keyword
https://read.qxmd.com/read/38646403/a-case-of-mri-negative-leptomeningeal-disease-from-non-small-cell-lung-cancer
#21
Andrew Kokavec, Joanna Laba
Leptomeningeal disease (LMD) is a rare complication of advanced non-small cell lung cancer (NSCLC), associated with a poor prognosis. We report the case of a 55-year-old man, who presented with a metastatic NSCLC with limited brain and abdominal metastases. He was treated with both chemoimmunotherapy and stereotactic radiotherapy (SRT) to the brain. Despite treatment, the patient experienced progressive neurological symptoms not in keeping with the extent of disease seen on imaging of the brain. Due to this incongruence between symptoms and radiologic findings, he underwent a lumbar puncture, which had positive cytology for LMD...
March 2024: Curēus
https://read.qxmd.com/read/38646354/posterior-reversible-encephalopathy-syndrome-presenting-as-delirium-with-psychosis-and-agitation-in-the-postpartum-period
#22
Talitha West, Jason Christopher, Stanislav Arkhipov, Daniel Erickson, Adriana Fitzsimmons
Posterior reversible encephalopathy syndrome (PRES), which was first described in 1996, is a neurologic condition characterized by a combination of clinical and neuroimaging findings. PRES may arise in the context of preeclampsia, eclampsia, renal failure, and sepsis, among other conditions. Neuropsychiatric symptoms of PRES include altered mental status, agitation, and in some cases psychosis. PRES occurring in the postpartum period is understudied, especially with regard to its psychiatric manifestations...
March 2024: Curēus
https://read.qxmd.com/read/38646306/restoring-functionality-a-case-report-on-physiotherapeutic-rehabilitation-for-l5-s1-anterolisthesis-management
#23
Mansee S Dangare, Nikita Gangwani, Priya Tikhile, Anushka P Bhagwat, Mitushi Deshmukh, Pratik Phansopkar
Anterolisthesis is a condition where a vertebra in the spine slips forward relative to the vertebra below it. Anterolisthesis is often described in terms of the direction of the slippage and the affected vertebrae, such as L5-S1 anterolisthesis, which indicates the slippage occurring between the fifth lumbar vertebra (L5) and the sacral bone (S1). Anterolisthesis can result from various factors, trauma, or congenital abnormalities. The symptoms associated with anterolisthesis can include lower back pain, stiffness, muscle tightness, and neurological symptoms if the slippage compresses nearby nerves...
March 2024: Curēus
https://read.qxmd.com/read/38646280/trivial-neck-bite-resulting-in-a-stroke-in-an-18-month-old-child-a-case-report
#24
Ruthwik Duvuru, Ahmad Alawadhi, Shivani Raju, Haitham ElBashir
Stroke is often viewed as a diagnosis found In the elderly with or without comorbidities, but it is vital to not rule it out in a pediatric patient presenting with signs and symptoms of stroke. Here, we present a case of an 18-month-old boy who arrived at the emergency department with left arm weakness and left-sided seizures a few minutes after a right-sided trivial neck bite that was initially overlooked by the parents until symptoms occurred. Urgent imaging further with a computed tomography scan of the brain revealed a hypodense lesion in the area covering the lateral part of the frontal lobe, insula, and parietal cortex of the right hemisphere...
March 2024: Curēus
https://read.qxmd.com/read/38646272/post-covid-19-neurological-sequelae-of-polyneuropathy-and-encephalitis-a-comprehensive-case-report
#25
Sebastian L Manuel, Jenna Sapone, Frank Lin, Mathai Chalunkal
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, commonly known as COVID-19, has been associated with various neurological complications. However, the mechanisms underlying these neurological manifestations remain incompletely understood. We present a case of a 63-year-old male who was admitted to the intensive care unit with severe COVID-19 pneumonia. Following recovery from respiratory symptoms, he was found to have weakness in the limbs. Months later, he also developed altered mental status, hallucinations, and behavioral changes...
March 2024: Curēus
https://read.qxmd.com/read/38646216/scrub-typhus-presenting-as-bilateral-sixth-nerve-palsy
#26
Sukriti Bhattacharjee, Bibhu Debbarma, Rajesh K Debbarma, Gourab Das
Scrub typhus, a tropical rickettsial infection, can have various neurological manifestations. Here, we present the case of an otherwise healthy 19-year-old female who presented to the emergency department with fever, headache, and diplopia. On examination, she was found to have bilateral sixth nerve palsy and bilateral papilledema. Initial unenhanced CT of the brain and CT venogram were unremarkable. The cerebrospinal fluid study was normal. Later, bloodwork revealed high titers of Orientia tsutsugamushi antibody...
