Amitouj S Sidhu, Charles E L Walker, Thomas D Riisfeldt, Peter J Tweedie, Natasha Gerbis, Emily J Sutherland, Neil G Simon, Lucy K Somerville, Ross Bradbury, Raymond Cook, Jonathon Parkinson, Robert Goetti, Ian C Francis
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While <i>Streptococcus pneumoniae</i> is well recognised to cause bacterial meningitis, direct extension into the central nervous system parenchyma is rare.</p><p><strong>Case presentation: </strong>A previously well 49-year-old man presented with sudden onset severe headache, fevers, neck stiffness, and reduced consciousness. The manifestations of SME in this patient were bilateral pupil-involving third-nerve palsies, wall-eyed bilateral internuclear ophthalmoplegia (WEBINO), bilateral blindness, bilateral deafness, a right lower motor neuron facial palsy, and upper motor neuron signs in his limbs. Initially, a partial response to high dose intravenous antibiotics occurred, but with administration of intravenous corticosteroids, further substantial resolution of the patient's neurological and neuro-ophthalmological deficits occurred.</p><p><strong>Conclusion: </strong>This case highlights the benefit of multidisciplinary diagnostic and therapeutic interventions in a case of SME complicated by bilateral pupil-involving third-nerve palsies, WEBINO, bilateral blindness, bilateral deafness, a right lower motor neuron facial palsy, and upper motor neuron signs. It appears to be the first reported case of SME with this rare collection of neuro-ophthalmological abnormalities.</p>","PeriodicalId":9635,"journal":{"name":"Case Reports in Ophthalmology","volume":"15 1","pages":"423-429"},"PeriodicalIF":0.5000,"publicationDate":"2024-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11078538/pdf/","citationCount":"0","resultStr":"{\"title\":\"Successful Management of Acute Streptococcal Meningoencephalitis Complicated by Bilateral Third-Nerve Palsies, Wall-Eyed Bilateral Internuclear Ophthalmoplegia, Blindness, and Deafness: Case Report.\",\"authors\":\"Amitouj S Sidhu, Charles E L Walker, Thomas D Riisfeldt, Peter J Tweedie, Natasha Gerbis, Emily J Sutherland, Neil G Simon, Lucy K Somerville, Ross Bradbury, Raymond Cook, Jonathon Parkinson, Robert Goetti, Ian C Francis\",\"doi\":\"10.1159/000538821\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Streptococcal meningoencephalitis (SME) is a rare, and frequently lethal, acute infection, and inflammation of the central nervous system parenchyma, with associated meningeal involvement. 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引用次数: 0
摘要
导言:链球菌脑膜脑炎(SME)是一种罕见的、经常致命的急性感染,是中枢神经系统实质的炎症,伴有脑膜受累。尽管可以使用抗菌药和皮质类固醇治疗,但细菌性脑膜脑炎的发病率和死亡率通常都很高。虽然肺炎链球菌是公认的细菌性脑膜炎的致病菌,但直接扩展到中枢神经系统实质的情况却很少见:病例介绍:一名 49 岁的男性患者因突发剧烈头痛、发热、颈部僵硬和意识减退而就诊。该患者的 SME 表现为双侧瞳孔-第三神经节麻痹、壁眼双侧核间性眼肌麻痹(WEBINO)、双侧失明、双侧耳聋、右侧下运动神经元面瘫和四肢上运动神经元体征。最初,患者对大剂量静脉注射抗生素产生了部分反应,但随着皮质类固醇的静脉注射,患者的神经和神经眼科功能障碍得到了进一步的实质性缓解:本病例强调了多学科诊断和治疗干预对并发双侧瞳孔牵涉第三神经麻痹、WEBINO、双侧失明、双侧失聪、右侧下运动神经元面瘫和上运动神经元体征的SME病例的益处。这似乎是首例报告的 SME 合并这种罕见的神经眼科异常的病例。
Successful Management of Acute Streptococcal Meningoencephalitis Complicated by Bilateral Third-Nerve Palsies, Wall-Eyed Bilateral Internuclear Ophthalmoplegia, Blindness, and Deafness: Case Report.
Introduction: Streptococcal meningoencephalitis (SME) is a rare, and frequently lethal, acute infection, and inflammation of the central nervous system parenchyma, with associated meningeal involvement. Bacterial meningoencephalitis is generally associated with high rates of morbidity and mortality, despite available antimicrobial and corticosteroid treatments. While Streptococcus pneumoniae is well recognised to cause bacterial meningitis, direct extension into the central nervous system parenchyma is rare.
Case presentation: A previously well 49-year-old man presented with sudden onset severe headache, fevers, neck stiffness, and reduced consciousness. The manifestations of SME in this patient were bilateral pupil-involving third-nerve palsies, wall-eyed bilateral internuclear ophthalmoplegia (WEBINO), bilateral blindness, bilateral deafness, a right lower motor neuron facial palsy, and upper motor neuron signs in his limbs. Initially, a partial response to high dose intravenous antibiotics occurred, but with administration of intravenous corticosteroids, further substantial resolution of the patient's neurological and neuro-ophthalmological deficits occurred.
Conclusion: This case highlights the benefit of multidisciplinary diagnostic and therapeutic interventions in a case of SME complicated by bilateral pupil-involving third-nerve palsies, WEBINO, bilateral blindness, bilateral deafness, a right lower motor neuron facial palsy, and upper motor neuron signs. It appears to be the first reported case of SME with this rare collection of neuro-ophthalmological abnormalities.
期刊介绍:
This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of ophthalmology, including prevention, diagnosis, treatment, toxicities of therapy, supportive care, quality-of-life, and survivorship issues. The submission of negative results is strongly encouraged. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed. The intent of the journal is to provide clinicians and researchers with a tool to disseminate their personal experiences to a wider public as well as to review interesting cases encountered by colleagues all over the world. Universally used terms can be searched across the entire growing collection of case reports, further facilitating the retrieval of specific information. Following the open access principle, the entire contents can be retrieved at no charge, guaranteeing easy access to this valuable source of anecdotal information at all times.