keyword
https://read.qxmd.com/read/38434459/ramsay-hunt-syndrome-associated-with-varicella-zoster-virus-encephalitis-in-a-child
#21
Eman Y Ahmed, Hatem Al Rawahi, Fatema Al Amrani, Laila Al Masaoudi, Laila Al Yazidi
Ramsay Hunt syndrome (RHS) is a triad of peri-auricular pain, ipsilateral facial nerve palsy and vesicular rash around the ear pinna. It is caused by reactivation of varicella-zoster virus (VZV) that lies dormant in the geniculate ganglia. It can be complicated by VZV encephalitis rarely. We report the case of an 8-year-old previously healthy boy who presented to a tertiary care hospital in Muscat, Oman in 2021 with fever, progressive left ear pain, vesicular rash around his ear pinna and left-sided facial nerve palsy...
February 2024: Sultan Qaboos University Medical Journal
https://read.qxmd.com/read/38420103/viral-myositis-secondary-to-influenza-a-in-a-preschool-child-in-saudi-arabia-a-case-report
#22
Rawia F Albar, Rahaf A Hubayni, Raghad A Aldahhas, Elaf I Khshwry
Infective myositis is a rare complication of viral infection, occurring most commonly in children. Here, we present the first case report in Saudi Arabia that describes a four-year-old healthy female who presented to the emergency department with a history of fever associated with coryzal symptoms for four days and a one-day history of bilateral lower limb pain and an inability to walk without assistance. Lower limb pain was not associated with joint pain, swelling, or skin rashes. The respiratory virus panel was positive for influenza A, and she was found to have increased levels of creatine kinase (CK)...
January 2024: Curēus
https://read.qxmd.com/read/38401556/paediatric-maternal-and-congenital-mpox-a-systematic-review-and-meta-analysis
#23
JOURNAL ARTICLE
Nuria Sanchez Clemente, Charlotte Coles, Enny S Paixao, Elizabeth B Brickley, Elizabeth Whittaker, Tobias Alfven, Stephen Rulisa, Nelson Agudelo Higuita, Paul Torpiano, Priyesh Agravat, Emma V Thorley, Simon B Drysdale, Kirsty Le Doare, Jean-Jacques Muyembe Tamfum
BACKGROUND: Although mpox has been detected in paediatric populations in central and west Africa for decades, evidence synthesis on paediatric, maternal, and congenital mpox, and the use of vaccines and therapeutics in these groups, is lacking. A systematic review is therefore indicated to set the research agenda. METHODS: We conducted a systematic review and meta-analysis, searching articles in Embase, Global Health, MEDLINE, CINAHL, Web of Science, Scopus, SciELO, and WHO databases from inception to April 17, 2023...
February 21, 2024: Lancet Global Health
https://read.qxmd.com/read/38384617/plasma-exchange-in-pediatric-neurology-patients-a-single-center-experience
#24
JOURNAL ARTICLE
Maram A Aljezani, Faris Althubaiti, Latifah Alhamed, Abdulrahman Alharthi, Abdulaziz Alamoodi, Yousof Bakheet, Maha Badawi, Salwa Hindawi
BACKGROUND: Therapeutic plasma exchange (TPE) is a procedure involving the filtration of a patient's plasma to eliminate pathogenic components or address deficiencies. This technique finds varied indications in the pediatric age group, particularly in neuroinflammatory diseases. OBJECTIVES: The objective of this study is to delve into our local experience with TPE, focusing on indications, outcomes, and complications among children with neurological diseases at King Abdulaziz University Hospital (KAUH) in Jeddah, Saudi Arabia...
January 2024: Curēus
https://read.qxmd.com/read/38370132/drug-reaction-with-eosinophilia-and-systemic-symptoms-dress-syndrome-secondary-to-antimicrobial-therapy-in-pediatric-bone-and-joint-infections
#25
JOURNAL ARTICLE
Sema Yildirim Arslan, Zumrut Sahbudak Bal, Gizem Guner Ozenen, Nimet Melis Bilen, Gulhadiye Avcu, Ece Erci, Zafer Kurugol, Huseyin Gunay, İpek Tamsel, Ferda Ozkinay
BACKGROUND: Bone and joint infections are common in children, particularly those under 10 years of age. While antimicrobial therapy can often successfully treat these infections, surgical drainage may also be necessary. It is important to note that prolonged courses of treatment have been associated with adverse events and drug reactions. Among these, drug reactions with eosinophilia and systemic symptoms (DRESS) syndrome is particularly severe and potentially life-threatening. We aimed to evaluate the cases of DRESS syndrome that develop during the treatment of bone and joint infections...
