Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
A Rare Case of Salmonella Enteritidis Sinusitis.
Cureus
December 2024
Infectious Disease, Tan Tock Seng Hospital, Singapore, SGP.
Nontyphoidal is a common cause of gastroenteritis but can also lead to bacteremia and extraintestinal infections, including meningitis (more frequent in children and infants), endovascular infections (e.g., endocarditis and infected aneurysms), urinary tract infections, and bone or bone marrow infections (e.
View Article and Find Full Text PDFChallenges in diagnosis and management of Langerhans Cell Histiocytosis in a 13-month-old child: a rare case report.
Ann Med Surg (Lond)
September 2024
Department of Pathology, Institute of Medicine, Tribhuvan University Teaching Hospital, Kathmandu, Nepal.
Article Synopsis
- Langerhans Cell Histiocytosis (LCH) is a rare pediatric condition caused by an excessive number of abnormal Langerhans cells, typically affecting children aged 1 to 3 and can involve various organs, notably the skeleton and skin.
- A case study details a 13-month-old boy presenting with fever, rash, and swelling, diagnosed through imaging and a biopsy, resulting in treatment with vinblastine and prednisolone that improved his condition.
- LCH can manifest in different ways and requires careful diagnosis and treatment based on how widespread the disease is, emphasizing the importance of considering it in cases of ongoing skin and bone issues in children for effective management.*
Three-dimensional computer navigation in the reconstruction of complex unilateral orbital fractures: evaluation and review of applications.
Arch Craniofac Surg
August 2024
Department of Plastic Surgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Background: The eyes are the central aesthetic unit of the face. Maxillofacial trauma can alter facial proportions and affect visual function with varying degrees of severity. Conventional approaches to reconstruction have numerous limitations, making the process challenging.
View Article and Find Full Text PDFBeckwith-Wiedemann Syndrome With Severe Relapsing Hypoglycemia After the Neonatal Period: A Case Report and a Literature Review.
Cureus
April 2024
Pediatrics, King Fahd Military Medical Complex, Dhahran, SAU.
Beckwith-Wiedemann syndrome (BWS) is a rare genomic imprinting disorder that affects multiple systems. Major features can manifest as large birth weight, anterior abdominal wall defects, macroglossia, hyperinsulinism, organomegaly hemihypertrophy, and renal abnormalities. Characteristic facies manifested as midface hypoplasia, infraorbital creases, facial nevus simplex, and anterior linear ear lobe creases/posterior helical ear pits, with a predisposition to tumor development.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!