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Sub-Lingual Implantation Keratinized Epidermoid Cyst Masquerading as Plunging Ranula: Report of a Rare Case with Literature Review.
Indian J Otolaryngol Head Neck Surg
January 2025
Basaveshwara Medical College & Hospital, Chitradurga, Karnataka 577501 India.
Sublingual epidermoid cysts are rare benign lesions derived from ectodermal tissue, typically located beneath the tongue or the floor of the mouth. While often asymptomatic, these cysts can grow and cause discomfort or complications, making accurate diagnosis and appropriate treatment crucial. We present the case of a 6-year-old Indian girl diagnosed with an implantation keratinized sublingual epidermoid cyst, initially misidentified as a plunging ranula.
View Article and Find Full Text PDFAseptic meningitis in the setting of giant cell arteritis (GCA): a case report.
BMC Rheumatol
March 2025
Department of Medicine, Albury-Wodonga Health, Albury, NSW, Australia.
Background: Giant cell arteritis (GCA) is a vasculitis primarily affecting medium- and large-sized arteries. The diagnosis may be challenging and lead to delays in treatment. Cerebrospinal fluid (CSF) pleocytosis is an uncommon association but may occur due to central nervous system (CNS) vasculitis or pachymeningitis.
View Article and Find Full Text PDFMetastatic olfactory neuroblastoma with unusual solitary metastasis to femur: a case report and literature review.
World J Surg Oncol
March 2025
Department of Orthopedic Surgery, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Background: Olfactory neuroblastoma (ONB) is a rare malignancy that develops in the nasal cavity, with appendicular skeletal metastases being exceptionally uncommon. We report the case of a middle-aged male with ONB, presenting with an unusual biopsy-confirmed solitary metastasis to the left proximal femur.
Case Presentation: A 33-year-old male was previously diagnosed with olfactory neuroblastoma in the skull base after initial clinical presentation with progressive left-sided nasal obstruction for six months.
Purpose: We describe a case of bilateral, multiple, branch retinal artery occlusions (BRAO) associated with carotid webs.
Methods: A thorough chart review was conducted for the patient. Relevant literature was systematically reviewed.
A Rare Case of Postpartum Portal Vein Thrombosis in a Young Patient With Heterozygous Prothrombin G20210A Mutation.
Cureus
February 2025
Internal Medicine, Lebanese University Faculty of Medical Sciences, Beirut, LBN.
Portal vein thrombosis (PVT) is most commonly associated with cirrhosis due to the reduced blood flow through the liver. However, its occurrence in non-cirrhotic individuals is rare and typically linked to hypercoagulable states. The postpartum period is a recognized hypercoagulable state, yet PVT in this context remains uncommon.
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