Adrenal Disorders for the USMLE, Step One: Abnormalities of the Fasciculata: Hypocortisolism

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Adrenal Disorders for the USMLE, Step One: Abnormalities of the Fasciculata: Hypocortisolism Howard Sachs, MD Patients Course, 2017 Associate Professor of Clinical Medicine UMass Medical School

Manifestations Aldosterone Cortisol Response Anything else Etiologies Normal Physiology

Etiololgy of Hypocortisolism Acute, Shock Pituitary Apoplexy Adrenal Hemorrhage HPA Failure Acute cessation+ Chronic: HPA axis failure Hypothalamus Infiltrative disorders Pituitary Sheehan s Adenoma/Mass effect Adrenal Autoimmune Infiltrative (bait-switch) Tumor Infection CAH (enzyme deficiency) HPA Failure Cessation: exogenous CCS

Etiololgy of Hypocortisolism Acute, Shock Pituitary Apoplexy Adrenal Hemorrhage HPA Failure Acute cessation+ Chronic: HPA axis failure Hypothalamus Infiltrative disorders Pituitary Sheehan s Adenoma/Mass effect Adrenal Autoimmune Infiltrative (bait-switch) Tumor Infection CAH (enzyme deficiency) HPA Failure Cessation: exogenous CCS

Etiololgy of Hypocortisolism Acute, Shock Pituitary Apoplexy Adrenal Hemorrhage HPA Failure Acute cessation+ Chronic: HPA axis failure Hypothalamus Infiltrative disorders Pituitary Sheehan s Adenoma/Mass effect Adrenal Autoimmune Infiltrative (bait-switch) Tumor Infection CAH (enzyme deficiency) HPA Failure Cessation: exogenous CCS

Etiololgy of Hypocortisolism Acute, Shock Pituitary Apoplexy Adrenal Hemorrhage HPA Failure Acute cessation+ Chronic: HPA axis failure Hypothalamus Infiltrative disorders Pituitary Sheehan s Adenoma/Mass effect Adrenal Autoimmune Infiltrative (bait-switch) Tumor Infection CAH (enzyme deficiency) HPA Failure Cessation: exogenous CCS

Etiololgy of Hypocortisolism Acute, Shock Pituitary Apoplexy Adrenal Hemorrhage HPA Failure Acute cessation+ Chronic: HPA axis failure Hypothalamus Infiltrative disorders Pituitary Sheehan s Adenoma/Mass effect Adrenal Autoimmune Infiltrative (bait-switch) Tumor Infection CAH (enzyme deficiency) HPA Failure Cessation: exogenous CCS

Etiololgy of Hypocortisolism Acute, Shock Pituitary Apoplexy Adrenal Hemorrhage HPA Failure Acute cessation+ Chronic: HPA axis failure Hypothalamus Infiltrative disorders Pituitary Sheehan s Adenoma/Mass effect Adrenal Autoimmune Infiltrative (bait-switch) Tumor Infection CAH (enzyme deficiency) HPA Failure Cessation: exogenous CCS

Adrenalitis (Addison s Disease) Infiltrative Disorders G Adrenal Hemorrhage F Sepsis R Primary Adrenal Failure: High CRH and ACTH PHEO

Manifestions of Insidious Hypocortisolism (Hypoadrenalism) Cardiovascular GI Hypotension ( -1 tone) Nausea, anorexia Endo Weight loss,fatigue, weakness, hypoglycemia Heme Eosinophilia Derm (if 1 adrenal failure) Hyperpigmentation

Manifestions of Insidious Hypocortisolism (Hypoadrenalism) Cardiovascular GI Hypotension ( -1 tone) Nausea, anorexia Endo Weight loss,fatigue, weakness, hypoglycemia Heme Eosinophilia Derm (if 1 adrenal failure) Hyperpigmentation CRH Proopiomelanocortin (POMC) ACTH and MSH

Manifestions of Insidious Hypocortisolism (Hypoadrenalism) Cardiovascular GI Hypotension ( -1 tone) Nausea, anorexia Endo Weight loss,fatigue, weakness, hypoglycemia Heme Eosinophilia Derm (if 1 adrenal failure) Hyperpigmentation Renal (if adrenal failure hypoaldosteronism) Type IV, RTA Failure of aldosterone stimulation of H+-ATPase pump Both contribute to metabolic acidosis, NAG Hyponatremia (aldosterone failure, non-osmotic ADH release) Salt cravings Hyperkalemia (aldosterone failure)

