We present a case of a female in her late 40s with a 5-year history of well-managed type II diabetes mellitus, systemic hypertension and dyslipidaemia presented with acute severe abdominal pain, ...

In this report, we present an adolescent patient with a 46,XY karyotype and phenotypically female genitalia secondary to campomelic dysplasia who presented with primary amenorrhea. This patient is ...

The spread of acute myeloid leukaemia (AML) outside of the blood or bone marrow is known as extramedullary involvement, and common sites include the skin, bone and lymph nodes. Here, we describe a ...

Anti-α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor limbic encephalitis is a rare neurological disorder often associated with malignancies. We present the case of a patient in ...

Pseudohypertrophy of muscles is a rare and under-recognised form of hypothyroid myopathy primarily affecting the calf muscles, in association with elevated muscle enzymes. We report the case of an ...

Topical steroid withdrawal (TSW) is a serious and often under-recognised dermatological condition. It is an adverse reaction to prolonged use of topical corticosteroids (TCS), which may occur ...

Tumour necrosis factor alpha (TNF-α) inhibitors are licensed for use in autoimmune conditions such as psoriasis, and there have been reported cases of liver injury associated with infliximab and ...

A male in his 50s presented to the renal department with a diagnostic challenge of an unexplained kidney injury.

Crossed fused renal ectopia (CFRE) is an uncommon and congenital anomaly in which both kidneys are fused and located on one side of the body, often going undetected due to its asymptomatic nature.

Primary intestinal lymphangiectasia (PIL) is a rare cause of lymphatic dysfunction leading to enteric protein loss in children. This case report describes a male child, with familial short stature who ...

Extracorporeal membrane oxygenation (ECMO) technology has relative contraindications in haemorrhagic disease but remains an effective therapeutic option for the treatment of pulmonary haemorrhage ...

Maturity-onset diabetes of the young (MODY) is an autosomal dominant monogenic form of diabetes. This report describes a case with hepatocyte nuclear factor 1-alpha ( HNF1A )-MODY due to a novel ...