Neuroendocrine tumour of The Lung (Lung NETs) are a rare and unusual form of lung cancer that originates in neuroendocrine cells—specialised lung cells that help regulate key body functions by releasing hormones. These tumours can vary significantly in behaviour. Some...
Muir–Torre Syndrome (MTS) is a rare, inherited condition that increases the risk of certain skin and internal cancers—most notably colorectal cancer. It is considered a variant of Lynch syndrome (hereditary nonpolyposis colorectal cancer or HNPCC), a genetic disorder...
Pleuropulmonary blastoma (PPB) is a rare but aggressive type of cancer that occurs in early childhood. It develops in the lungs or the pleura—the thin layer of tissue lining the lungs. PPB most often affects children under the age of six. Tumours can present in...
Medulloepithelioma of the eye is a rare tumour that develops from the non-pigmented ciliary epithelium, the tissue responsible for producing the fluid inside the eye. It most often occurs in young children, typically under the age of 10. This tumour closely...
Carney’s Triad Tumour is a rare, non-hereditary condition characterised by the occurrence of three types of tumours: Gastrointestinal Stromal tumours (GISTs): Cancers that arise in the digestive tract, most commonly the stomach or small intestine. Pulmonary...
