Background: Necrotizing fasciitis is a rapidly progressive, life-threatening soft tissue infection associated with high morbidity and mortality, particularly in patients with diabetes and other comorbidities. Case Presentation: We report a 61-year-old woman with poorly controlled...
Open access
Research Article10.9734/ajcrmh/2026/v9i1320
Juvenile systemic lupus erythematosus (JSLE) is a rare but aggressive autoimmune disease in children, with boys comprising only 10–20% of cases. Cutaneous manifestations are often the initial or predominant feature, yet atypical palmar-plantar lesions and flares triggered by medi...
Open access
Research Article10.9734/ajrimps/2026/v15i2385
Rasmussen’s encephalitis (RE) is a rare, chronic, progressive inflammatory neurological disorder that causes unilateral hemispheric inflammation, drug-resistant focal seizures, and progressive neurological deficits. It mainly affects children and often mimics other forms of refra...
Open access
Research Article10.9734/ajcrmh/2026/v9i1312
Spindle cell carcinoma is a rare, aggressive biphasic variant of squamous cell carcinoma with exceptionally low incidence in the shoulder region. We describe a 25-year-old male who developed isolated left upper limb weakness and complete sensory loss immediately after surgical ex...
Open access
Research Article10.9734/ajmpcp/2026/v9i1417
Background: Hoffmann’s syndrome is a rare and underdiagnosed form of hypothyroid myopathy that can closely mimic autoimmune inflammatory myopathies such as polymyositis, potentially leading to inappropriate immunosuppressive therapy. Case Presentation: A 39-year-old female with i...
Open access
Research Article10.9734/ajcrmh/2026/v9i1311