Neurohospitalist最新文献

筛选
英文 中文
Focal Status Epilepticus and Extreme Delta Brush Associated With Thrombotic Thrombocytopenic Purpura. 与血栓性血小板减少性紫癜相关的局灶性癫痫状态和极度德尔塔刷状反应
IF 1
Neurohospitalist Pub Date : 2024-07-01 Epub Date: 2024-04-01 DOI: 10.1177/19418744241245454
Lauren E Yap, Huanwen Chen, Sarah Ganji, Samuel E Calabria, Edwin J Serrano, Andrew B Stemer, Francis G Tirol, Noushin Jazebi
{"title":"Focal Status Epilepticus and Extreme Delta Brush Associated With Thrombotic Thrombocytopenic Purpura.","authors":"Lauren E Yap, Huanwen Chen, Sarah Ganji, Samuel E Calabria, Edwin J Serrano, Andrew B Stemer, Francis G Tirol, Noushin Jazebi","doi":"10.1177/19418744241245454","DOIUrl":"10.1177/19418744241245454","url":null,"abstract":"<p><p>Acute focal neurological deficits demand immediate evaluation. In this report, we present the case of a woman 20-some years of age with a history of hemolytic anemia and thrombocytopenia who presented with altered mental status and focal neurological deficits including aphasia, acute left gaze preference, right homonymous hemianopsia, right lower facial weakness, and right arm and leg weakness. Extensive neurological and hematological workup revealed that the patient suffered from focal status epilepticus associated with an extreme delta brush patten on electroencephalogram, likely secondary to thrombotic thrombocytopenic purpura. This case underscores the connection between hematological disorders and the neurological axis, emphasizing the critical role of integrating the neurological examination and neuroimaging findings to formulate an effective management plan.</p>","PeriodicalId":46355,"journal":{"name":"Neurohospitalist","volume":"14 3","pages":"356-360"},"PeriodicalIF":1.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11181973/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141421373","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Anti-LGI-1 Limbic Encephalitis and Autoimmune Epilepsy Following a Third Dose of COVID-19 Vaccination: A Case Report. 接种第三剂 COVID-19 疫苗后出现抗 LGI-1 边缘脑炎和自身免疫性癫痫:病例报告。
IF 1
Neurohospitalist Pub Date : 2024-07-01 Epub Date: 2024-02-20 DOI: 10.1177/19418744241234100
Gerry Mullan, Michael Kinney
{"title":"Anti-LGI-1 Limbic Encephalitis and Autoimmune Epilepsy Following a Third Dose of COVID-19 Vaccination: A Case Report.","authors":"Gerry Mullan, Michael Kinney","doi":"10.1177/19418744241234100","DOIUrl":"10.1177/19418744241234100","url":null,"abstract":"<p><p>Anti-leucine rich glioma inactivated 1 (LGI-1) autoimmune encephalitis (AE) typically presents with cognitive impairment, faciobrachial dystonic seizures (FBDS) and hyponatraemia. Reports are growing of neurological complications following coronavirus disease 2019 (COVID-19) vaccination. Here we describe a 50 year old man who developed anti-LGI-1 limbic encephalitis and autoimmune epilepsy 4 days following a dose of the mRNA Pfizer COVID-19 vaccine (of note, his first two vaccinations were viral vector ChAdOX1-S). He presented with focal aware seizures characterised by short-lived episodes of confusion, emotional distress and déjà vu associated with palpitations. He also reported subacute progressive amnesia. He responded well to high-dose steroid and subsequent immunoglobulin therapy. To our knowledge, this is the first reported case of anti-LGI-1 AE following a mixed COVID-19 vaccination regimen. We aim to complement the early literature on this post-COVID-19 vaccination phenomenon.</p>","PeriodicalId":46355,"journal":{"name":"Neurohospitalist","volume":"14 3","pages":"332-335"},"PeriodicalIF":1.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11181977/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141421358","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical Reasoning: A 38-Year-Old Woman Presenting With Acute Hyperkinetic Movements of Her Right Arm. 临床推理:一名 38 岁女性出现急性右臂过度运动。
