| Literature DB >> 26421831 |
Yuichi Hayashi1, Yasushi Iwasaki2, Nobuaki Yoshikura3, Takahiko Asano4, Taku Hatano5, Shinsui Tatsumi2, Katsuya Satoh6, Akio Kimura3, Tetsuyuki Kitamoto7, Mari Yoshida2, Takashi Inuzuka3.
Abstract
We report a case of autopsy-verified MM2-thalamic-type sporadic Creutzfeldt-Jakob disease (sCJD) in a 46-year-old patient with a 16-month history of abnormal behavior, progressive dementia, insomnia, and speech disturbances without family history. Neurological examination revealed progressive dementia, frontal signs, insomnia, speech disturbance, gait disturbance and bilaterally exaggerated tendon reflexes. Both brain MRI and cerebrospinal fluid examinations, including 14-3-3 protein, yielded normal results. An easy Z-score (eZIS) analysis for (99m)Tc-ethyl cysteinate dimer-single photon emission computed tomography ((99m)Tc-ECD-SPECT) revealed decreased regional cerebral blood flow in the bilateral thalami and medulla oblongata. PRNP gene analysis revealed methionine homozygosity at codon 129 without mutation. Neuropathological examinations revealed severe neuronal loss, gliosis, and hypertrophic astrocytosis in the medial thalamus and inferior olivary nucleus. A slight depletion of Purkinje cells was observed. PrP immunostaining showed no obvious PrP deposits in the basal ganglia, thalamus, cerebellum, or brainstem; however, mild synaptic-type PrP deposits with some smaller plaque-like structures were only partially observed in the localized region of the frontal lobe with the spongiform change. Western blot analyses of protease-resistant PrP showed a type 2 pattern. In conclusion, eZIS analysis of (99m)Tc-ECD-SPECT images is useful for detecting both thalamic and medullary lesions. This is the first case of medullary lesions detected in a live patient with MM2-thalamic-type sCJD using SPECT.Entities:
Keywords: ECD-SPECT; Easy Z-score analysis; MM2-thalamic-type; Medulla oblongata lesion; Sporadic Creutzfeldt–Jakob disease
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Year: 2015 PMID: 26421831 DOI: 10.1016/j.jns.2015.09.356
Source DB: PubMed Journal: J Neurol Sci ISSN: 0022-510X Impact factor: 3.181