ACTH 21-hydroxylase deficiency 17 hydroxylase 17-OH Progesterone 21-OH Mini-Aldosterone 11-OH Aldosterone Hypoaldosteronism (Adrenal Insufficiency) Hypotension Hyponatremia (Low aldo/high ADH) Hyperkalemia NAG Metabolic Acidosis What is renin level? elevated (kidney is unaffected by adrenal enyzme deficiency)

CRH If indolent central failure, only cortisol fails. The Renin-Angiotensin-Aldosterone system is intact ACTH Renal (if adrenal failure hypoaldosteronism) Type IV, RTA Failure of aldosterone stimulation of H+-ATPase pump Both contribute to metabolic acidosis, NAG Hyponatremia (aldosterone failure, non-osmotic ADH release) Salt cravings Hyperkalemia (aldosterone failure)

Manifestions of Hypocortisolism Acute, Shock Pituitary Apoplexy Adrenal Hemorrhage HPA Failure Acute cessation+ Signs/symptoms of underlying diseases: HA, diplopia Sepsis, Flank Pain Loss/gain of other hormones (FSH/LH, TSH, Prolactin) Lung cancer, HIV Autoimmune disorders (2) Chronic: HPA axis failure Hypothalamus Infiltrative disorders Pituitary Sheehan s Adenoma/Mass effect Adrenal Autoimmune Infitrative Tumor Infection CAH (enzyme deficiency) HPA Failure Cessation: exogenous CCS

Response to Hypocortisolism (Hypoadrenalism) Acute (adrenal hemorrhage, pituitary apoplexy) Autopsy (too acute but one would predict CRH/ ACTH) Hypothalamic Failure, Exogenous Cessation No CRH no ACTH or cortisol Pituitary Failure (any cause) CRH, ACTH, cortisol CRH Adrenal Failure (e.g. adrenalitis, CAH) CRH, ACTH, cortisol Cortisol ACTH

Hypocortisolism: Diagnostics Clinical Suspicion Hypotension. Low Na, High K, Metabolic Acidosis (NAG), weight loss, [hyperpigmentation, eosinophilia] Labs Random AM cortisol: decreased ACTH stimulation test is gold standard Obtain baseline cortisol level Administer ACTH Check cortisol 30, 60 mins later Normal cortisol level should be >20 mcg/dl or double from baseline ACTH level (should be elevated w/ adrenal failure) If low cortisol and ACTH, central etiology suspected.

Normal adrenal Cortisol Diseased Adrenal (i.e. end organ failure Cortisol No response ACTH Stimulation Test

Loose Ends: Hypocortisolism Exogenous Steroid Cessation Physiologic stress (like going to OR and not getting med) They will describe a patient with a steroid requiring disease such as SLE (they won t tell you the patient is on steroids) They will query you on CRH, ACTH, Cortisol levels May give a CRH stimulation test and ask you the result No pigmentation the HPA axis is suppressed. Autoimmune Adrenalitis Associated with other syndromes such as DM1, pernicious anemia, Hashimoto s just be aware. Atrophy of all 3 layers of the cortex Hypothalamic and Pituitary causes, glomerulosa intact

Loose Ends: Hypocortisolism Exogenous Steroid Cessation Physiologic stress (like going to OR and not getting med) They will describe a patient with a steroid requiring disease such as SLE (they won t tell you the patient is on steroids) They will query you on CRH, ACTH, Cortisol levels May give a CRH stimulation test and ask you the result No pigmentation the HPA axis is suppressed. Autoimmune Adrenalitis Associated with other syndromes such as DM1, pernicious anemia, Hashimoto s just be aware. Atrophy of all 3 layers of the cortex Hypothalamic and Pituitary causes, glomerulosa intact

Sample questions for cortisol dysfunction

A B C D E In the diagram above, choose the appropriate stimulus to hormone release at the region designated by letter E.

