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Creutzfeldt-Jakob disease presenting with bilateral hearing loss: A case report

2022-06-27 08:30SeungheeNaSeLeeJongDaeLeeEekSungLeeTaeKyeongLee
World Journal of Clinical Cases 2022年18期
關(guān)鍵詞:教科書(shū)例題背景

lNTRODUCTlON

Sporadic Creutzfeldt-Jakob disease (sCJD) is a prion disease characterized as a fatal transmissible neurodegenerative disorder[1]. The key features of sCJD are rapidly progressive dementia and diverse symptoms including myoclonus, pyramidal and extrapyramidal symptoms, cerebellar disturbance,visual symptoms, and akinetic mutism. Among them, it is known that the most commonly reported presenting symptom is cognitive decline. In other presentations, dizziness is also often the first presenting symptom of sCJD, but hearing loss as an early manifestation is very rare[2]. Herein, we report a case of acute bilateral sensorineural hearing loss as the first manifestation of sCJD.

CASE PRESENTATlON

Chief complaints

A 76-year-old man presented with bilateral sudden hearing impairment and dizziness for 10 d.

History of present illness

The hearing impairment first developed on the left side and then rapidly progressed to bilateral. He also reported dizziness that was aggravated by positional changes and accompanied by a slight gait imbalance, but he could walk without assistance.

History of past illness

He was taking medications for hypertension and diabetes for over ten years. He denied any difficulty with activities of daily living or hearing impairment before the onset of symptoms.

Personal and family history

No special history of personal and family.

Physical examination

The patient revealed no spontaneous nystagmus or gaze-evoked nystagmus. The bedside head impulse test was unremarkable. The other cranial nerves were unremarkable, and there was no limb ataxia.

Laboratory examinations

Laboratory tests including routine blood tests, autoimmune studies, thyroid function tests, and antibodies of the paraneoplastic syndrome were unremarkable except for an HbA1c of 8.1% and hyperglycemia. Pure tone audiometry (PTA) showed bilateral severe hearing impairment (Figure 1).

Imaging examinations

Given his diagnosis of sudden sensory hearing loss, the patient received corticosteroid treatment(prednisolone 60 mg/d for 10 d and tapering) but it was ineffective. Two weeks later, however, he complained of aggravated gait impairment, word-finding difficulty, disorientation, and cognitive impairment. Repeat brain MRI showed high signal intensities in the frontal, temporal, parietal, and occipital cortices on diffusion-weighted imaging (Figure 2B). Cerebrospinal fluid (CSF) analysis revealed normal concentrations of protein and glucose without pleocytosis. However, the real-time quaking-induced conversion (RT-QuIC) assay was positive, and 14-3-3 protein was detected in the CSF by western blotting.

Further diagnostic work-up

Brain magnetic resonance imaging (MRI) was within normal limits (Figure 2A).

FlNAL DlAGNOSlS

Considering all the data, we diagnosed probable sCJD. The amended diagnostic criteria added that the combination of cognitive decline, positive CSF RT-QuIC, and one or more typical CJD symptoms can draw the diagnosis of probable sCJD[3]. Because he had never undertaken neurosurgery dealing with a dura mater and the genetic analysis revealed that there was no mutation or polymorphism of the prion gene, we excluded the possibility of familial CJD or iatrogenic CJD. Moreover, our patient revealed a positive RT-QuIC test and met the criteria of probable sCJD.

《“一帶一路”沿線資源環(huán)境與社會(huì)發(fā)展特征分析》采用信息融合和數(shù)據(jù)挖掘的方法對(duì)“一帶一路”沿線國(guó)家和區(qū)域的人文和自然等多源數(shù)據(jù)進(jìn)行處理,對(duì)“一帶一路”沿線國(guó)家和地區(qū)的資源環(huán)境與社會(huì)發(fā)展特征進(jìn)行了全面細(xì)致的分析.該書(shū)夯實(shí)了該方面的數(shù)據(jù)和信息基礎(chǔ),同時(shí)為“一帶一路”相關(guān)科學(xué)研究提供支撐.但是,“一帶一路”倡議的實(shí)施是一個(gè)長(zhǎng)期的過(guò)程,數(shù)據(jù)是基礎(chǔ),但還需要完備的政策指導(dǎo)和合理的規(guī)劃設(shè)計(jì),更依賴于自下而上的有效參與.單純的數(shù)據(jù)并不能高效的支撐“一帶一路”倡議的實(shí)施工作,接下來(lái)應(yīng)基于多源數(shù)據(jù),集成數(shù)據(jù)庫(kù),建立地理信息服務(wù)平臺(tái),以便可以更高效快速的為“一帶一路”相關(guān)工作的實(shí)施提供服務(wù).

