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Flashcards covering key vocabulary and concepts related to hypothalamus and pituitary gland diseases.
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Hypothalamus
A brain structure located on top of the brainstem, part of the diencephalon, involved in maintaining homeostasis and regulating endocrine and autonomic functions.
Pituitary Gland
A pea-sized gland located in the sella turcica of the sphenoid bone, responsible for hormone production and regulation of various bodily functions.
Anterior Pituitary
Front lobe of the pituitary gland that secretes hormones like ACTH, FSH, LH, and GH, influenced by hypothalamic releasing hormones.
Posterior Pituitary
Back lobe of the pituitary gland that stores and releases hormones like ADH and oxytocin, produced in the hypothalamus.
ADH (Vasopressin)
A hormone released from the posterior pituitary that regulates water retention in the kidneys and helps control blood pressure.
Oxytocin
A hormone released from the posterior pituitary involved in childbirth, lactation, and emotional bonding.
Hypopituitarism
A condition characterized by decreased secretion of one or more of the hormones produced by the pituitary gland.
Acromegaly
A disorder caused by excess growth hormone, characterized by enlarged features and often associated with pituitary adenomas.
Cushing's Disease
A condition caused by an ACTH-secreting pituitary tumor, leading to excessive cortisol levels and symptoms of obesity, hypertension, and glucose intolerance.
Circadian Rhythms
Biological processes that follow a roughly 24-hour cycle, regulated by the suprachiasmatic nucleus in the hypothalamus.
Diabetes Insipidus
A condition resulting from decreased ADH release, leading to polyuria and excessive thirst.
SIADH (Syndrome of Inappropriate ADH Secretion)
A condition characterized by excessive secretion of ADH despite normal or increased plasma volumes, leading to hyponatremia.
Prader-Willi Syndrome
A genetic disorder resulting in obesity, cognitive impairment, and endocrine issues, caused by the absence of expression of specific genes on chromosome 15.
Kallmann Syndrome
A condition characterized by delayed or absent puberty and an impaired sense of smell due to lack of GnRH.
Hypothalamic Dysfunction
Dysfunction in the hypothalamus that can affect hunger, thirst, body temperature control, and hormonal regulation.
Pituitary Tumors
Abnormal growths in the pituitary gland, which can cause hormonal dysfunction and various neurological symptoms.
Empty Sella Syndrome
A condition where the sella turcica appears empty because it's filled with cerebrospinal fluid, affecting pituitary function.
Visual Field Defects
Loss of vision in certain areas, commonly seen in patients with pituitary adenomas affecting the optic chiasm.
Treatment of SIADH
Difficult to differentiate from cerebral salt wasting; typically requires hypertonic saline.
Neurogenic Fever
A fever resulting from damage to the hypothalamus, often associated with brain hemorrhages.
Hypothalamus Location
On top of the brainstem, at the center of the brain, inferior to the thalamus.
Hypothalamus Borders (Rostral)
Optic chiasm, lamina terminalis, anterior commissure.
Hypothalamus Borders (Posterior)
Mammillary bodies.
Hypothalamus Borders (Inferior)
Tuber cinereum tapering into median eminence leading to infundibular stalk.
Hypothalamus Borders (Lateral)
Internal capsule.
Hypothalamus Midline Structure
The 3^{rd} ventricle.
Hypothalamus Primary Function
Maintains homeostasis by controlling endocrine and autonomic functions, linking nervous and endocrine systems.
Hypothalamus Regulation Examples
Body temperature, weight/appetite, childbirth/lactation, growth, sleep-wake cycle, sexual drive, emotion regulation.
Normal Body Temperature
Approximately 37^ ext{o} ext{C} (98.6^ ext{o} ext{F}).
Body Response to Heat
Vasodilation of skin blood vessels, sweating.
Body Response to Cold
Vasoconstriction of skin blood vessels, shivering, piloerection.
Anterior Hypothalamic Region Function
Autonomic (parasympathetic) and neuroendocrine control.
Tuberal Hypothalamic Region Function
Feeding/satiety.
Posterior Hypothalamic Region Function
Sympathetic tone and memory/learning.
Anterior/Medial Nuclei Control
Parasympathetic responses (decrease heart rate, increase saliva secretion, pupillary constriction).
Posterior/Lateral Hypothalamus Control
Sympathetic responses (increased heart rate, increased blood pressure, pupillary dilation).
Preoptic Nucleus Hormone
Gonadotropin-releasing hormone (GnRH).
Paraventricular Nucleus Hormones
Oxytocin, vasopressin (ADH), Corticotropin-releasing hormone (CRH), Thyrotropin-releasing hormone (TRH).