IF 1
Neurohospitalist Pub Date : 2024-07-01 Epub Date: 2024-03-18 DOI: 10.1177/19418744241240524
Dylan Ryan, Tasnim Mushannen, Scott Le
{"title":"Clinical Reasoning: A 38-Year-Old Woman Presenting With Acute Hyperkinetic Movements of Her Right Arm.","authors":"Dylan Ryan, Tasnim Mushannen, Scott Le","doi":"10.1177/19418744241240524","DOIUrl":"10.1177/19418744241240524","url":null,"abstract":"<p><p>We present a case report of a 38-year-old woman who presented to the hospital with acute onset high amplitude, non-rhythmic, hyperkinetic movements of the right upper extremity, abnormal sensation of the right upper extremity from the elbow to the hand, and the inability to recognize her hand without visual input. This case discusses the differential diagnoses of acute hyperkinetic movement disorders and concurrent alien-limb in a patient presenting within the time window for vascular intervention. Readers are led through the reasoning behind acute interventional decision-making in a patient with a rare presentation. Workup reveals the eventual diagnosis.</p>","PeriodicalId":46355,"journal":{"name":"Neurohospitalist","volume":"14 3","pages":"308-311"},"PeriodicalIF":1.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11181980/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141421371","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Super Refractory Status Epilepticus Improved After Emergency Use of Ganaxolone: Case Report. 紧急使用甘珀酸后,超级难治性癫痫状态得到改善:病例报告。
IF 1
Neurohospitalist Pub Date : 2024-07-01 Epub Date: 2024-02-20 DOI: 10.1177/19418744241232181
Jody Manners, Emily Jusuf, Gunjan Y Parikh, Maciej Gasior, Henrikas Vaitkevicius, Nicholas A Morris
{"title":"Super Refractory Status Epilepticus Improved After Emergency Use of Ganaxolone: Case Report.","authors":"Jody Manners, Emily Jusuf, Gunjan Y Parikh, Maciej Gasior, Henrikas Vaitkevicius, Nicholas A Morris","doi":"10.1177/19418744241232181","DOIUrl":"10.1177/19418744241232181","url":null,"abstract":"<p><p>We present a case of a 34-year-old man with epilepsy who developed super refractory status epilepticus in the setting of COVID-19 pneumonia in whom aggressive therapy with multiple parenteral, enteral, and non-pharmacologic interventions were utilized without lasting improvement in clinical examination or electroencephalogram (EEG). The patient presented with multiple recurrences of electrographic status epilepticus throughout a prolonged hospital stay. Emergency use authorization was obtained for intravenous ganaxolone, a neuroactive steroid that is a potent modulator of both synaptic and extrasynaptic GABA<sub>A</sub> receptors. Following administration of intravenous ganaxolone according to a novel dosing paradigm, the patient showed sustained clinical and electrographic improvement.</p>","PeriodicalId":46355,"journal":{"name":"Neurohospitalist","volume":"14 3","pages":"327-331"},"PeriodicalIF":1.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11181981/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141421375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Short Report: Clinical Features and Epilepsy Monitoring in an Adult With 22q11.2 Deletion Syndrome. 简短报告:一名 22q11.2 缺失综合征成人的临床特征和癫痫监测。
IF 1
Neurohospitalist Pub Date : 2024-07-01 Epub Date: 2024-01-17 DOI: 10.1177/19418744241228618
Mike W Zhang, Stephanie T Bustros, Tyler E Gaston, Maria Descartes, Shruti P Agnihotri
