Anti-N-methyl-D-aspartate (NMDA) encephalitis is marked by rapidly evolving and severe neuropsychiatric symptoms that can affect any age. This case illustrates a woman in her early 40s who was ...

Müllerian duct cysts are rare congenital anomalies arising from persistent remnants of the paramesonephric (Müllerian) duct system. The coexistence of Müllerian duct cysts with prostate adenocarcinoma ...

Fontan physiology poses unique anaesthetic challenges due to passive pulmonary circulation, preload dependence and elevated ...

Paediatric orbital tumours are rare, and primary orbital lymphomas are particularly uncommon, with an incidence of approximately 0.12 per 1000 000 children. Such lymphomas may present as orbital ...

This case report describes a woman in her 60s diagnosed with primary vitreoretinal lymphoma (PVRL) with leptomeningeal ...

Occipital meningomyeloceles are rare and challenging conditions for the anaesthesiologist, mainly because of the difficulty ...

Congenital duodenal obstruction (CDO) is a recognised anomaly frequently associated with Down syndrome (DS). While complete obstruction is typically diagnosed in the neonatal period, incomplete ...

Standard airway management in deteriorating super morbidly obese patients can lead to cardiovascular collapse because of their poor physiological reserves. In this report, we describe a case of awake ...

We present a case of a postmenopausal woman with androgenic alopecia and very high testosterone levels of 16 nmol/L (normal ...

We report a rare case of Cushing’s syndrome in a pregnant woman carrying twins. Interestingly, the patient did exhibit many of the classic clinical features typically associated with hypercortisolism, ...

Progressive multifocal leukoencephalopathy (PML), caused by reactivation of JC virus, typically develops in individuals with profound immunosuppression, but may also occur in those with more subtle ...

Narcolepsy is a rare disorder of central hypersomnolence which is often under-recognised owing to a variable clinical phenotype. Narcolepsy type 1 (NT1) is caused by loss of hypothalamic hypocretin ...