March 2024: Curēus
https://read.qxmd.com/read/38645962/atypical-brain-mri-findings-in-a-patient-with-treatment-responsive-anti-iglon5-disease
#27
Moein Zandiehvakili, Cathy Kexin Cui, Bronte Jeffrey, Florence Ching-Fen Chang, Jonathan Emerson, Samuel Conyngham
Anti-IgLON5 disease is a rare autoimmune neurological condition which was relatively recently described in the literature. This syndrome encompasses a range of clinical manifestations with most cases showing unremarkable findings on brain magnetic resonance imaging (MRI). Here, we report a case of a 61-year-old female patient with unique brain MRI features that, to the best of our knowledge, has not been reported in the literature before. Following treatment including immunotherapy, the patient experienced significant improvement clinically accompanied by radiological improvement on the follow-up imaging...
July 2024: Radiology Case Reports
https://read.qxmd.com/read/38645955/malignant-transformation-of-vestibular-schwannoma-after-radiation-therapy
#28
Anastasia Drakos, Augusto Goncalves Filho, John Woulfe, Paulo Puac Polanco, Eduardo Portela de Oliveira
Stereotactic radiosurgery (SRS) is an effective treatment for vestibular schwannomas, offering high rates of tumor control and low neurological risks. Long-term complications of SRS are not fully understood, with several cases of malignant transformation reported in the literature. We report the case of a 50-year-old female with no prior history of neurofibromatosis who presented in 2013 with MRI evidence of a benign vestibular schwannoma. Despite treatment with CyberKnife SRS, she presented 6 years later with new onset neurologic symptoms...
July 2024: Radiology Case Reports
https://read.qxmd.com/read/38645946/double-whammy-delayed-cerebral-ischemia-of-a-19-year-old-secondary-to-sinogenic-complications-from-an-uncommon-bacterial-sinusitis-arcanobacterium-haemolyticum
#29
Soon Jie Chin, Damien Horton
Arcanobacterium haemolyticum , found as normal flora in healthy individuals, is an unusual culprit for pharyngitis and sinusitis in young adults, rarely leading to severe infections. Here, we present a singular case involving a 19-year-old immunocompetent male who experienced complications arising from A haemolyticum sinusitis, leading to orbital and intracranial sinogenic complications. The patient developed severe cerebral vasospasm with delayed cerebral ischemia, necessitating aggressive management encompassing daily catheter-directed intra-arterial infusions, surgical source control, and maximal medical therapy...
July 2024: Radiology Case Reports
https://read.qxmd.com/read/38645817/extracorporeal-shock-wave-lithotripsy-ureterolithotripsy-and-percutaneous-nephrolithotripsy-challenges-in-managing-spinal-cord-neuropathy-patients-lessons-learned-from-a-scoping-review
#30
REVIEW
Daniele Castellani, Carlo Brocca, Demetra Fuligni, Carlo Giulioni, Angelo Antezza, Angelo Cormio, Arianna Rubino, Lucia Pitoni, Virgilio De Stefano, Giulio Milanese, Luigi Cormio, Bhaskar Kumar Somani, Vineet Gauhar, Andrea Benedetto Galosi
INTRODUCTION: We aim to review the outcomes of shock wave lithotripsy (SWL), ureteroscopy, and percutaneous nephrolithotripsy (PCNL) for renal and ureteral stones in spinal cord neuropathy patients (SNP). MATERIAL AND METHODS: A literature search was performed on 8th March 2023 using PubMed, EMBASE, and Google Scholar with no date limit. Preclinical/animal studies, reviews, letters to the editor, case reports, and meeting abstracts were excluded. Only English papers were accepted...