{"title":"Short Report: Clinical Features and Epilepsy Monitoring in an Adult With 22q11.2 Deletion Syndrome.","authors":"Mike W Zhang, Stephanie T Bustros, Tyler E Gaston, Maria Descartes, Shruti P Agnihotri","doi":"10.1177/19418744241228618","DOIUrl":"10.1177/19418744241228618","url":null,"abstract":"<p><strong>Background: </strong>22q11.2 microdeletion is the most common microdeletion syndrome in humans with a prevalence of 13 per 100 000 live births, and it is a multisystem condition with variable phenotypic presentations.</p><p><strong>Methods: </strong>We present a case of an adult patient with Dandy-Walker syndrome who presented to our epilepsy clinic with 2 years of new-onset seizures and cognitive decline and 1 year of psychotic symptoms.</p><p><strong>Results: </strong>Patient had a non-revealing autoimmune and malignancy work-up. Continuous scalp vEEG study showed bursts of 1-2 Hz generalized fronto-centrally predominant spike or polyspike and slow wave discharges. Several myoclonic jerks were time-locked with the generalized discharges indicative of cortical myoclonus. MRI brain revealed periventricular nodular heterotopia in addition to findings suggestive of Dandy-Walker syndrome. Array-based comparative genomic hybridization demonstrated a 22q11.2 microdeletion seen in 22q11.2 deletion syndrome.</p><p><strong>Conclusion: </strong>Our case illustrates the challenges of diagnosing genetic disorders in adults especially when the initial diagnosis is dependent on a number of factors, including the patient's age, the severity of the phenotypic features, and the awareness of the physician.</p>","PeriodicalId":46355,"journal":{"name":"Neurohospitalist","volume":"14 3","pages":"273-277"},"PeriodicalIF":1.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11181976/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141421374","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Trismus as the Initial Presentation of Anti-Hu Paraneoplastic Neurological Syndrome. 作为抗胡副肿瘤性神经综合征最初表现的 "三体症"。
IF 1
Neurohospitalist Pub Date : 2024-07-01 Epub Date: 2024-03-04 DOI: 10.1177/19418744241237593
Witoon Mitarnun, Metha Apiwattanakul, Narin Chindavech, Benyapha Sombat, Suttanon Jantapatsakun, Pheeracha Sornnuwat
{"title":"Trismus as the Initial Presentation of Anti-Hu Paraneoplastic Neurological Syndrome.","authors":"Witoon Mitarnun, Metha Apiwattanakul, Narin Chindavech, Benyapha Sombat, Suttanon Jantapatsakun, Pheeracha Sornnuwat","doi":"10.1177/19418744241237593","DOIUrl":"10.1177/19418744241237593","url":null,"abstract":"<p><p>A 73-year-old man presented with subacute trismus and pancerebellar dysfunction. Brain imaging and routine blood test results were unremarkable. Chest computed tomography revealed an indistinctly enhancing 4.7 × 2.5 × 1.8-cm<sup>3</sup> pulmonary mass in the right upper lung, with enlarged right paratracheal and hilar lymph nodes. Biopsy of the right supraclavicular lymph node confirmed metastatic carcinoma, with differential diagnoses of small cell carcinoma and poorly differentiated carcinoma, indicating lung cancer as the primary source. Paraneoplastic immunohistochemistry screening revealed anti-Hu antibodies in the serum at a titer of 1:7680 (normal range <1:240) and in the cerebrospinal fluid (CSF) at a titer of 1:256 (normal range <1:2). The line blot method yielded positive results for anti-Zic4 antibodies in serum, with a titer of >1:10 (normal range <1:10), whereas CSF anti-Zic4 was negative (normal range <1:2). The patient developed non-responsive hospital-acquired pneumonia and respiratory failure, and discharged himself against medical advice. This rare case indicates that trismus can be an initial manifestation of anti-Hu paraneoplastic neurological syndrome, and emphasizes the importance of clinical awareness.</p>","PeriodicalId":46355,"journal":{"name":"Neurohospitalist","volume":"14 3","pages":"336-338"},"PeriodicalIF":1.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11181965/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141421376","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Elsberg Syndrome With Albuminocytologic Dissociation - A Guillain-Barré Syndrome Mimic or Guillain-Barré Syndrome Variant? 伴有白蛋白细胞学分离的埃尔斯伯格综合征--吉兰-巴雷综合征的拟态还是吉兰-巴雷综合征的变异?
