Plasmacytomas are rare monoclonal plasma cell neoplasms, with extramedullary involvement being uncommon. Pancreatic plasmacytoma is exceedingly rare, and dual-site involvement remains poorly documented.
Pancreatic Neuroendocrine Tumours (PanNETs) are uncommon neoplasms, and constitute a small fraction of pancreatic neoplasms yet remain clinically important within the spectrum of Gastroenteropancreatic Neuroendocrine Neoplasms (GEP-NEN).
Abusive Head Trauma (AHT) in infants often presents with distinctive ocular findings, most notably Retinal Hemorrhages (RH) [1]. RH are a hallmark sign of AHT – found in roughly 85% of diagnosed cases –whereas such extensive hemorrhages are rarely seen in accidental injuries or other medical conditions [2,3].
Diagnosing rare conditions can often be clouded by atypical symptoms that mislead clinicians, delaying accurate identification and treatment. Ocular Myasthenia Gravis (OMG) exemplifies this diagnostic challenge, presenting with hallmark symptoms such as ptosis, diplopia, and ophthalmoplegia.
A 20-year-old male presented with unexplained left upper abdominal pain persisting for over one month. He had been diagnosed with Acute Myeloid Leukemia (AML) one month prior, experiencing two episodes of high-grade fever (Tmax >39°C) before achieving remission through induction chemotherapy.
A 61-year-old Chinese lady with a background of a previous spinal cord tumour presented to the Emergency Department with severe pneumonia requiring ventilatory support. On examination, multiple eruptive seborrheic keratoses which had suddenly developed 3 years ago were incidentally noted over her back.
Late hemothorax is a rare but potentially life-treathening complication of penetrating thoracic injuries and pseudoaneurysm of the intercostal arteries is one of the rarest causes for this condition. Pseudoaneurysms may remain asymptomatic for a long time.
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