2024: Central European Journal of Urology
https://read.qxmd.com/read/38645745/a-hidden-pathophysiology-of-endolymphatic-hydrops-case-report-of-a-patient-with-spontaneous-intracranial-hypotension-presenting-with-sudden-sensorineural-hearing-loss-with-vertigo
#31
JOURNAL ARTICLE
Jong Kwan Kim, Ho Yun Lee, Ha Youn Kim, Min Young Kwak
Spontaneous intracranial hypotension (SIH) is characterized by decreased cerebrospinal fluid (CSF) volume due to leakage through the dural membrane. We present the case of a patient with SIH manifested by fluctuating low-frequency hearing loss, tinnitus, and vertigo. In this patient, endolymphatic hydrops in the cochlea and saccule were visualized by means of a special sequence of inner ear magnetic resonance imaging scans, with a gadolinium-based contrast agent administered intravenously. Endolymphatic hydrops is a potential underlying pathophysiology of SIH-associated hearing impairment...
2024: Frontiers in Neurology
https://read.qxmd.com/read/38645602/plasma-cell-myeloma-in-a-9-year-old-male-case-report-and-literature-review
#32
Kato Ronald, Ambaru Jacinta, Ssebagala Umaru
KEY CLINICAL MESSAGE: Plasma cell myeloma is a rare entity in the pediatric population. The peak incidence is in the seventh decade, with less than 2% of cases occurring in patients under the age of 40. It is worth noting that any destructive bony lesion in a child should be investigated. ABSTRACT: Plasma cell myeloma (multiple myeloma) is the most common form of plasma cell neoplasm. It is a rare entity in young patients. The peak incidence is in the seventh decade, with less than 2% of cases occurring in patients under the age of 40...
April 2024: Clinical Case Reports
https://read.qxmd.com/read/38645407/fever-and-increased-gastrointestinal-uptake-on-positron-emission-tomography-after-anti-tumour-necrosis-factor-therapy-a-case-report-of-whipple-s-disease
#33
Arteen Arzivian, Brett Jones, Fredrick Joshua, Miriam Paul, Thomas Lynch, Martin Brown, Robin Gasiorowski
INTRODUCTION: Whipple's disease is a rare condition that can present with atypical and non-specific features requiring a high index of suspicion for diagnosis. CASE PRESENTATION: We present a case of a man in his 40s with peripheral arthritis and bilateral sacro-ileitis for 4-5 years that was treated with an anti-tumour necrosis factor therapy, which led to worsening of his symptoms, elevation of the inflammatory markers, and the development of fever, night sweats, anorexia, and a significant weight loss...
2024: Case Reports in Gastroenterology
https://read.qxmd.com/read/38644908/spinal-lymphangiomas-case-based-review-of-a-chameleonic-disease-entity
#34
REVIEW
François Yves Legninda Sop, Alberto Benato, Blaise Koumare Izoudine, Kifah Khouri, Anna Marangon, Flavia Fraschetti, Nicolas Lonjon, Stefano Ferraresi
PURPOSE: Lymphangiomas are benign hamartomas in the spectrum of lymphatic malformations, exhibiting multifaceted clinical features. Spinal involvement is exceedingly rare, with only 35 cases reported to date. Both due to their rarity and chameleonic radiologic features, spinal lymphangiomas (SLs) are usually misdiagnosed; postoperatively, surgeons are thus confronted with an unexpected histopathological diagnosis with sparse pertinent literature and no treatment guidelines available. METHODS: Here, we report the case of a 67-year-old female who underwent surgery for a T6-T7 epidural SL with transforaminal extension, manifesting with spastic paraparesis...
2024: Journal of Craniovertebral Junction and Spine
https://read.qxmd.com/read/38644331/ultra-high-field-7-tesla-magnetic-resonance-imaging-in-fragile-x-tremor-ataxia-syndrome-fxtas
#35
JOURNAL ARTICLE
Dhairya A Lakhani, Amit K Agarwal, Erik H Middlebrooks
Fragile X tremor/ataxia syndrome (FXTAS) is an adult-onset neurodegenerative disorder characterized by premutation expansion of fragile X mental retardation 1 (FMR1) gene. It is a common single-gene cause of tremor, ataxia, and cognitive decline in adults. FXTAS affects the central, peripheral and autonomic nervous systems, leading to a range of neurological symptoms from dementia to dysautonomia. A characteristic imaging feature of FXTAS is symmetric T2 hyperintensity in the deep white matter of the cerebellar hemispheres and middle cerebral peduncle...
