Hereditary angioedema (HAE) is a genetic disorder that causes sudden episodes of swelling, often accompanied by abdominal pain. Affecting roughly 1 in 50 000 people, HAE typically appears in childhood ...

A woman in her 40s with a history of a subarachnoid haemorrhage complicated by ischaemic infarcts presented with 1 week of ...

Neurofibromatosis Type 1 (NF1) is a genetic disorder characterised by benign tumours and cutaneous lesions, including neurofibromas. This case report describes a boy in his early 10s with NF1 who ...

Perianal Paget’s disease (PPD) is a rare condition which is often associated with underlying malignancy. To definitively rule ...

Patients with inoperable hepatobiliary cancers often endure severe abdominal pain, which impacts their quality of life. This pain is usually a combination of both nociceptive and neuropathic pain, ...

An adult male patient, a known case of ALCL (anaplastic large cell lymphoma-T-cell) since the last 1 month, presented to dermatology OPD with sudden onset of multiple, painful, reddish and raised ...

Multiple myeloma is a rare haematologic malignancy, representing about 1–2% of all cancers and 17% of haematologic malignancies in the US, predominantly affecting older adults and more common in ...

Neonicotinoid is a new class of systemic insecticides that are selectively toxic to insects. However, cases of human toxicity have been reported. A man in his 60s, who worked as a pest control ...

A man in his early 70s was admitted to our hospital with uncontrollable bilateral arm movements that had started 2 days prior to the presentation. He had a negative history of chorea, diabetes ...

Macrocheilia, or lip enlargement, has a varied aetiology, but granulomatous conditions, both infective and non-infective, comprise a significant proportion of patients. Diagnosis starts with clinical ...

Langerhans cell histiocytosis (LCH) is a neoplastic disease characterised by the deposition of granulomatous lesions in various tissues in the body. LCH of the lateral skull base commonly presents ...

Relapsing polychondritis is a rare autoimmune-driven cause of cartilaginous inflammation with multi-systemic impact and disease. We present an acute presentation of optic neuropathy on an eight-month ...