February 2024: World Allergy Organization Journal
https://read.qxmd.com/read/38367318/clinical-observation-and-analysis-of-rash-caused-by-lacosamide-in-children-with-epilepsy
#26
JOURNAL ARTICLE
Yingying Guo, Yu Liu, Dan Li, Xueying Wang, Shaoping Huang, Lin Yang
PURPOSE: To draw clinical attention to rashes caused by lacosamide. METHODS: This retrospective analysis included patients admitted to the Department of Pediatrics, Second Affiliated Hospital of Xi'an Jiaotong University between January 2021 and September 2023. We focused on patients who developed rashes after lacosamide treatment and analyzed all patients who exhibited rashes after lacosamide treatment to analyze the risk factors. RESULTS: In total, 190 patients received lacosamide, of whom four developed allergies (2...
February 13, 2024: Seizure: the Journal of the British Epilepsy Association
https://read.qxmd.com/read/38355290/scoring-systems-for-prediction-of-malaria-and-dengue-fever-in-non-endemic-areas-among-travellers-arriving-from-tropical-and-subtropical-areas
#27
JOURNAL ARTICLE
Donya Satarvandi, Suzanne Desirée van der Werff, Pontus Nauclér, Helena Hildenwall, Klara Sondén
BACKGROUND: Fever is a common symptom among travellers returning from tropical/subtropical areas to Europe, and promptly distinguishing severe illnesses from self-limiting febrile syndromes is important but can be challenging due to non-specific clinical presentation. METHODS: A cross-sectional study enrolled adults and children who sought care during 2015-2020 at Karolinska University Hospital, Stockholm, Sweden with fever within 2 months after returning from travel to a tropical/subtropical area...
March 21, 2024: Emergency Medicine Journal: EMJ
https://read.qxmd.com/read/38322079/recurrent-hand-foot-and-mouth-disease-in-a-saudi-girl
#28
Lamia Alakrash, Maee Barakeh, Wasan I AlQahtani, Renad K AlKanaan
Hand, foot, and mouth disease (HFMD) is a viral illness that predominantly affects infants and children, causing blisters and sores on the hands, feet, and mouth. Recurrence is rare, but a case in a six-year-old girl in Saudi Arabia was reported. A six-year-old girl presented with a rash on her palms and soles, which was preceded by a mild sore throat and low-grade fever. She had been in contact with her two-year-old sister, who had similar symptoms but a different rash pattern.  During clinical examination, multiple erythematous deep-seated vesicles and papules were noted on the patient's palms and soles, with no involvement of mucous membranes or nails...
January 2024: Curēus
https://read.qxmd.com/read/38287358/kawasaki-disease-in-neonates-a-case-report-and-literature-review
#29
REVIEW
Mingjun Shen, Die Liu, Fang Ye, Jing Zhang, Jun Wang
BACKGROUND: Kawasaki disease (KD) is an acute systemic vasculitis of unknown etiology that affects infants and young children but is extremely rare in neonates, especially afebrile KD. We present a case of KD without fever in a neonate and review the literature on KD in neonates. CASE PRESENTATION: A newborn female was hospitalized because her peripheral blood leukocytes increased for half a day. The admission diagnosis was considered neonatal sepsis and bacterial meningitis...
January 29, 2024: Pediatric Rheumatology Online Journal
https://read.qxmd.com/read/38263944/-a-case-report-of-monkeypox-disease-in-an-adolescent
#30
JOURNAL ARTICLE
Leyla Beşel, Önder Kılıçaslan, Çiğdem Kırmacı, Didem Kızmaz İsançlı, Irmak Emre, Adem Karbuz
Monkeypox virus (MPXV) infection is a zoonotic disease characterized by smallpox-like rashes. It is endemic in Central and West Africa. The World Health Organization (WHO) declared the disease as an epidemic due to a significant increase in the number of reported cases, starting from Europe and spreading to other regions, particularly in certain areas, in May 2022. On July 23, 2022, it was recognized as a public health problem of international importance. Our country has also been affected by this epidemic, and the official number of reported cases is twelve...
January 2024: Mikrobiyoloji Bülteni
https://read.qxmd.com/read/38243323/establishment-and-analysis-of-a-novel-diagnostic-model-for-systemic-juvenile-idiopathic-arthritis-based-on-machine-learning
#31
JOURNAL ARTICLE
Pan Ding, Yi Du, Xinyue Jiang, Huajian Chen, Li Huang
BACKGROUND: Systemic juvenile idiopathic arthritis (SJIA) is a form of childhood arthritis with clinical features such as fever, lymphadenopathy, arthritis, rash, and serositis. It seriously affects the growth and development of children and has a high rate of disability and mortality. SJIA may result from genetic, infectious, or autoimmune factors since the precise source of the disease is unknown. Our study aims to develop a genetic-based diagnostic model to explore the identification of SJIA at the genetic level...