April 21, 2024: Neuroradiology Journal
https://read.qxmd.com/read/38643683/chronic-idiopathic-urinary-retention-comorbidity-and-outcome-in-102-individuals
#36
JOURNAL ARTICLE
Fintan Milligan, Charlotte Whittingham, Voula Granitsitotis, Helen Simpson, Julie Woodfield, Alan Carson, Jon Stone, Ingrid Hoeritzauer
OBJECTIVES: Chronic Idiopathic urinary retention is poorly understood. One small study suggests higher than expected rates of functional neurological disorder and pain comorbidity which may have implications for understanding the disorder. We investigated the frequency of functional neurological disorder, chronic pain other medical and psychiatric comorbidity, triggers of urinary retention, results of urodynamic assessment, medication history, management, and outcome in patients with chronic idiopathic urinary retention...
April 6, 2024: Journal of Psychosomatic Research
https://read.qxmd.com/read/38643659/current-challenges-in-focal-epilepsy-treatment-an-italian-delphi-consensus
#37
JOURNAL ARTICLE
Giancarlo Di Gennaro, Simona Lattanzi, Oriano Mecarelli, Francesco Saverio Mennini, Federico Vigevano
BACKGROUND: Epilepsy, a globally prevalent neurological condition, presents distinct challenges in management, particularly for focal-onset types. This study aimed at addressing the current challenges and perspectives in focal epilepsy management, with focus on the Italian reality. METHODS: Using the Delphi methodology, this research collected and analyzed the level of consensus of a panel of Italian epilepsy experts on key aspects of focal epilepsy care. Areas of focus included patient flow, treatment pathways, controlled versus uncontrolled epilepsy, follow-up protocols, and the relevance of patient-reported outcomes (PROs)...
April 20, 2024: Epilepsy & Behavior: E&B
https://read.qxmd.com/read/38643655/sequential-treatment-of-concomitant-odontoid-fracture-and-lower-cervical-fracture-dislocation-a-case-report
#38
Yuanchen Zhu, Jin Qian, Hanfeng Hu, Feng Zhou, Huilin Yang, Jinhui Shi
INTRODUCTION AND IMPORTANCE: To report the sequential treatment of a Type II odontoid fracture combined with a severe lower cervical (C6-7) fracture-dislocation featuring bilateral facet joint interlocking. CASE PRESENTATION: A 58-year-old male who had suffered an injury in a car accident, He presented neck pain and extremity paralysis. His neurological function was classified as per the American Spinal Injury Association (ASIA) impairment scale as Grade A, indicating complete deficits below the C6 spinal cord level...
April 20, 2024: International Journal of Surgery Case Reports
https://read.qxmd.com/read/38643005/prehospital-identification-of-intracerebral-haemorrhage-a-scoping-review-of-early-clinical-features-and-portable-devices
#39
REVIEW
Mohammed Almubayyidh, Ibrahim Alghamdi, Adrian Robert Parry-Jones, David Jenkins
INTRODUCTION: Prehospital identification of intracerebral haemorrhage (ICH) in suspected stroke cases may enable the initiation of appropriate treatments and facilitate better-informed transport decisions. This scoping review aims to examine the literature to identify early clinical features and portable devices for the detection of ICH in the prehospital setting. METHODS: Three databases were searched via Ovid (MEDLINE, EMBASE and CENTRAL) from inception to August 2022 using prespecified search strategies...
April 19, 2024: BMJ Open
https://read.qxmd.com/read/38642630/hook-effect-in-maglumi-immunoassay-for-serum-anti-gad-antibodies-in-neurological-disorders-when-wrong-matrix-is-the-right-choice
#40
G Musso, M Zoccarato, N Gallo, M Plebani, D Basso
Antibodies against glutamic acid decarboxylase (anti-GAD) are a valuable diagnostic tool to detect severe autoimmune conditions as type 1 diabetes mellitus (T1DM) and anti-GAD related neurological disorders, having the latter more often anti-GAD concentrations in serum multiple times higher than in the former. Automated immunoassays, either with ELISA or chemiluminescent technology, are validated for diagnostic use in serum with analytical ranges suitable for T1DM diagnosis. In a patient presenting with a suspected autoimmune ataxia, anti-GAD testing on an automated chemiluminescent immunoassay (CLIA) resulted in slightly abnormal concentrations in serum (39...
April 18, 2024: Clinica Chimica Acta; International Journal of Clinical Chemistry
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