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 ...

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

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 ...

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, ...

Figure 3 (A) H&E, 10×—mild to moderate spongiosis with dense perivascular and periadnexal infiltrate in the superficial and deep dermis. (B) H&E, 40×—the infiltrates consist mainly of neutrophils with ...

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 ...

Description 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, ...

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 ...