Anterior & Posterior Pituitary Gland PDF

Summary

This document is a detailed overview of the anterior and posterior pituitary glands. It covers various conditions, including pituitary adenomas, hypopituitarism, and different types of diabetes insipidus. The content focuses on the functioning, diseases, diagnoses, and treatments related to the pituitary glands.

Full Transcript

# Anterior Pituitary Gland ## I. Pituitary Adenoma - Benign tumor of anterior pituitary cells - May be functional (hormone-producing) or nonfunctional (silent) - **Nonfunctional tumors** often present with mass effect - Bitemporal hemianopsia occurs due to compression of the optic chi...

# Anterior Pituitary Gland ## I. Pituitary Adenoma - Benign tumor of anterior pituitary cells - May be functional (hormone-producing) or nonfunctional (silent) - **Nonfunctional tumors** often present with mass effect - Bitemporal hemianopsia occurs due to compression of the optic chiasm - Hypopituitarism occurs due to compression of normal pituitary tissue - Headache - **Functional tumors** present with features based on the type of hormone produced. ## C. Prolactinoma - Presents as galactorrhea and amenorrhea (females) or as decreased libido and headache (males); most common type of pituitary adenoma - Treatment is dopamine agonists (e.g., bromocriptine or cabergoline) to suppress prolactin production (shrinks tumor) or surgery for larger lesions. ## D. Growth hormone cell adenoma - Gigantism in children - increased linear bone growth (epiphyses are not fused) - Acromegaly in adults - Enlarged bones of hands, feet, and jaw - Growth of visceral organs leading to dysfunction (e.g., cardiac failure) - Enlarged tongue - Secondary diabetes mellitus is often present (GH induces liver gluconeogenesis). - Diagnosed by elevated GH and insulin growth factor-1 (IGF-1) levels along with lack of GH suppression by oral glucose - Treatment is octreotide (somatostatin analog that suppresses GH release), GH receptor antagonists, or surgery. ## E. ACTH cell adenomas - Secrete ACTH leading to Cushing syndrome (see "Adrenal Cortex" below). ## F. TSH cell, LH-producing, and FSH-producing adenomas - Occur, but are rare. # II. Hypopituitarism - Insufficient production of hormones by the anterior pituitary gland - Symptoms arise when >75% of the pituitary parenchyma is lost. ## B. Causes include - Pituitary adenomas (adults) or craniopharyngioma (children) - due to mass effect or pituitary apoplexy (bleeding into an adenoma) - Sheehan syndrome - pregnancy-related infarction the of pituitary gland - Gland doubles in size during pregnancy, but blood supply does not increase significantly; blood loss during parturition precipitates infarction. - Presents as poor lactation, loss of pubic hair, and fatigue - Empty sella syndrome - congenital defect of the sella - Herniation of the arachnoid and CSF into the sella compresses and destroys the pituitary gland. - Pituitary gland is "absent" (empty sella) on imaging. # Posterior Pituitary Gland ## I. Basic Principles - Antidiuretic hormone (ADH) and oxytocin are made in the hypothalamus and then transported via axons to the posterior pituitary for release. - ADH acts on the distal tubules and collecting ducts of the kidney to promote free water retention. - Oxytocin mediates uterine contraction during labor and release of breast milk (let-down) in lactating mothers. ## II. Central Diabetes Insipidus - ADH deficiency - Due to hypothalamic or posterior pituitary pathology (e.g., tumor, trauma, infection, or inflammation) - Clinical features are based on loss of free water. - Polyuria and polydipsia with risk of life-threatening dehydration - Hypernatremia and high serum osmolality - Low urine osmolality and specific gravity - Water deprivation test fails to increase urine osmolality (useful for diagnosis). - Treatment is desmopressin (ADH analog). ## III. Nephrogenic Diabetes Insipidus - Impaired renal response to ADH - Due to inherited mutations or drugs (e.g., lithium and demeclocycline) - Clinical features are similar to central diabetes insipidus, but there is no response to desmopressin. ## IV. Syndrome of Inappropriate ADH (SIADH) Secretion - Excessive ADH secretion - Most often due to ectopic production (e.g., small cell carcinoma of the lung); other causes include CNS trauma, pulmonary infection, and drugs (e.g., cyclophosphamide). - Clinical features are based on retention of free water - Hyponatremia and low serum osmolality - Mental status changes and seizures - Hyponatremia leads to neuronal swelling and cerebral edema. - Treatment is free water restriction or demeclocycline.

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