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Pancreatic neuroendocrine tumours–a rare pancreatic tumour
David L Chan Nick Pavlakis Paul Roach Dale Bailey Jennifer Arena Eva Segelov
2017/2/22
Pancreatic neuroendocrine tumours are rare tumours that can either present with syndromes from excess hormonal production or from mass effect – from the primary or metastases. They vary widely in clin...
Genomics of pancreatic tumours-what we now know
Pancreatic cancer tumor complex landscape pancreatic cancer genome
2017/2/22
Each year, over 2500 patients in Australia are diagnosed with pancreatic cancer. Pancreatic cancer is one of the most lethal tumour types with a five year survival of just 5%, thus there is a need to ...
Rare molecular subsets among lung tumours–what makes them stand apart from the common?
Rare molecular subsets tumours cancers
2015/4/21
While there is no universally agreed upon definition, rare malignancies are often defined as those with an incidence of <6 per l00,000 population. However, increasingly, commonly occurring cancers are...
Brain tumours: Successes and challenges on the other side of the blood-brain barrier
Brain tumours the blood-brain barrier cancers
2015/4/21
Tumours of the central nervous system encompass a large variety of cancers, ranging from slow-growing to rapidly progressive. Although comparatively rare in adults, central nervous system malignancies...
Rare urogenital tumours likely to be encountered by oncologists include testicular cancer, non-urothelial tumours of the bladder and urethral and penile cancers. Testicular cancer is a rare but highly...
Neuroendocrine tumours–models for rare tumour management
Neuroendocrine tumours rare tumour management
2015/4/21
Neuroendocrine tumours have posed a challenge for the development of research and management strategies because of their rarity and heterogeneity, both from clinical and molecular perspectives. Classi...
Childhood solid tumours occurring in adolescents and young adults
Childhood solid tumours adolescents and young adults
2015/3/27
A small number of adolescents and young adults are diagnosed with solid tumours that typically occur in childhood – the most common are neuroblastoma, Wilms’ tumour and rhabdomyosarcoma. In general, ...
Brachial plexus surgery and apical lung tumours
Brachial plexus surgery apical lung tumours
2015/3/17
Historically, management of apical lung tumours (superior sulcus tumours or Pancoast tumours) that involve the brachial plexus has been very limited, and usually all that was offered was palliative ca...
Australian Neuroendocrine Tumours (NETs) Consensus Workshop Report
Australian Neuroendocrine Tumours Consensus Workshop Report
2015/1/23
Neuroendocrine tumours (NETs) are a rare group of heterogeneous neoplasms arising from
the diffuse neuroendocrine system of the gastrointestinal tract or bronchopulmonary system.
The annual incide...
A team of researchers has pinpointed a handful of genes that could drive the formation of medulloblastoma, the most aggressive and frequent form of brain tumour found in children.
Researchers delve into genetic code of tumours in hunt for cancer therapies
genetic code of tumours cancer therapies
2010/4/29
Australian scientists are playing a vital role in a worldwide search for cancer therapies, described in the top scientific journal Nature overnight (15th April). The scientists are part of the Interna...
Concurrent development of testicular seminoma and choriocarcinoma of the superior mediastinum, presented as cervical mass: a case report and implications about pathogenesis of germ-cell tumours
germ cell tumours histology genetic
2006/11/23
20 November 2006，Synchronous presentation of more than one germ cell tumours of different histology in the same patient is considered to be very rare. In these cases of multiple germ cell tumours, str...