Supraoptic Nucleus Hormones
Vasopressin (ADH), oxytocin.
Suprachiasmatic Nucleus Function
Circadian rhythms.
Anterior Hypothalamic Nucleus Function
Body temperature.
Arcuate Nucleus Hormones
Growth hormone-releasing hormone (GHRH), prolactin-inhibiting hormone (dopamine).
Ventromedial Nucleus Function
Satiety center.
Dorsomedial Nucleus Function
Emotional response, blood pressure control.
Mammillary Nucleus Function
Emotion, memory.
Posterior Hypothalamic Nucleus Function
Blood pressure regulation, thermoregulation.
Magnocellular Regions
Supraoptic and paraventricular nuclei that produce oxytocin and vasopressin.
Posterior Pituitary Hormone Transport
Oxytocin and vasopressin are transported via axonal systems from magnocellular neurons to the posterior pituitary.
Anterior Pituitary Hormone Signal Transport
Hormonal signals from the hypothalamus are transported via the tuberoinfundibular tract to the anterior pituitary.
Causes of Hypothalamic Dysfunction
Brain surgery, traumatic brain injury, brain tumors, radiation, genetic disease, nutritional deficiency, infection and inflammation.
Pituitary Gland Anatomy
Pea-sized gland in middle cranial fossa within the sella turcica of the sphenoid bone. Consists of anterior and posterior lobes.
Pituitary Gland Superior Border
Optic chiasm.
Pituitary Gland Lateral Border
Cavernous sinus.
Neurohypophysis (Posterior Pituitary)
Formed from neural tissue (infundibulum) and stores/releases ADH and oxytocin.
Adenohypophysis (Anterior Pituitary)
Formed from glandular tissue (Rathke's pouch) and synthesizes/secretes its own hormones.
Anterior Pituitary Hormones
ACTH, Prolactin, GH, TSH, FSH, LH.
Posterior Pituitary Hormones
Oxytocin, Vasopressin (ADH).
Anterior Pituitary Hormonal Control
Regulated by releasing and inhibiting hormones from the hypothalamus, released into the portal circulation.
Posterior Pituitary Hormonal Release
Hormones secreted from axon endings directly enter the bloodstream.
Mass Lesions of Pituitary
Adenomas, cysts, or metastatic cancers affecting pituitary function.
Microadenomas Size
Macroadenomas Size
≥1 cm.
Neurologic Symptom of Pituitary Tumor
Visual impairment (bitemporal hemianopsia) due to optic chiasm compression, headaches.
Bitemporal Hemianopsia
Loss of vision in the outer half of both visual fields.
Pituitary Apoplexy
Medical emergency, sudden hemorrhage in a macroadenoma, severe headache, neck stiffness, visual changes.
Presentations of Pituitary Tumors (Deficiencies)
Central diabetes insipidus, hormonal deficiencies (e.g., GH, gonadotropins).
Presentations of Pituitary Tumors (Excess)
Cushing's Disease (ACTH excess), Gigantism/Acromegaly (GH excess), Galactorrhea (Prolactin excess).
Acromegaly Cause
Excessive secretion of growth hormone (GH) in adulthood.
Growth Hormone Deficiency Symptoms in Children
Stunted growth, short stature, delayed puberty, increased body fat.
Prolactinoma Manifestations
Galactorrhea, amenorrhea, infertility, decreased libido.
Hyperprolactinemia
Elevated prolactin levels, often due to prolactinomas, inhibiting GnRH secretion.
Primary Evaluation of Pituitary Function
Serum hormone analysis and imaging (MRI) for structural abnormalities.
SIADH
Syndrome of Inappropriate Antidiuretic Hormone.
Diabetes Insipidus (DI)
Disorder of water balance due to insufficient ADH (central DI) or kidney insensitivity to ADH (nephrogenic DI).
Wolfram Syndrome
Rare genetic disorder affecting multiple systems, including diabetes mellitus, diabetes insipidus, optic atrophy, and deafness (DIDMOAD).
Prader-Willi Syndrome
Genetic disorder characterized by chronic hunger, intellectual disability, hypotonia, and hypogonadism, related to hypothalamic dysfunction.
Kallman Syndrome
Genetic disorder causing hypogonadotropic hypogonadism combined with anosmia (loss of smell), due to failure of GnRH neurons to migrate.
Treatments for Hypothalamic/Pituitary Dysfunction
Hormonal replacements, surgical interventions, supportive care for symptom management.
Christina Lenk, MD Email
65201@yahoo.com