TREATMENT

Because of the characteristics of sCJD, the intractable rapidly progressive dementia[1], he received conservative care.

The patient’s symptoms rapidly progressed into akinetic mutism within only two months after the onset of bilateral hearing impairment.

OUTCOME AND FOLLOW-UP

整體來(lái)看,RJ版教科書(shū)與CM教科書(shū)有理數(shù)章節(jié)的例題素材選取具有一定的共性,即均是無(wú)背景的例題所占比重大,且無(wú)背景的例題均是有理數(shù)加減乘除運(yùn)算等類的題目.另外,兩版教科書(shū)有背景的例題中,均有一小部分例題只是為了有背景”而創(chuàng)設(shè)背景,例題的背景素材無(wú)實(shí)際意義.

DlSCUSSlON

G組患兒家屬的滿意度為97.87%,明顯高于D組的85.1%,兩組相比,差異有統(tǒng)計(jì)學(xué)意義(P<0.05)。見(jiàn)表3。

Hearing impairment as an early symptom of sCJD has been described in a few reports[5,6]. Those patients were elderly, older than 65 years, and first complained of only suddenly developed bilateral hearing impairment and subjective unsteadiness. Our patient’s hearing loss were also bilateral and unresponsive to steroid treatment. Postmortem studies in sCJD have revealed that the prion protein deposition in the brainstem is symmetrical and starts in the early stage of sCJD[7]. These neuropathologic characteristics account for the bilaterality of the hearing impairment in patients with sCJD.

The authors of a previous report conducted a brain MRI at the initial presentation, and it was within normal limit[5]. Our patient showed imaging findings that reflected his complaints and symptoms of sCJD. At his first visit when he complained of only hearing impairment and vague dizziness, the brain MRI was unremarkable. After other symptoms developed, however, repeat brain MRI revealed characteristic high signal intensities of the bilateral cerebral cortices, which were a clue for the diagnosis of sCJD.

This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BYNC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is noncommercial. See: https://creativecommons.org/Licenses/by-nc/4.0/

他說(shuō):“你換購(gòu)到機(jī)票沒(méi)有?我是第一次賣(mài)里程呢,做一下售后調(diào)查,不知道會(huì)不會(huì)有什么問(wèn)題?!绷A;卮穑骸皼](méi)有問(wèn)題,我已經(jīng)在云南騰沖。”

CONCLUSlON

The patient presented with sudden onset hearing impairment and dizziness, followed by progressive cognitive impairment and confusion. Repeat brain MRI revealed characteristic findings of sCJD, and the RT-QuIC test was positive. For patients with abrupt bilateral hearing impairment, especially in the elderly, various differential diagnoses, including sCJD, should be considered. Moreover, when sCJD is suspected, close follow-up with thorough history taking and neurologic examinations and repeated workups that include brain diffusion-weighted imaging and CSF analysis will be helpful.

This patient presented with an abrupt onset of bilateral hearing impairment and dizziness as the first manifestation of sCJD. Although he only complained of otologic symptoms and was diagnosed initially with bilateral sensorineural hearing loss, the patient then developed additional neurologic symptoms including cognitive decline and prominent gait imbalance, which rapidly progressed. The amended diagnostic criteria of sCJD area that the combination of positive CSF RT-QuIC and progressive cognitive impairment or any of typical CJD symptoms can draw the diagnosis of probable sCJD[3]. Our patient revealed a positive RT-QuIC test and met the criteria of probable sCJD. The possibilities of familial or iatrogenic CJD were excluded because there was no mutation or polymorphism of the prion gene and he had no history of epidemiological evidence. Although the etiology of sCJD has been unknown, many researchers assumed that the prion disease might be initiated by the stochastic misfolded cellular prion protein or mutations in the prion protein gene at ongoing neurogenesis areas[4].

FOOTNOTES

Lee ES conceived and designed the study; Lee TK provided supervision; Lee ES and Lee collected the data; Lee SN wrote the first draft of the manuscript; Lee SA and Lee JD edited and contributed to critical revision; and All authors read and approved the final version of the manuscript for submission.

