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H syndrome with bilateral choroidal osteoma: Coincidence or association?
Eur J Ophthalmol
January 2025
Department of Medical Genetics, Istanbul Medipol University, Istanbul, Turkey.
Purpose: To report a case with bilateral corneal arcus and bilateral choroidal osteoma associated with H syndrome.
Methods: Descriptive case report.
Results: A 16-year-old girl with H syndrome was followed up in the pediatric nephrology clinic for chronic renal failure and was consulted to the ophthalmology clinic.
FDG PET/CT in a Case of Gardner Syndrome.
Clin Nucl Med
December 2024
From the Department of Neurology, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine.
Gardner syndrome is characterized by multiple intestinal polyps and extraintestinal lesions. We describe FDG PET/CT findings of the extraintestinal lesions in a patient with Gardner syndrome. FDG PET/CT showed 2 hypermetabolic desmoid tumors in the abdominal wall, sclerotic areas with multifocal activity in the maxilla and mandible, multiple osteomas in the bilateral parietal, left frontal, sphenoid and ethmoid bones, an impacted tooth in the right maxilla, and bone islands in the T2 and T5 vertebral bodies.
View Article and Find Full Text PDFPost-traumatic extensive chronic osteomyelitis of skull vault: An illustrative case report.
Pak J Med Sci
December 2024
Ahtesham Khizar, MBBS, FCPS (Neurosurgery), Department of Neurosurgery Unit-I, Punjab Institute of Neurosciences, Lahore, Pakistan.
Chronic osteomyelitis of the skull base is a commonly reported pathology in existing scientific literature, but chronic osteomyelitis of the skull vault (COSV) is a rarely documented disease. We report the case of a 38 years old Afghan male with a presenting complaint of irregular swelling on the skull vault for six months. The patient had a history of head trauma one year back with a compound depressed fracture which had been surgically managed then.
View Article and Find Full Text PDFInhibition of choroidal osteoma progression using bisphosphonate and RANKL-inhibitory treatment.
Am J Ophthalmol Case Rep
December 2024
Department of Ophthalmology, University of California, San Francisco, San Francisco, USA.
Purpose: To describe the use of anti-osteoclastic medications (i.e., bisphosphonates and receptor activator of nuclear factor kappa beta (RANK) ligand inhibitors) in treating choroidal osteoma.
View Article and Find Full Text PDFSynchronous cemento-ossifying fibromas: a systematic review.
Med Oral Patol Oral Cir Bucal
September 2024
Universidade Federal do Rio Grande do Sul Faculdade de Odontologia, Rua Ramiro Barcelos, 2492, sala 503 CEP: 90035-003, Santana, Porto Alegre RS, Brazil
Article Synopsis
- - This systematic review analyzed published data on synchronous cemento-ossifying fibromas (COF), including their demographic and clinical features, utilizing various databases and following PRISMA guidelines.
- - A total of 19 studies with 20 COF cases were examined, revealing a mean patient age of 35 years, a predominance of female patients (60%), and simultaneous involvement of the mandible and maxilla in 65% of cases.
- - Management typically involved surgical procedures, with a recurrence rate noted in 15% of cases that had follow-ups, and the findings suggest that synchronous COF is rare, especially affecting women in their 30s.
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