IF 1
Neurohospitalist Pub Date : 2024-07-01 Epub Date: 2024-02-20 DOI: 10.1177/19418744241233621
Joseph M Ferrara, Courtney Litchmore, Smit Shah, Jeffery Myers, Khalil Ali
{"title":"Elsberg Syndrome With Albuminocytologic Dissociation - A Guillain-Barré Syndrome Mimic or Guillain-Barré Syndrome Variant?","authors":"Joseph M Ferrara, Courtney Litchmore, Smit Shah, Jeffery Myers, Khalil Ali","doi":"10.1177/19418744241233621","DOIUrl":"10.1177/19418744241233621","url":null,"abstract":"<p><strong>Introduction: </strong>Elsberg Syndrome is a presumed infectious lumbosacral radiculitis, with or without accompanying lumbar myelitis, that is often attributed to herpes simplex virus type 2 (HSV-2).</p><p><strong>Case: </strong>A 58-year-old man presented with lower extremity anesthesia, ataxic gait, radiological evidence of radiculitis, and CSF albuminocytologic dissociation. Polymerase chain reaction testing of CSF confirmed HSV-2 infection.</p><p><strong>Conclusion: </strong>A variety of presentations are reported within the scope of Elsberg Syndrome, potentially with distinct disease mechanisms. Delayed onset of neurological symptoms after resolution of rash and absence of pleocytosis raises the possibility that some patients meeting criteria for Elsberg Syndrome have a post-infectious immune-mediated neuropathy. We advise a lower threshold for PCR testing of herpes viruses in patients with acute neuropathy and albuminocytologic dissociation, particularly in cases with early sacral involvement.</p>","PeriodicalId":46355,"journal":{"name":"Neurohospitalist","volume":"14 3","pages":"322-326"},"PeriodicalIF":1.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11181979/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141421372","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Neuromyelitis Optica Spectrum Disorder Resembling Wernicke's Encephalopathy: A Case Report and Review of the Literature. 类似韦尼克脑病的神经脊髓炎谱系障碍:病例报告与文献综述。
IF 1
Neurohospitalist Pub Date : 2024-04-01 Epub Date: 2024-01-16 DOI: 10.1177/19418744241228004
Sloan Lynch, Nil Saez Calveras, Anik Amin
{"title":"Neuromyelitis Optica Spectrum Disorder Resembling Wernicke's Encephalopathy: A Case Report and Review of the Literature.","authors":"Sloan Lynch, Nil Saez Calveras, Anik Amin","doi":"10.1177/19418744241228004","DOIUrl":"https://doi.org/10.1177/19418744241228004","url":null,"abstract":"<p><p>We describe a case of Neuromyelitis Optica Spectrum Disorder (NMOSD) mimicking Wernicke's Encephalopathy (WE) to highlight an atypical presentation of NMOSD. A 39-year-old female presented with subacute encephalopathy and progressive ophthalmoplegia. Her MRI revealed T2 hyperintensities involving the mammillary bodies, periaqueductal grey matter, medial thalami, third ventricle, and area postrema. Whole blood thiamine levels were elevated and she did not improve with IV thiamine. CSF was notable for lymphocytic pleocytosis and elevated protein. She tested positive for serum Aquaporin-4 (AQP4) antibody. Subsequent imaging revealed multilevel lesions in the cervical and thoracic spinal cord. Her CSF GFAP antibody also came back positive. She steadily and significantly improved after high-dose IV steroids and plasmapheresis. She later started on chronic rituximab therapy. This represents a unique case of NMOSD presenting with the classical clinical and imaging features of WE, as opposed to the typical presenting symptoms of NMOSD. As such, demyelinating disorders should be considered when there is concern for diencephalic and midline pathologies, particularly without classic WE risk factors. Conversely, clinicians should be aware of secondary nutritional complications arising from severe area postrema syndrome.</p>","PeriodicalId":46355,"journal":{"name":"Neurohospitalist","volume":"14 2","pages":"213-217"},"PeriodicalIF":1.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11040630/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140856233","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact of the COVID-19 Pandemic on Inpatient Utilization for Acute Neurologic Disease. 新冠肺炎疫情对急性神经系统疾病住院患者利用的影响
IF 0.9
Neurohospitalist Pub Date : 2024-01-01 Epub Date: 2023-08-17 DOI: 10.1177/19418744231196984
Alexander Yoo, Elan L Guterman, David Y Hwang, Robert G Holloway, Benjamin P George