A B C D E In the diagram above, choose the appropriate stimulus to hormone release at the region designated by letter E. A Capsule B- Glomerulosa C Fasciculata D Reticularis E - Medulla What type of cells are present in the adrenal medulla?

A B C D E In the diagram above, choose the appropriate stimulus to hormone release at the region designated by letter E. A Capsule B- Glomerulosa C Fasciculata D Reticularis E - Medulla Postganglionic sympathetic neurons. What stimulates hormonal release?

A B C D E In the diagram above, choose the appropriate stimulus to hormone release at the region designated by letter E. A Capsule B- Glomerulosa Renin ATII Aldosterone; Hyperkalemia C Fasciculata - ACTH D Reticularis - ACTH E Medulla: Answer - Ach

Patient has SLE using medicine to treat the condition. Noted with truncal obesity, hirsutism, facial plethora. She complains of proximal muscle weakness. Labs reveal an elevated glucose. She dies suddenly. How does the adrenal appear histologically? A. Atrophy of three cortical layers B. Atrophy of two cortical layers C. Hyperplasia of two cortical layers D. Hyperplasia of three cortical layers

Patient has SLE using medicine to treat the condition. Noted with truncal obesity, hirsutism, facial plethora. She complains of proximal muscle weakness. Labs reveal an elevated glucose. She dies suddenly. How does the adrenal appear histologically? A. Atrophy of three cortical layers B. Atrophy of two cortical layers C. Hyperplasia of two cortical layers D. Hyperplasia of three cortical layers They continue to push the point that Aldosterone secretion and the Glomerulosa are ACTH independent

Patient has SLE using medicine to treat the condition. Noted with truncal obesity, hirsutism, facial plethora. She complains of proximal muscle weakness. Labs reveal an elevated glucose. She dies suddenly. Describe the levels of hormones at the time of her death. A. A A. B. B B. C. C C. D. D D. E. E E. F. F F.

Patient has SLE using medicine to treat the condition. Noted with truncal obesity, hirsutism, facial plethora. She complains of proximal muscle weakness. Labs reveal an elevated glucose. She dies suddenly. Describe the levels of hormones at the time of her death. A. A A. B. B B. C. C C. D. D D. E. E E. F. F F.

60 yo with difficulty climbing stairs and dyspnea. Wt gain over several months. CXR lung mass. Labs with high cortisol and ACTH. Next diagnostic study? A. Chest CT scan B. MRI of Pituitary C. Dexamethasone suppression test D. Echocardiography E. CPK level

60 yo with difficulty climbing stairs and dyspnea. Wt gain over several months. CXR lung mass. Labs with high cortisol and ACTH. Next diagnostic study? A. Chest CT scan B. MRI of Pituitary C. Dexamethasone suppression test D. Echocardiography E. CPK level

60 yo with difficulty climbing stairs and dyspnea. Wt gain over several months. CXR lung mass. Labs with high cortisol and ACTH. Next diagnostic study? A. Chest CT scan B. MRI of Pituitary C. Dexamethasone suppression test D. Echocardiography E. CPK level

60 yo with difficulty climbing stairs and dyspnea. Wt gain over several months. CXR lung mass. Labs with high cortisol and ACTH. Next diagnostic study? A. Chest CT scan B. MRI of Pituitary C. Dexamethasone suppression test D. Echocardiography E. CPK level

Woman with wt loss. PE muscle wasting with 4/5 strength bilaterally. CT reveals enlarged adrenal glands. CXR shows prominent hilar mass. Labs: Na+ 120; K+ 6.0; HCO3 21. 8 AM Cortisol is 4 ng/ml (normal >5). What test would be confirmatory? A. ACTH level B. Dexamethasone suppression C. ACTH stimulation test D. Chest CT scan

Woman with wt loss. PE muscle wasting with 4/5 strength bilaterally. CT reveals enlarged adrenal glands. CXR shows prominent hilar mass. Labs: Na+ 120; K+ 6.0; HCO3 21. 8 AM Cortisol is 4 ng/ml (normal >5). What test would be confirmatory? A. ACTH level B. Dexamethasone suppression C. ACTH stimulation test D. Chest CT scan

Adrenal Disorders for the USMLE, Step One: Abnormalities of the Fasciculata The Official Winter Storm of the Class of 2019