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The Adrenals. דר. אביטל נחמיאס. The Adrenals. Structure and function Cortex Hypofunction – Addison Hyperfunction – Cushing Adrenal incidentaloma. The Adrenal Glands. בלוטת יותרת הכליה היא איבר רטרופריטוניאלי שנראה כמו כובע משולש מעל כל כליה
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The Adrenals דר. אביטל נחמיאס
The Adrenals • Structure and function • Cortex • Hypofunction – Addison • Hyperfunction – Cushing • Adrenal incidentaloma
The Adrenal Glands בלוטת יותרת הכליה היא איבר רטרופריטוניאלי שנראה כמו כובע משולש מעל כל כליה המשקל של כל בלוטה הוא כ-4 גרם והמידות הן 2-3 X 4-6 cm
The Adrenal Glands Retroperitoneal 4 gr weight 2X4X1 cm
Morphology of the Adrenal Cortisol DHEA Aldosterone Cathecholeamines Medulla Reticularis Fasciculata Glomerulosa
Adrenal Cortex Zona glomerulosa- 15% Mineralocorticoid - Aldosterone Zona fasciculata- 75% Glucocorticoid - Cortisol and DHEA Zona reticularis- 10% Androgens - DHEA (DeHydroEpiAndrosterone), DHEAS DHEAS הוא ההורמון הפעיל שאחראי על כל סימני הויריליזציה
Actions of glucocorticoids • Immune system • ↑ WBC, ↓Eos, ↓ phagocytosis, anti inflammatory • Metabolic • Increase gluconeogenesis • Inhibit glucose uptake and utilization (NOT in brain, heart, liver, RBC) • Increase lipolysis, increase protein catabolism - myopathy • Impaired wound healing (less colagen production, impaired fibroblast function) • Inhibit osteoblasts (osteoporosis), ↓ intestinal and renal calcium absorption – increases PTH • Developmental • Differentiation of organs in the fetus • Complex action on the brain - arousal and cognition
Action of mineralocorticoids • Increased Na absorption in the kidney – water comes with the Na – fluid overload – hypertention and edema • K+ secreted instead of the Na – hypokalemia
Regulation of aldosterone secretion • RAS • K+ • ACTH
Regulation of androgen secretion • Adrenal androgen secretion is regulated by ACTH • In males – adrenal androgens have minimal effects • In females – adrenal androgens convert to testosterone in extraglandular tissues
Laboratory evaluation of adrenal function What’s the problem?
Laboratory evaluation of adrenal function • Point measurements – at peak or trough • Urinary excretion • Dynamic testing • Stimulation – for suspected deficiency • Suppression – for suspected excess
Stimulation tests • Cortisol • ACTH (synacthen test) • Aldosterone • Volume depletion • Salt restriction • Diuretic administration • Upright posture
Suppression test • Cortisol • Dexamethasone suppression test • Aldosterone • Saline infusion test
Adrenal Failure • Primary (Addison’s Disease) Adrenal dysfunction Both GC and MC deficiency; ACTH. • Secondary Pituitary Dysfunction Only GC deficiency;ACTH.
