Pituitary Adenoma

Pituitary adenomas are benign neoplasms arising from the hormone-secreting cells of the anterior pituitary gland. They are classified by size (microadenoma under 1 cm, macroadenoma 1 cm or larger) and by hormonal activity (functional vs non-functional), with prolactinomas being the most common subtype.

Understanding Pituitary Adenomas

Pituitary adenomas account for 10–15 per cent of all intracranial neoplasms. The pituitary gland sits within the sella turcica at the base of the skull, surrounded by critical structures: the optic chiasm superiorly, the cavernous sinuses laterally (containing the internal carotid arteries and cranial nerves III, IV, V, and VI), and the sphenoid sinus inferiorly. As a pituitary adenoma enlarges, it may compress the optic chiasm, producing visual field deficits, or invade the cavernous sinus, limiting surgical resectability. Hormonally active adenomas cause distinct clinical syndromes depending on the hormone secreted: prolactin, growth hormone (acromegaly), ACTH (Cushing's disease), TSH, or gonadotropins.

Transsphenoidal surgery is the first-line treatment for most pituitary adenomas except prolactinomas, which are primarily managed medically. Istanbul provides access to elite pituitary surgeons who perform high-volume transsphenoidal resections with outcomes comparable to leading international centres.

Pituitary Adenoma

Treatment Options for Pituitary Adenoma

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Symptoms of Pituitary Adenoma

Clinical presentation follows three patterns: mass effect, hormonal excess, and hormonal deficiency. Mass effect symptoms include headache, visual field deficits (classically bitemporal superior quadrantanopia progressing to bitemporal hemianopia from chiasmal compression), and hypopituitarism from compression of normal pituitary tissue. Pituitary apoplexy — haemorrhage or infarction of the adenoma — presents with sudden severe headache, visual loss, ophthalmoplegia, and haemodynamic collapse requiring emergency surgical decompression. Hormonal excess syndromes include hyperprolactinaemia (galactorrhoea, amenorrhoea, infertility), acromegaly, and Cushing's disease.

Diagnostic Pathways

Pituitary MRI with thin-section gadolinium-enhanced sequences is the essential imaging study, defining the adenoma's size, signal characteristics, cavernous sinus invasion (Knosp grade), and relationship to the optic chiasm. Formal visual field testing (Humphrey perimetry) documents any chiasmal or optic nerve compression. Hormonal evaluation includes prolactin, IGF-1, ACTH, cortisol, TSH, free T4, FSH, LH, and in males, testosterone. Transsphenoidal biopsy may be needed for non-functioning adenomas where tissue diagnosis is required to guide management.

Advanced Treatment Options at Vellum Select

Transsphenoidal Adenomectomy

Pituitary Tumour Treatment in Turkey via transsphenoidal approach is the first-line treatment for most non-prolactinoma pituitary adenomas. Prof. Dr. Türker Kılıç performs both microscopic and fully endoscopic transsphenoidal resection using intraoperative image guidance to maximise resection while preserving normal pituitary function. Remission rates for functional microadenomas exceed 85 per cent. Hospital stay is typically 24–48 hours with no external incision.

Craniotomy

For large adenomas with significant suprasellar extension not amenable to transsphenoidal surgery, Craniotomy (Brain Surgery) in Turkey may be necessary.

Gamma Knife Radiosurgery

For residual or recurrent adenomas not amenable to surgical re-resection, Gamma Knife Radiosurgery in Turkey offers effective tumour control and can normalise hormone hypersecretion in functioning adenomas.

To discuss your pituitary adenoma diagnosis with Prof. Dr. Türker Kılıç, view his profile or contact Vellum Select to arrange a consultation.

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