Since 1932, Harvey Cushing first proposed pituitary adenoma as the cause of acromegaly. The disease is recognised as a benign tumour, which can be easily cured or controlled by conventional therapies, including surgery, radiotherapy and/or medical treatment.
A large proportion of the cases, which are identified incidentally and exhibit no symptoms, do not require any treatment. In these cases, periodic surveillance is the only medical measure required. Other than pituitary carcinoma (metastatic PitNET), only a very small subset of pituitary adenomas present aggressively in nature, which means rapid growth rate and being refractory to optimised standard treatment.
In the cancer definition, any malignant tumour must be positively diagnosed with histological confirmation.
In cases where no clinical treatment is required, or non-invasive treatment is the only medical measure to take, these tumours will not be diagnosed through histological methods.
A key point is that whilst being reclassified by WHO as malignant, these tumours exhibit variable growth patterns across a spectrum of malignant behaviour, with the vast majority exhibiting indolent and non-aggressive behaviour.
The change by WHO from benign to malignant is not representing a new disease process, it is a nomenclature change, a reclassification of previously considered benign adenoma to overt malignancy. The WHO reclassification will not influence the associated risk or clinical pathway because the diagnostic label has been amended. These are the same (previously labelled) adenomas brought into line under one new heading.
Therefore pituitary tumours without histological proof, or the necessity of specific cancer treatment such as surgery or radiation therapy, are beyond the scope of cancer coverage that CI policy reasonably intends to pay.
We would advise that any particularly unusual or ‘grey’ claims are referred to Pacific Life Re for opinion.