“general languor and debility, feebleness of the heart's action, irritability of the stomach, and a peculiar change ofthe color of the skin" Thomas Addison The first description of Addison’s disease
Etiology of Addison’s Disease Autoimmune (80%) Isolated, Autoimmune polyglandular syndrome Type 1&2 Infections TB (calcifications), Histoplasmosis, CMV, HIV, syphillis, coccidioidomycosis, and cryptococcosis. Infiltration Amyloidosis, Hemochromatosis Hemorrhage Anticoagulants, trauma, sepsis, surgery, pregnancy, Meningococcemia causes waterhouse friderichsen syndrome – adrenal crisis) Infarction (bilateral – rare)
Etiology of Addison’s Disease • Bilateral Metastasis, Lymphoma (rare) • Bilateral adrenalectomy • Drugs • Inhibitors of steroidogenesis (ketoconazol) • Increase metabolism of steroid hormones (tegretol) • Congenital Adrenal Hyperplasia • Familial GC deficiency
Secondary Hypoadrenalism (ACTH) • Iatrogenic • Abrupt withdrawal of Chronic steroid Rx • Pituitary • Tumor (stalk effect) • Radiation • Surgery • Infarct • Hemorrhage • Sheehan syn – low BP during birth +/- hemorrhage
Autoimmune Addison’s Disease • Autoimmune Polyglandular Syndrome Type 1 • AR inheritance • More common in Iranian Jews • Hypoparathyroidism • Chronic Mucocutaneous Candidiasis • Gonadal failure • Addison • Ab in serum can be sent abroad
Autoimmune Addison’s Disease • Autoimmune Polyglandular Syndrome Type 2 • 50:1,000,000 rare • More common in women, age 30-50 • DM type 1 • Vitiligo • Graves or hashimoto • Addison • Pernicious anemia
Clinical Features of Adrenal Insufficiency Chronic syndrome Symptoms (not specific): Weakness & fatigue 100% Anorexia 100% Gastrointestinal symptoms 92% Signs: Weight loss 100%Hyperpigmentation (primary) 92% Hypotension 88% Salt craving (primary) 19% Postural hypotension symptoms 12% Asthenia
Hyperpigmentation ל ACTH ברמות גבוהות יש פעילות של MSH הורמון המפעיל מלנוציטים
Laboratory Findings • Normocytic normochromic anemia (chronic disease) • Neutropenia and eosinophilia, relative lymphocytosis • Hyponatremia (SIADH, MC def) (90%) • Hyperkalemia (65%) • Hypoglycemia (rare) • Hypercalcemia (rare)
Diagnosis • Primary adrenal insufficiency: • Rapid ACTH test (Synacthen 250 mg) • Post-stimulation cortisol (30’ 60’) above 550 nmol/l (20 mg/dl) is normal, Below 200 could be addison • Plasma ACTH levels • Secondary/ tertiary adrenal insufficiency: • CRH test
Acute Syndrome (Addisonian Crisis) • Withdrawal • Acute stress • Infection • trauma • Surgery • Dehydration • Acute syndrome • Hemorrhage • Infarct • Meningococcemia (Waterhouse-Friderichsen syndrome) • Rare in secondary adrenal insufficiency.
Acute Syndrome (Addisonian Crisis) • Manifestations: • Shock and hypotension • Weakness, fatigue, lethargy • Muscle, joint and abdominal pain (acute abdomen) • Fever, anorexia, vomiting • Apathy, Clouded sensorium • Hypoglycemia is rare • The diagnosis should always be considered in any patient with unexplained shock
Treatment This is a life threatening emergency!!! • Acute Crisis • Hydrocortisone 100 mg IV, every 6-8 hours for 24 hr not PO !!! • Correct volume depletion, dehydration, hypotension • and hypoglycemia with IV saline and glucose • Correct precipitating factors, especially infection • As soon as the patient is eating and drinking and off IV fluids add fludrocortisone.
Maintenance • Hydrocortisone 15-20 mg in the morning & 5-10 mg at 4-6 PM or prednisone 5-7.5 mg orally once a day • Fludrocortisone 0.05-2 mg/day (primary) • Follow clinical symptoms, weight, B.P., electrolytes • Educate patient to increase cortisol dose during stress
Cushing’s disease Harvey Williams Cushing
Etiology of Cushing’s syndrome (CS) Exogenous: (Iatrogenic, Factitious) Endogenous: ACTH dependent: Pituitary (68%) Ectopic ACTH (SCLC)(15%) CRH rare ACTH independent: Adenoma (9%) Carcinoma (8%) Nodular hyperplasia rare Cushing’s disease
Ectopic ACTH secretion *hypokalemia
Cushing’s Syndrome- Symptoms Feature % Weight gain 91 Hirsutism, acne 82 Menstrual disturbances/Dec. libido 76 Psychiatric dysfunction 60 Back pain 43 Muscular weakness 29 Fractures (osteoporosis) Infections
Cushing’s Syndrome- Signs Feature % Central obesity (viceral fat) 97 Plethora 94 Moon face 88 HTN 74 Easy bruising (colagen fibroblasts) 62 Red striae 56 Muscle weakness 56 Edema 50