Pituitary Surgery Tumours vary in size and activity. If surgery is recommended it may be for one of three reasons:
- to remove hormone-producing tissue (typically in Acromegaly or Cushing's disease)
- to reduce the volume of a tumour that is compressing the optic chiasm or other structures
- to reduce the volume of, or excise, non hormone-producing tissue that is likely to threaten surrounding structures in the future; for example, in a relatively young patient, in whom continued growth of the tumour is suspected or has been proven by sequential scans.
Transsphenoidal surgery is the most usual method but sometimes transcranial surgery is required in some tumours with major intracranial extension. The transsphenoidal approach allows the surgeon a clear, direct view of the tumour (through an operating microscope) and avoids a craniotomy (making a hole in the skull) with its associated risks of damage to the brain and epilepsy. Recently an endoscopic approach has been introduced in some centres. Fine tubes (endoscopes) are pushed through the back of the nose. MRI and/or CT scans will give the surgeon information on the size and position of the tumour. Successful outcome of this surgery is very dependent on the experience of the surgeon. Patient managementPrior to SurgeryThe Pituitary Foundation recommends that the initial point of referral is to an Endocrinologist who will arrange for essential preliminary tests (including blood tests, MRI and visual fields) to be performed before surgery. Follow-upThe patient will be referred to an endocrinologist for post-operative pituitary function assessment at about 5-8 weeks and back to the surgeon at about 12 weeks (for MRI and visual field assessment). In some cases additional replacement pituitary hormones will be needed. These appointments should, ideally, be combined to cause minimal inconvenience to the patient. If the patient suffers from new onset polyuria and nocturia after surgery, it is likely that they have developed a degree of diabetes insipidus (DI). This is unusual after transsphenoidal surgery, but in all cases is highly amenable to treatment. In most cases, DI is temporary and disappears within a few months, but in 1-2% of patients, especially after removal of Prolactinoma and Cushing's tumours, it may be permanent and remain treatable. It is possible to develop a CSF leak from the nose in the post-operative period (this is rare). This is associated with a risk of meningitis, and is an inconvience for the patient. Any flu-like symptoms or discharge of water-like fluid from the nose should be treated with a view to this posibility. Patients need to be referred back to the surgeon for treatment urgently. SinusitisThis is not uncommon after this operation, particularly for patients with acromegaly. Symptoms usually clear given time, but occasionally need further treatment or an ENT referral. StitchesDepending on the surgical technique, stitches are inserted in the upper gum or in the nostril. They are usually soluble. The wound itself will be completely healed in 3 weeks. Complete absorption of stitches can take 3 months and loose ends may need to be removed/snipped away. There may be some numbness around the front teeth; this may occasionally be permanent. Weight gainA major problem for many patients is weight gain. These patients are likely to need some encouragement to follow a suitable diet and take regular exercise. This may be particularly difficult after a period of illness and hospitalisation. However, including more exercise into their lifestyle should also improve the patient's general feeling of well-being. Emotional impactSurgical treatment which involves the head has a strong emotional impact for some patients. Please see 'Psychological Issues' (factsheet 13). Questions patients may askWhy do I need an operation? A Benign tumour of the Pituitary gland may be compressing the optic nerve (which lies just above it) and is affecting your sight or you may have a tumour which is producing excessive amounts of hormone which could cause you problems. Is it cancer? No, the vast majority of tumours are benign. How long with I be in hospital? This varies between treatment centres, but may be 3-9 days. When will I be able to go back to work? Depending on the job and circumstances, it is usually wise to plan for about 4-6 weeks off and reassess after that time. Some patients may take longer to recover (factsheet 13). Have I inherited this, will my children get it? In all but very exceptional circumstances there is no hereditary link. Resources for patientsPlease go to the Resource Library of this website to access resources for patients. Our library includes literuature, newsletters and articles available from The Pituitary Foundation as well as the contact information for other organisations who provide support and information. All of our patient leaflets are available to read as well as downloadable in PDF format from this website. Resources for GPsEndotext.org ‘Your Endocrine Source’ www.endotext.org (www.endotext.org/neuroendo/index.htm) Oxford Handbook of Endocrinology OUP (2002) JAH Wass & H Turner (Eds). More Specialist ResourcesManagement of Pituitary Tumors: The Clinician’s Practical Guide (2003) (Second Edition), Editors and authors Michael P. Powell, Stafford L. Lightman and Edward R. Laws. Humana Press, Totowa, New Jersey Pituitary Tumours. Recommendations for service provision and guidelines for management of patients. Consensus statement of a working party (1997) RN Clayton & JAH Wass (Eds) London: Royal College of Physicians The Diagnosis and Treatment of Pituitary Insufficiency (1997) Lamberts SWJ (Ed) Bristol, UK: BioScientifica Endocrinology (1997) Levy A & Lightman SL New York: Oxford University Press The Epidemiology, Pathogenesis and Management of Pituitary Tumours (1998) Webb SM (Ed) Bristol, UK: BioScientifica
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