Pituitary adenoma

Last updated: April 22, 2021

Pituitary adenoma

Watch later

Watch later

Complement deficiency
Complement system
Glycogen metabolism
Gluconeogenesis
Fatty acid synthesis
Fatty acid oxidation
Antibody classes
Cell-mediated immunity of CD4 cells
Cell-mediated immunity of natural killer and CD8 cells
B-cell activation, differentiation, and contraction
T-cell activation
B-cell development
Monoclonal antibodies
Vitamin B12 deficiency
Folate (Vitamin B9) deficiency
Iron deficiency anemia
Sideroblastic anemia
Microcytic anemia: Pathology review
Macrocytic anemia: Pathology review
Autoimmune hemolytic anemia
Sickle cell disease (NORD)
Anemia of chronic disease
Alpha-thalassemia
Beta-thalassemia
Platelet plug formation (primary hemostasis)
Clot retraction and fibrinolysis
Disseminated intravascular coagulation
Von Willebrand disease
Heparin-induced thrombocytopenia
Thrombotic thrombocytopenic purpura
Hemolytic-uremic syndrome
Immune thrombocytopenia
Coagulation disorders: Pathology review
Mixed platelet and coagulation disorders: Pathology review
Platelet disorders: Pathology review
Thrombosis syndromes (hypercoagulability): Pathology review
Hemophilia
Adrenal gland histology
Pheochromocytoma
Pituitary gland histology
Cushing syndrome
Hyperprolactinemia
Prolactinoma
Pituitary adenoma
Sheehan syndrome
Growth hormone deficiency
Primary adrenal insufficiency
Hyperaldosteronism
Cortisol
Synthesis of adrenocortical hormones
Diabetes mellitus
Diabetes insipidus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Glucagon
Insulin
Adrenal insufficiency: Pathology review
Adrenal masses: Pathology review
Cushing syndrome and Cushing disease: Pathology review
Diabetes insipidus and SIADH: Pathology review
Diabetes mellitus: Pathology review
Hyperthyroidism: Pathology review
Hypopituitarism: Pathology review
Hypothyroidism: Pathology review
Multiple endocrine neoplasia: Pathology review
Neuroendocrine tumors of the gastrointestinal system: Pathology review
Parathyroid disorders and calcium imbalance: Pathology review
Pituitary tumors: Pathology review
Thyroid nodules and thyroid cancer: Pathology review
Ascending and descending spinal tracts
Blood brain barrier
Cerebral circulation
Cerebrospinal fluid
Cranial nerves
Nervous system anatomy and physiology
Neuron action potential
Adrenergic receptors
Sympathetic nervous system
Cholinergic receptors
Parasympathetic nervous system
Enteric nervous system
Motor cortex
Muscle spindles and golgi tendon organs
Pyramidal and extrapyramidal tracts
Sensory receptor function
Somatosensory pathways
Somatosensory receptors
Anatomy of the male reproductive organs of the pelvis
Nerves and lymphatics of the pelvis
Estrogen and progesterone
GERD, peptic ulcers, gastritis, and stomach cancer: Pathology review

Transcript

Watch video only

Pituitary adenoma can be broken down - “adeno” refers to a gland and “oma” refers to a tumor, so pituitary adenoma is a tumor that develops in the hormone-producing cells of the pituitary gland.

Normally, the pituitary is a pea-sized gland, hanging by a stalk from the base of the brain.

It sits just behind the eyes near the optic chiasm, which is where the optic nerves cross.

The anterior pituitary, which is the front of the pituitary gland, contains a few different types of cells, each of which secretes a different hormone.

The largest group of cells are the somatotropes which secrete growth hormone, or GH for short, which goes on to promote tissue and organ growth.

The second largest cell group are the corticotrophs which secrete adrenocorticotropic hormone, or ACTH for short.

ACTH stimulates the adrenal glands to secrete cortisol, a hormone that controls the stress response and metabolic regulation.

A smaller cell group are the lactotrophs which secrete prolactin.

Prolactin stimulates breast milk production, and also inhibits ovulation, which is when an egg cell is released from the ovary, and inhibits spermatogenesis, which is the development of sperm cells.

There are also thyrotrophs which are cells that secrete thyroid stimulating hormone, or TSH which goes on to stimulate the thyroid gland.

And finally, there are also gonadotrophs which secrete two gonadotropic hormones - luteinizing hormone, or LH, and follicle-stimulating hormone, or FSH, both of which go on to stimulate the ovaries or testes.

In pituitary adenomas, one of these cells mutates and becomes neoplastic, meaning that it starts dividing uncontrollably and over time it forms a tumor.

But these cells don’t invade neighboring tissues, so this is considered a benign tumor rather than a malignant one.

Pituitary adenomas can be classified by their size, adenomas smaller than 1cm are called microadenomas, and those larger than 1cm are called macroadenomas.

Macroadenomas are more likely to compress surrounding structures like the meninges, which is the protective layer overlying the brain that typically causes pain when it’s stretched.

Macroadenomas can also compress optic nerves as they cross at the optic chiasm.

That can affect a person’s ability to view things that are in the temporal visual field of both eyes, also called “bitemporal hemianopia”.

Finally, the compression can also affect other healthy pituitary cells and interfere with their ability to make hormones.

Pituitary adenomas that secrete hormones are called functional adenomas, whereas those that don’t are called non-functional adenomas.

Functional pituitary adenomas are divided into a few different types depending on the cells that they arise from and the hormone these cells produce.

The most common type of pituitary adenoma is a prolactinoma which arises from lactotrophs that make prolactin.

In women, excess prolactin causes amenorrhea, which is when there is loss of menstrual bleeding and galactorrhea, which is a milky nipple discharge.

In men, excess prolactin causes a low libido - a low sex drive and gynecomastia or breast enlargement.

The second most common type of pituitary adenoma arises from somatotropes that make growth hormone.

Key Takeaways

Pituitary adenomas are benign tumors that occur in the pituitary gland. They vary depending on their size and the type of hormones they produce. Some pituitary adenomas do not produce any hormones and are referred to as non-functioning adenomas, while others produce hormones that can cause a wide range of symptoms.

Common symptoms include headaches, visual disturbances, fatigue, and changes in sexual function or menstrual cycles. The most common types involve lactotrophs that make prolactin, somatotrophs that make growth hormones, and corticotrophs that make ACTH. They are usually diagnosed by checking hormone levels and obtaining an MRI and are treated with medications or surgery.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
  4. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  5. "Harrison's Endocrinology, 4E" McGraw-Hill Education / Medical (2016)
  6. "Management of hormone-secreting pituitary adenomas" Neuro-Oncology (2016)
  7. "The prevalence of pituitary adenomas" Cancer (2004)