{"title":"Impact of the COVID-19 Pandemic on Inpatient Utilization for Acute Neurologic Disease.","authors":"Alexander Yoo, Elan L Guterman, David Y Hwang, Robert G Holloway, Benjamin P George","doi":"10.1177/19418744231196984","DOIUrl":"10.1177/19418744231196984","url":null,"abstract":"<p><p><b>Background and Objective:</b> The initial months of the Corona Virus 2019 (COVID-19) pandemic resulted in decreased hospitalizations. We aimed to describe differences in hospitalizations and related procedures across neurologic disease. <b>Methods:</b> In our retrospective observational study using the California State Inpatient Database and state-wide population-level estimates, we calculated neurologic hospitalization rates for a control period from January 2019 to February 2020 and a COVID-19 pandemic period from March to December 2020. We calculated incident rate ratios (IRR) for neurologic hospitalizations using negative binomial regression and compared relevant procedure rates over time. <b>Results:</b> Population-based neurologic hospitalization rates were 29.1 per 100,000 (95% CI 26.9-31.3) in April 2020 compared to 43.6 per 100,000 (95% CI 40.4-46.7) in January 2020. Overall, the pandemic period had 13% lower incidence of neurologic hospitalizations per month (IRR 0.87, 95% CI 0.86-0.89). The smallest decreases were in neurotrauma (IRR 0.92, 95% CI 0.89-0.95) and neuro-oncologic cases (IRR 0.93, 95% CI 0.87-0.99). Headache admissions experienced the greatest decline (IRR 0.62, 95% CI 0.58-0.66). For ischemic stroke, greater rates of endovascular thrombectomy (5.6% vs 5.0%; <i>P</i> < .001) were observed in the pandemic. Among all neurologic disease, greater rates of gastrostomy (4.0% vs 3.5%; <i>P</i> < .001), intubation/mechanical ventilation (14.3% vs 12.9%, <i>P</i> < .001), and tracheostomy (1.4 vs 1.2%; <i>P</i> < .001) were observed during the pandemic. <b>Conclusions:</b> During the first months of the COVID-19 pandemic there were fewer hospitalizations to varying degrees for all neurologic diagnoses. Rates of procedures indicating severe disease increased. Further study is needed to determine the impact on triage, patient outcomes, and cost consequences.</p>","PeriodicalId":46355,"journal":{"name":"Neurohospitalist","volume":"1 1","pages":"13-22"},"PeriodicalIF":0.9,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10790622/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41468783","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Neuromyelitis Optica Spectrum Disorder Management in the Setting of Chronic Hepatitis B and Latent Tuberculosis: A Case Report. 慢性乙型肝炎和潜伏性肺结核患者视神经脊髓炎谱系障碍的治疗:一例报告。
IF 0.9
Neurohospitalist Pub Date : 2023-10-01 Epub Date: 2023-05-04 DOI: 10.1177/19418744231171464
Dylan Sadowsky, Kevin Delijani, William Davis, Amy Safadi, Petra Brayo, Benjamin Osborne
{"title":"Neuromyelitis Optica Spectrum Disorder Management in the Setting of Chronic Hepatitis B and Latent Tuberculosis: A Case Report.","authors":"Dylan Sadowsky, Kevin Delijani, William Davis, Amy Safadi, Petra Brayo, Benjamin Osborne","doi":"10.1177/19418744231171464","DOIUrl":"10.1177/19418744231171464","url":null,"abstract":"<p><p>Neuromyelitis Optica Spectrum Disorder (NMOSD) is an inflammatory autoimmune disorder of the central nervous system, with optic neuritis and transverse myelitis as its most common presentations. Although immunomodulatory treatment options for NMOSD have expanded, preventing reactivation of latent infections in patients can be both a therapeutic challenge and a special consideration for the neurohospitalist in an inpatient setting. We present a challenging case of a NMOSD patient who presented to the emergency department with worsening weakness and numbness in the setting of an NMOSD pseudo-relapse, later found to have untreated latent tuberculosis (TB) and chronic hepatitis B (HBV). She was briefly treated with high-dose IV methylprednisolone, which was stopped after her symptoms and imaging became more consistent with a pseudo-relapse. After confirmation that neither HBV nor TB had reactivated, the patient was discharged on isoniazid and entecavir. A month later, the patient's symptoms were stable, and she was started on inebilizumab for relapse prevention of NMOSD. This case report is the first to highlight the therapeutic complexities of managing NMOSD that requires immunosuppression in the setting of preventing reactivation of both TB and HBV.</p>","PeriodicalId":46355,"journal":{"name":"Neurohospitalist","volume":"13 4","pages":"361-363"},"PeriodicalIF":0.9,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494824/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10239186","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信