Pituitary disorders result from the dysfunction of the pituitary gland or its tumours that impair the balance of vital hormones and need specific interventions. This pea-sized gland’s central role in endocrine function means treatment strategies must address hormonal imbalances and structural abnormalities.
However, early detection and timely treatment of pituitary disorders can prevent serious hormone imbalances.
Read below to understand how pituitary disorders are treated and how thyroid function may be affected.
Treatment genuinely relies on the specific type of disorder, the hormones at play, and the characteristics of the tumour. A combined approach is often essential, bringing together surgery, medication, and radiation to tackle the underlying issue effectively.
1. Surgical Intervention
Endocrinologists suggest transsphenoidal surgery for most pituitary tumours (excluding prolactinomas) as the first-line treatment.
The benefits of this process include:
Risks, however, include hypopituitarism (3–20%), diabetes insipidus (5–30%), and CSF leaks (1–5%), depending on tumor characteristics and surgical technique.. Endoscopic technologies have already achieved the same effectiveness as the traditional ones but with fewer complications.
2. Medication Therapy
Medications are available to address hormone overproduction, minimise the effects of deficiencies, or even shrink tumours. Here's how various medications can curb the impact of different pituitary disorders:
Pituitary Condition | Key Medications | Purpose |
Prolactinomas | Cabergoline, Bromocriptine | Dopamine agonists shrink tumors in 80–90% of cases and thus are often preferred over surgery. |
Acromegaly | Somatostatin analogs (Octreotide, Pasireotide), Pegvisomant | These medications reduce GH secretion or block its effects. However, Pasireotide may cause hyperglycemia. |
Cushing’s | Ketoconazole, Mifepristone | Their dosages inhibit cortisol production or block its receptors. Mifepristone intake, however, requires glucose monitoring. |
OHSU is highlighting some promising new therapies, including pasireotide for Cushing's disease and acromegaly, as well as mifepristone to control hyperglycaemia in Cushing's. These medications have been rigorously tested through clinical trials. These drugs may be used as alternatives or post-surgery.
3. Radiation Therapy
When it comes to treating residual or recurrent tumours, radiation therapy can effectively manage hormonal control in about 70–83% of cases over months to years.
Stereotactic radiosurgery may achieve hormonal control faster (e.g., 12–24 months) than conventional radiation (18–60 months), but response depends on tumor type and hormone profile. However, it is essential to remember that this approach has an 18% risk of recurrence.
4. Hormone Replacement
To prevent the effects of pituitary hypothyroidism, doctors usually recommend:
Dosing requires careful titration to avoid under- or overtreatment.
In pituitary (secondary) hypothyroidism, the pituitary gland is unable to stimulate enough TSH, and, as a result, the thyroid gland does not produce enough thyroid hormones. When we talk about primary hypothyroidism, which is a thyroid issue, this condition occurs in ~5% of cases and often coexists with other pituitary deficiencies.
Causes and Symptoms of Pituitary Thyroid Deficiency
Diagnosis and Management of Pituitary Thyroid Deficiency
With treatment, the prognosis for secondary hypothyroidism is typically excellent, with most patients seeing their thyroid hormone levels normalise and a substantial reduction in symptoms. In addition, minimally invasive surgery and targeted medications have led to better outcomes, although ongoing monitoring is crucial.
Close coordination with healthcare providers is essential for maintaining optimal hormonal balance and improving the quality of life in individuals managing complex pituitary disorders.
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