JACK L. SNITZER, DO INTERNAL MEDICINE BOARD REVIEW COURSE 2018 PITUITARY

Similar documents
PITUITARY: JUST THE BASICS PART 2 THE PATIENT

Pathology of pituitary gland. By: Shifaa Qa qa

Pituitary Adenomas: Evaluation and Management. Fawn M. Wolf, MD 10/27/17

Kingdom of Bahrain Arabian Gulf University College of Medicine and Medical Sciences. Endocrinology. (Review) Year 5 Internal Medicine

Diseases of pituitary gland

Pituitary Gland Disorders

Mechanism of hyperprolactinemia

What we will cover. Evaluation of the Child with Suspected Pituitary Disease. ituitary

Hypothalamus & Pituitary Gland

panhypopituitarism Pattawan Wongwijitsook Maharat Nakhon Ratchasima hospital 17 Nov 2013

PATIENT INFORMATION HYPOPITUITARISM YOUR QUESTIONS ANSWERED

Functional Pituitary Adenomas. Fawn M. Wolf, MD 2/2/2018

GLMS CME- Cell Group 5 10 April Greenlane Medical Specialists Pui-Ling Chan Endocrinologist

HYPOTHALAMO PITUITARY GONADAL AXIS

Endocrine part two. Presented by Dr. Mohammad Saadeh The requirements for the Clinical Chemistry Philadelphia University Faculty of pharmacy

Introduction to Endocrinology. Hypothalamic and Pituitary diseases Prolactinoma + Acromegaly

Pituitary for the General Practitioner. Marilyn Lee Consultant physician and endocrinologist

Peri-op Pituitary / Diabetes Insipidus/ Apoplexy Dr. Stan Van Uum, MD, PhD, FRCPC

Endocrinological Outcome Among Treated Craniopharyngioma Patients

Mineralocorticoids: aldosterone Angiotensin II/renin regulation by sympathetic tone; High potassium will stimulate and ACTH Increase in aldosterone

Pituitary Disorders. Eiman Ali Basheir Mob: /1/2019

(3) Pituitary tumours

Urgent and Emergent Pituitary Conditions

ABNORMAL PITUITARY FUNCTION

Evaluation and Management of Pituitary Failure. Dr S. Ali Imran MBBS, FRCP (Edin), FRCPC Professor of Medicine Dalhousie University, Halifax, NS

THE ANTERIOR PITUITARY. Embryology cont. Embryology of the pituitary BY MISPA ZUH HS09A179. Embryology cont. THE PITUIYARY GLAND Anatomy:

Hormones by location

John Sutton, DO, FACOI, FACE, CCD. Carson Tahoe Endocrinology Carson City, NV KCOM Class of 1989

Hormonal Replacement in Hypopituitarism in Adults: An Endocrine Society Clinical Practice Guideline

Pituitary Disorders Suranut Charoensri, MD

Pituitary gland diseases

Imaging pituitary gland tumors

By: Mohammad Jomaa & Amer Al-Salamat. Lec:Pathology of pituitary gland. **Sheet contain the slide in Bold. **some book information in Red.

MANAGEMENT OF PATIENTS WITH PITUITARY DISORDERS ON THE NEUROSUGERY WARDS RESPONSIBILITIES OF THE METABOLIC REGISTRAR

Neuroendocrine Disorders in Women

4.04 Understand the Functions and Disorders of the ENDOCRINE SYSTEM Understand the functions and disorders of the endocrine system

Sharon maslovitz Lis Maternity Hospital

Medical and Rehabilitation Innovations Neuroendocrine Screening and Hormone Replacement Therapy in Trauma Related Acquired Brain Injury

Case Report Rapid Pituitary Apoplexy Regression: What Is the Time Course of Clot Resolution?

Pituitary Disease Resident Tutorial 2017

33-Year-Old Female With Amenorrhea DISHA KUMAR NARANG, MD PITUITARY ENDORAMA DECEMBER 11, 2014

Prepared By Margaret May RN MSN Fall 2016 Nursing 200

I. Provide patient care that is compassionate, appropriate and effective for the prevention and treatment of endocrinologic disorders.