January 19, 2024: Pediatric Rheumatology Online Journal
https://read.qxmd.com/read/38214543/pediatric-drug-reaction-with-eosinophilia-and-systemic-symptoms-a-12-year-retrospective-study-in-a-tertiary-center
#32
JOURNAL ARTICLE
Susheera Chatproedprai, Nisha Tiasiri, Karaked Chantawarangkul, Siriwan Wananukul
Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a rare and severe adverse drug reaction involving multiple organs. Data on DRESS syndrome among children are currently limited. The purpose of this study was to determine the clinical features, causative drugs, systemic organ involvement, laboratory findings, disease severity score, and treatment outcomes in pediatric DRESS patients. The medical records of all pediatric DRESS patients, based on the RegiSCAR diagnostic criteria and admitted to King Chulalongkorn Memorial Hospital, Bangkok, Thailand from January 2010 to December 2021, were reviewed...
January 12, 2024: Journal of Dermatology
https://read.qxmd.com/read/38187006/clinical-and-molecular-characterization-of-children-and-adults-with-respiratory-bocavirus-infection-in-mexico-a-cross-sectional-nested-study-within-the-ili002-prospective-observational-study
#33
JOURNAL ARTICLE
Ana Estela Gamiño-Arroyo, José Arellano-Galindo, Paola Del Carmen Guerra-de-Blas, Ana M Ortega-Villa, Allyson Mateja, Beatriz Llamosas-Gallardo, Ana A Ortíz-Hernández, Rafael Valdéz-Vázquez, Alejandra Ramírez-Venegas, Arturo Galindo-Fraga, Ma Lourdes Guerrero, Pilar Ramos-Cervantes, Luis Mendoza-Garcés, Mónica González-Matus, Carmen Marroquín-Rojas, Juan Xicohtencatl-Cortes, Sara A Ochoa, Ariadna Cruz-Córdova, John H Powers, Guillermo Miguel Ruiz-Palacios, John Beigel, Sarbelio Moreno-Espinosa
BACKGROUND: Human Bocaviruses (HBoV) can cause acute respiratory tract infections. High coinfection rates cloud its pathogenicity. This study sought to describe the clinical features of HBoV1 disease in children and adults with Influenza-like illness (ILI), exploring associations between viral load, clinical features, and seasonality. METHODS: Patients who tested positive for HBoV1 by polymerase chain reaction, enrolled from April 2010 to March 2014 in the ILI002 prospective observational cohort study were included in this cross-sectional nested study...
January 2024: Lancet Reg Health Am
https://read.qxmd.com/read/38186808/six-month-outcome-of-multisystem-inflammatory-syndrome-with-persistent-neutropenia-in-neonate-a-case-report-and-review-of-literature
#34
Sandeep D Jhajra, Sanjay K Tanti, Chhavi Sauparna, Sarita Kumari, Md W Uddin, Kumar Diwakar
Multisystem inflammatory syndrome in Children (MIS-C) is a postinfectious immune mediated complications seen in children and develop after 4-6 weeks of severe acute respiratory syndrome coronavirus -2 (SARS-CoV-2) infection, however, it is rare in neonates. The index case was admitted at day 19 of life with complaints of fever, loose stools and rash. Baby was discharged after 1 weeks with diagnosis of Multisystem inflammatory syndrome with persistent neutropenia. We follow up the case at 6 weeks, 12 weeks and 6 months of life...
November 2023: Journal of Family Medicine and Primary Care
https://read.qxmd.com/read/38183017/tocilizumab-for-treating-mevalonate-kinase-deficiency-and-tnf-receptor-associated-periodic-syndrome-a-case-series-and-literature-review
#35
REVIEW
Yandie Li, Meiping Lu
BACKGROUND: Mevalonate kinase deficiency (MKD) and TNF receptor-associated periodic syndrome (TRAPS) are categorized as systemic autoinflammatory diseases (SAIDs), which are rare diseases characterized by early onset, severe conditions, and challenging diagnosis and treatment. Although different SAIDs have varying standard treatments, some SAIDs are poorly controlled after routine treatment, seriously affecting the growth and development of children and their quality of life. This study aims to provide more treatment strategies for SAIDs...
