Department of Neuropathology, Kyushu University, Fukuoka, Japan.
Department of Neurology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
Neuropathology. 2021 Apr;41(2):152-158. doi: 10.1111/neup.12717. Epub 2021 Feb 4.
We report the general autopsy findings of abnormal prion protein (PrP) deposits with their seeding activities, as assessed by the real-time quaking-induced conversion (RT-QuIC) method, in a 72-year-old female patient with sporadic Creutzfeldt-Jakob disease (sCJD). At 68 years of age, she presented with gait disturbance and visual disorders. Electroencephalography showed periodic synchronous discharge. Myoclonus was also observed. A genetic test revealed that PRNP codon 129 was methionine/methionine (MM). She died of pneumonia three years and four months after disease onset, and a general autopsy was performed. The brain weighed 650 g and appeared markedly atrophic. Immunohistochemistry for PrP revealed synaptic PrP deposits and coarse PrP deposits in the cerebral cortices, basal ganglia, cerebellum, and brainstem. Western blot analysis identified type 1 proteinase-K-resistant PrP in frontal cortex samples. PrP deposits were also observed in systemic organs, including the femoral nerve, psoas major muscle, abdominal skin, adrenal medulla, zona reticularis of the adrenal gland, islet cells of the pancreas, and thyroid gland. The RT-QuIC method revealed positive seeding activities in all examined organs, including the frontal cortex, femoral nerve, psoas major muscle, scalp, abdominal skin, adrenal gland, pancreas, and thyroid gland. The following 50% seeding dose (SD ) values were 9.5 (frontal cortex); 8 ± 0.53 (femoral nerve); 7 ± 0.53 (psoas major muscle); and 7.88 ± 0.17 (scalp). The SD values for the adrenal gland, dermis, pancreas, and thyroid gland were 6.12 ± 0.53, 5.25, 4.75, and 4.5, respectively. PrP deposits in general organs may be associated with long-term disease duration. This case indicated the necessity for general autopsies in sCJD cases to establish strict infection control procedures for surgical treatment and to examine certain organs.
我们报告了一例散发性克雅氏病(sCJD)患者的一般尸检发现,该患者异常朊病毒蛋白(PrP)沉积及其种籽活性可通过实时震颤诱导转化(RT-QuIC)方法来评估。患者为 72 岁女性,发病时表现为步态障碍和视觉障碍。脑电图显示周期性同步放电。阵挛性肌阵挛也被观察到。基因检测显示 PRNP 密码子 129 为蛋氨酸/蛋氨酸(MM)。发病后 3 年零 4 个月,患者因肺炎死亡,并进行了全面尸检。大脑重 650 克,明显萎缩。PrP 的免疫组织化学显示皮质、基底节、小脑和脑干存在突触 PrP 沉积和粗糙 PrP 沉积。Western blot 分析显示额皮质样本中存在 1 型蛋白酶 K 抗性 PrP。系统器官中也观察到 PrP 沉积,包括股神经、腰大肌、腹部皮肤、肾上腺髓质、肾上腺网状带、胰岛细胞和甲状腺。RT-QuIC 方法显示所有检查器官(包括额皮质、股神经、腰大肌、头皮、腹部皮肤、肾上腺、胰腺和甲状腺)均具有阳性种籽活性。50%种籽剂量(SD)值如下:额皮质为 9.5;股神经为 8±0.53;腰大肌为 7±0.53;头皮为 7.88±0.17。肾上腺、真皮、胰腺和甲状腺的 SD 值分别为 6.12±0.53、5.25、4.75 和 4.5。一般器官中的 PrP 沉积可能与疾病持续时间较长有关。该病例表明,sCJD 病例需要进行全面尸检,以建立严格的感染控制程序用于手术治疗,并检查某些器官。