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682 articles
September 202624
Large vessel occlusion stroke in venom-induced consumption coagulopathy after viper envenomation.
A woman in her mid-60s presented with left-sided hemiplegia 6 hours post-viper bite. Investigations revealed profound venom-induced consumption coagulopathy and an acute right middle cerebral artery occlusion.
Post-streptococcal uveitis syndrome in a middle-aged adult patient.
A 53-year-old woman developed bilateral panuveitis after a documented case of streptococcal pharyngitis. She presented with photophobia, blurred vision, and floaters.
Multiple hepatic artery pseudoaneurysms associated with visceral larva migrans: a rare cause of upper gastrointestinal bleeding in a child.
A 3-year-old girl presented with prolonged fever, abdominal pain, and haematemesis. Laboratory tests revealed anaemia, elevated eosinophils, jaundice, high serum IgE, and positive Toxocara serology.
Total knee arthroplasty in Brown-Séquard syndrome.
A patient with Brown-Séquard syndrome presented with severe neuropathic pain due to osteoarthritis. After conservative treatments failed, total knee arthroplasty was performed.
Complicated allergic fungal rhinosinusitis: diagnostic complexities and management strategies.
A man in his 60s presented with diplopia, headache, and facial numbness, leading to a diagnosis of bilateral abducens nerve palsy and partial right third nerve palsy.
Systemic light chain amyloidosis presenting as jejunal perforation.
A patient with recurrent uterine cancer presented with jejunal perforation, a rare complication of systemic light chain amyloidosis.
Posterior chamber phakic intraocular lens in posterior polymorphous corneal dystrophy.
A woman in her early 20s with bilateral compound myopic astigmatism and unilateral posterior polymorphous corneal dystrophy (PPCD) underwent sequential bilateral implantation of toric posterior chamber phakic…
PCR-Confirmed Convexity Subarachnoid Neurocysticercosis with Negative Serology: A Case Report.
A patient with a six-month history of focal seizures was diagnosed with convexity subarachnoid neurocysticercosis after surgical excision of a cystic lesion.
A case report of sporadic Creutzfeldt-Jakob disease presenting with progressive opsoclonus-myoclonus-ataxia-Plus (OMAS-Plus) phenotype.
A 63-year-old man presented with progressive dysarthria and bulbar symptoms, initially suggestive of myasthenia gravis. His condition deteriorated, leading to right-predominant hemiataxia, polymyoclonus, and cognitive…
Discordant pathologic response to neoadjuvant human epidermal growth factor receptor 2-directed therapy in primary breast tumour and axillary lymph node metastases.
A patient with HER2-positive breast cancer received neoadjuvant chemotherapy and HER2-directed therapy, showing significant histological response in the primary breast tumor.
Staged embolisation strategy for spinal epidural arteriovenous fistula with concomitant pulmonary arteriovenous malformation.
An elderly woman presented with progressive paraparesis due to a suspected spinal arteriovenous shunt. During her hospitalization, she experienced multiterritory embolic stroke, leading to the discovery of bilateral…
Recurrent breast abscess leading to an incidental diagnosis of tuberculous mastitis: a case report.
A 26-year-old Indian woman presented with a recurrent right breast abscess characterized by a tender, fluctuant swelling. Initial management included incision and drainage.
Treatment of bilateral Irvine-Gass syndrome with suprachoroidal triamcinolone injection.
A woman in her 60s developed bilateral cystoid macular oedema (CME) following sequential cataract surgeries, resulting in a decline in visual acuity.
Immunoglobulin A-dominant crescentic glomerulonephritis in a teenage refugee with active methicillin-resistant Staphylococcus aureus urinary infection: a diagnostic and therapeutic dilemma.
A teenage refugee presented with rapidly progressive renal failure, nephrotic-range proteinuria, and fluid overload necessitating haemodialysis.
Heterotopic prostatic tissue mimicking prostate cancer: the decisive role of multiparametric MRI.
A man in his 70s was referred for urological evaluation because of a progressive increase in serum prostate-specific antigen levels.
Pneumoperitoneum following revision hip arthroplasty without hollow viscus perforation: a gastrointestinal surgical diagnostic challenge and the importance of clinical-radiological correlation.
A woman in her 50s developed pneumoperitoneum after revision hip arthroplasty for prosthetic joint infection. Despite elevated inflammatory markers, her abdomen was soft and non-tender.
Sesamoid non-union treatment using suture anchor fixation.
A woman in her 20s presented with a 3-year history of intermittent plantar pain beneath the first metatarsal head and instability of the first metatarsophalangeal joint.
Asynchronous bilateral pulmonary pathology: left-sided congenital pulmonary airway malformation with contralateral malignant pleuropulmonary blastoma in an adolescent.
An adolescent boy with a history of left-sided congenital pulmonary airway malformation (CPAM) presented with dry cough, right-sided chest pain, and breathlessness.
Pure Motor Axonal Neuropathy Associated with Sjögren's Syndrome: A Rare Case Report.
A 47-year-old man with a history of sicca symptoms presented with progressive, asymmetric motor weakness in all four limbs, without sensory involvement.
Eisenmenger Syndrome After Delayed Atrial Septal Defect Closure at High Altitude: A Case Report.
A 46-year-old woman presented with severe cyanosis and heart failure 22 years after atrial septal defect closure, living at high altitude in the Ecuadorian Andes.
Extraosseous Ewing sarcoma of the common fibular nerve.
A 64-year-old woman presented with progressive weakness of the left foot, leading to the diagnosis of an intraneural extraosseous Ewing sarcoma of the common fibular nerve.
Coma from severe spontaneous intracranial hypotension due to a CSF-venous fistula.
A patient presented in a coma due to severe spontaneous intracranial hypotension (SIH) caused by a spinal CSF-venous fistula. The condition led to significant brain sagging, compromising brainstem function.
Arthrogryposis as a neuromuscular phenotype: lessons from PIEZO2 loss-of-function.
A 43-year-old woman presented with congenital clubfoot, progressive scoliosis, and distal joint contractures. Neurological examination revealed pure sensory findings, global areflexia, severe sensory ataxia, and a…
Hereditary transthyretin amyloidosis with hand weakness and bulbar involvement.
A 76-year-old man presented with progressive motor weakness, bulbar symptoms, and hand muscle atrophy, initially misdiagnosed as motor neurone disease.
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