National Research Foundation of Korea, No. 2019R1C1C1006539.

在此基礎(chǔ)上初步設(shè)計(jì)出幾套不同風(fēng)格的界面用于備選。同時(shí)要做到以下幾點(diǎn):①把用戶想象成計(jì)算機(jī)初學(xué)者;②盡量用易于識(shí)別的圖示表達(dá),少用文字;③能夠用鼠標(biāo)點(diǎn)選的絕不做成填寫(xiě);④讓用戶感覺(jué)不到技術(shù)的存在;⑤做到一個(gè)沒(méi)有“幫助”的軟件。

The authors declare that this single case report has been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki.

The authors declare that they have no conflict of interest.

The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).

“中央空調(diào)主機(jī)智能節(jié)電管理系統(tǒng)”是通過(guò)采集末端和室外的溫、濕度變化信號(hào),經(jīng)過(guò)服務(wù)器AS4N分析和運(yùn)算,給出控制信號(hào)到控制器GCRE,控制器控制主機(jī)按原廠自有的邏輯調(diào)節(jié)空調(diào)負(fù)載。把空調(diào)主機(jī)和末端直接、統(tǒng)一管理,實(shí)現(xiàn)了中央空調(diào)系統(tǒng)的協(xié)調(diào)、即時(shí)運(yùn)行和綜合性能優(yōu)化。智能節(jié)電管理系統(tǒng)的核心就是數(shù)據(jù)庫(kù)和策略庫(kù)。如圖3所示。

Among the presenting symptoms of our patient, the dizziness was nonspecific and vague, but the hearing impairment was abrupt and very severe. Furthermore, the hearing difficulty was broad, from low to high frequency. When a patient with cognitive decline is suspected of having hearing difficulty,an appropriate evaluation is difficult because laboratory tests, such as pure tone audiometry, cannot be obtained without patient cooperation, and an accurate history of onset time and the pattern of the hearing impairment is needed. In sCJD, the most common presenting symptom is cognitive decline[3].Thus, even if hearing impairment occurs in the early stage of sCJD, evaluations for the presence of hearing symptoms and otologic function under rapidly progressive cognitive decline are difficult. In our patient, however, the history of hearing impairment and the result of PTA were reliable because the patient did not complain of cognitive impairment at presentation.

3.大數(shù)據(jù)管理決策能力。 “互聯(lián)網(wǎng)+”時(shí)代,政府治理主體和對(duì)象數(shù)據(jù)信息呈爆發(fā)式增長(zhǎng),局限于傳統(tǒng)的監(jiān)測(cè)、管理、應(yīng)對(duì)手段無(wú)法摸清經(jīng)濟(jì)社會(huì)發(fā)展及政府行政真實(shí)情況,更難做出科學(xué)有效的治理決策,只有借助大數(shù)據(jù)技術(shù)獲取、處理和分析海量信息,支撐經(jīng)濟(jì)管理、政務(wù)服務(wù)和社會(huì)關(guān)系塑造等治理活動(dòng),才能夠保障政府行為的精確度和科學(xué)性。

South Korea

Seunghee Na 0000-0001-8578-8578; Se A Lee 0000-0002-6263-1903; Jong Dae Lee 0000-0003-2866-9841;Eek-Sung Lee 0000-0003-3517-8207; Tae-Kyeong Lee 0000-0001-6913-4689.

Korean Neurological Association.

Ma YJ

A

在農(nóng)業(yè)解決方案中,頗具前景的是創(chuàng)新型數(shù)字農(nóng)業(yè)業(yè)務(wù),能夠通過(guò)數(shù)字技術(shù)帶來(lái)最佳用戶體驗(yàn)并增加效率。數(shù)字技術(shù)的應(yīng)用在每個(gè)地區(qū)的需求不一樣,數(shù)字農(nóng)業(yè)平臺(tái)涉及的氣候數(shù)據(jù)采集、病害診斷、解決方法推薦等,將會(huì)幫助農(nóng)戶更好種植,逐步達(dá)到可持續(xù)農(nóng)業(yè)發(fā)展的愿景。

(2)對(duì)于識(shí)別樣本,若不滿足式(13)條件則說(shuō)明高壓開(kāi)關(guān)柜為異常狀態(tài)。此時(shí),計(jì)算R幀語(yǔ)料的特征和其關(guān)于所有訓(xùn)練模型的似然值p(X/GMMn)。

Ma YJ

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