January 5, 2024: Pediatric Rheumatology Online Journal
https://read.qxmd.com/read/38161959/a-challenging-diagnosis-of-kawasaki-disease-shock-syndrome-complicated-by-bilateral-pleural-effusion-a-case-report-and-literature-review
#36
Linah Saleh Abbas Alghamdi, Ali Yahya B Alzahrani, Fahad A Alghamdi, Saleh J ALghamdi
Kawasaki disease (KD) is an acute illness primarily affecting children under the age of five. It is characterized by fever and inflammation of small to medium-sized arteries. This case report presents the case of a nine-year-old boy with KD who developed Kawasaki disease shock syndrome (KDSS) complicated by bilateral pleural effusion, which is a rare occurrence. KDSS is defined as KD accompanied by low blood pressure or signs of inadequate blood flow, leading to increased cardiovascular complications. The patient exhibited typical KD symptoms, including conjunctivitis, mucosal changes, rash, extremity swelling, and lymphadenopathy...
November 2023: Curēus
https://read.qxmd.com/read/38155741/tumor-necrosis-factor-receptor-associated-cycle-syndrome-a-case-report-and-literature-review
#37
Ziwei Li, Xiaoping Jing, Shuya Zhang, Tiantian Liu, Qingyin Guo
Recurring episodes of fever characterize tumor necrosis factor receptor-associated periodic syndrome (TRAPS) which is autosomal dominant. The primary symptoms of patients with TRAPS include prolonged fever, abdominal pain, muscle pain, and skin rashes. The prevalence of TRAPS appeared higher in Western countries than in Asian countries. Herein, we present the case of a 13-year-old girl who experienced intermittent fever for 8 years, with episodes that occur every 2 years. The patient demonstrated periodic fever, headache, vomiting, rash, and elevated inflammatory marker levels during the disease course...
2023: Frontiers in Pediatrics
https://read.qxmd.com/read/38154979/-analysis-of-9-cases-of-drug-induced-hypersensitivity-syndrome-related-hemophagocytic-lymphohistiocytosis
#38
JOURNAL ARTICLE
Y Z Zhao, H H Ma, D Wang, H Y Lian, T Y Wang, R Zhang
Objective: To analyze the clinical features,treatment and prognosis of drug induced hypersensitivity syndrome related hemophagocytic lymphohistiocytosis (DIHS-HLH). Methods: This was a retrospective case study. Clinical characteristics, laboratory results, treatment and prognosis of 9 patients diagnosed with DIHS-HLH in Beijing Children's hospital between January 2020 and December 2022 were summarized. Kaplan-Meier survival analysis was used to calculate the overall survival rate. Results: Among all 9 cases, there were 6 males and 3 females, with the age ranged from 0...
January 2, 2024: Zhonghua Er Ke za Zhi. Chinese Journal of Pediatrics
https://read.qxmd.com/read/38154978/-clinical-analysis-of-11-cases-multisystem-inflammatory-syndrome-associated-with-sars-cov-2-omicron-variant-infection-in-children
#39
JOURNAL ARTICLE
H S Zhang, X T Chang, P H Wu, D Y Song, G Ge, W Ding, Z W Hu, G F Wang, Y W Jiang, L P Ye
Objective: To explore the clinical characteristics, diagnosis, treatment, and follow-up of multisystem inflammatory syndrome in children (MIS-C) related to SARS-CoV-2 Omicron variant infection. Methods: A retrospective analysis was conducted on clinical data of 11 children with MIS-C, who were admitted to the Department of Pediatrics of Peking University First Hospital from December 2022 to January 2023. Clinical characteristics, treatment, and follow-up of MIS-C were summarized in this study. Results: The 11 cases contained 7 boys and 4 girls, with an age of 4...
January 2, 2024: Zhonghua Er Ke za Zhi. Chinese Journal of Pediatrics
https://read.qxmd.com/read/38140542/monkeypox-virus-immune-evasion-and-eye-manifestation-beyond-eyelid-implications
#40
REVIEW
Francisco D Lucena-Neto, Luiz F M Falcão, Adolfo S Vieira-Junior, Evelly C S Moraes, Joacy P F David, Camilla C Silva, Jorge R Sousa, Maria I S Duarte, Pedro F C Vasconcelos, Juarez A S Quaresma
Monkeypox virus (MPXV), belonging to the Poxviridae family and Orthopoxvirus genus, is closely related to the smallpox virus. Initial prodromal symptoms typically include headache, fever, and lymphadenopathy. This review aims to detail various ocular manifestations and immune evasion associated with the monkeypox viral infection and its complications, making it appropriate as a narrative review. Common external ocular manifestations of MPXV typically involve a generalized pustular rash, keratitis, discharges, and dried secretions related to conjunctival pustules, photophobia, and lacrimation...
November 23, 2023: Viruses
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