A young woman (G4P2L0A1) diagnosed with a case of Takayasu arteritis (Type IV) and a history of recurrent pregnancy loss presented at 7 weeks of gestation with chronic hypertension. She was on ...
Immune checkpoint inhibitor (ICI) pneumonitis is a potentially life-threatening immune-related adverse event associated with ICI therapy across various malignancies. ICIs enhance antitumour immunity ...
A female patient in the 70s presented with bilateral flank pain and haematuria. Evaluation confirmed tuberous sclerosis complex (TSC) with cutaneous findings, a giant renal angiomyolipoma (AML) in the ...
We present the youngest reported case of an intracranial arterial pseudoaneurysm in a newborn following a difficult delivery. The infant presented with multicompartment intracranial haemorrhage and ...
A female patient in her 70s with a remote history of vocal cord paralysis was incidentally found to have a pulmonary artery aneurysm on a chest CT. Serial imaging performed over 3 years noted ...
Hepatopulmonary syndrome (HPS) is an under-recognised complication of chronic liver disease, affecting 10%–30% of patients with cirrhosis. It involves intrapulmonary vascular dilatations, arterial ...
The use of synthetic mesh in the abdominal compartment has recently become a topic of debate as high profile public cases have called into question their safety. Several case reports have demonstrated ...
Spontaneous haemoperitoneum is described as a collection of blood in the peritoneal cavity due to non-traumatic aetiology. Common causes in the literature include splenic, hepatic and gynaecological ...
A 61-year-old Caucasian woman presented to the emergency room complaining of left-sided chest pain and altered mentation for 3 days. Her medical history included liver cirrhosis and coronary artery ...
1 Department of Neurology, University of Utah, Salt Lake City, Utah, USA 2 Department of Pharmacy Services, University of Utah, Salt Lake City, Utah, USA Cyclobenzaprine is commonly used as a muscle ...
We report a rare case of acute neurological Behçet’s disease (neuro-BD) diagnosed concurrently with systemic Behçet’s disease ...
Atypical presentation of biotinidase deficiency: masquerading neuromyelitis optica spectrum disorder
Biotinidase deficiency (BTD) is a treatable, inherited metabolic disorder commonly characterised by alopecia, dermatitis, seizures and developmental delay. It can also manifest as optic neuritis and ...
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