis in the WM. Genetic analyses of the littermates excluded the aspartoacylase (ASPA) gene as a candidate for this condition in dogs. In conclusion, this description of a rare congenital spongiform leukodystrophy in the German Shepherd breed, closely resembling to Canavan disease in humans, is likely caused by a genetic alteration unrelated to the ASPA gene.
两只 9 周龄的雌性同窝德国牧羊犬幼犬出现严重的高频低幅度震颤,且随运动而加重。中枢神经系统(CNS)的白质(WM)在小脑、脑干、脊髓和动眼神经及红核的神经毡中显示双侧弥漫性严重海绵状变性。皮质冠状辐射区受影响较轻。WM 中还罕见地发现坏死或凋亡的胶质样细胞。卢索快速蓝染色显示整个 CNS 有严重弥漫性髓鞘丢失;周围神经未受累。胶质纤维酸性蛋白免疫组化显示 WM 中有弥漫性星形胶质增生和星形胶质细胞增多。对同窝犬的基因分析排除了天冬氨酸酶(ASPA)基因作为该疾病的候选基因。总之,这种在德国牧羊犬品种中罕见的先天性海绵状白质营养不良的描述与人类的 Canavan 病非常相似,可能是由与 ASPA 基因无关的遗传改变引起的。