Pituitary Tumors and Incidentalomas. Bijan Ahrari, MD, FACE, ECNU Palm Medical Group

Pituitary Apoplexy. Updated: April 22, 2018 CLINICAL RECOGNITION

Diseases of the Adrenal gland

Pathophysiology of Pituitary Gland Disorders. PHCL 415 Hadeel Alkofide May 2010

Professor Ian Holdaway. Endocrinologist Auckland District Health Board

Chapter 12 Endocrine System (export).notebook. February 27, Mar 17 2:59 PM. Mar 17 3:09 PM. Mar 17 3:05 PM. Mar 17 3:03 PM.

See the latest estimates for new cases of pituitary tumors in the US and what research is currently being done.

Take Home Messages in Endocrinology

CYSTIC PROLACTINOMA: A SURGICAL DISEASE?

Clinical presentations of endocrine diseases

Pharmacology of Hypothalamic Hormones

Biology 30. Morinville Community High School. Unit 2: Endocrine System. Name:

Adrenal Gland Disorders

Reproductive Health and Pituitary Disease

Case Report Successful Pregnancy in a Female with a Large Prolactinoma after Pituitary Tumor Apoplexy

Endocrine system overview

Challenging Pituitary Cases. Laurence Katznelson, MD Professor of Medicine and Neurosurgery Stanford University School of Medicine

DIMENSIONS 1 cm in diameter 0.5 to 1 gm in weight. LOCATION Sella turcica A bony cavity. DIVISIONS Anterior lobe Posterior lobe Pars intermedia

WARD INSTRUCTIONS WEBSITE

Pituitary Tumors: adenoma, craniopharyngioma, rathke cyst

62-year-old woman with severe headache. Celeste Thomas November 1, 2012

CATEGORY Endocrine System Review. Provide labels for the following diagram CHAPTER 13 BLM

The Endocrine System Dr. Gary Mumaugh

Endocrine Testing. Alice Y.Y. Cheng, MD, FRCP October 14, 2015

Initials:.. Number of patient in the registry:... Date of visit:.. Gender (genetic): female / male

Hyperprolactinemia: N hidshi i MD. Nahid Shirazian MD. Internist, Endocrinologist

HYPOPITUITARISM. Partial or complete loss of production of one or more of the pituitary gland hormones. Diagnosis Male & Female

The Endocrine System. Lipid-Soluble Hormones. Bio217 Sp14 Unit 5. Bio217: Pathophysiology Class Notes Professor Linda Falkow

CCRN/PCCN Review Course May 30, 2013

Endocrine System. The Endocrine Glands

Robert Wadlow and his father

Ch 8: Endocrine Physiology

Imaging The Turkish Saddle. Russell Goodman, HMS III Dr. Gillian Lieberman

Secondary amenorrhoea Dr.ASMAA AL SANJARY

Antidiuretic Hormone

Leticia Hernández Dávila, MD May 26, J Clin Endocrinol Metab (2016) 101 (11):

Pituitary apoplexy 台北榮總內分泌新陳代謝科主治醫師林怡君

Neuroendocrine challenges following hemispherectomy

UW MEDICINE PATIENT EDUCATION. Acromegaly Symptoms and treatments. What is acromegaly? DRAFT. What are the symptoms? How is it diagnosed?

ENDOCRINOLOGY COORDINATION OF PHYSIOLOGICAL PROCESSES:

AUGUST 25-27, 2017 UPDATE & BOARD REVIEW. acofp INTENSIVE. Evolving Issues in Endocrinology. Chris Pitsch, DO INNOVATIVE COMPREHENSIVE HANDS-ON

Subject Index. hypothalamic-pituitary-adrenal axis 158. Atherosclerosis, ghrelin role AVP, see Arginine vasopressin.

Prolactin-Secreting Pituitary Adenomas (Prolactinomas) The Diagnostic Pathway (11-2K-234)

Endocrine part one. Presented by Dr. Mohammad Saadeh The requirements for the Clinical Chemistry Philadelphia University Faculty of pharmacy

Disclosures. BMS, Ferring research grant funding NovoNordisk scientific advisory board Chiasma clinical trial investigator

Pituitary Stalk Interruption Syndrome. Leena Shahla, MD, PGY5 Endocrinology, Diabetes and Metabolism Fellowship University of Massachusetts

Chapter 43. Endocrine System. Negative Feedback. Hypothalamus and Pituitary Glands

The Investigations of the Pituitary Gland

PITUITARY ADENOMA HORMONAL AND MEDICAL MANAGEMENT

Endocrine System. Modified by M. Myers

Spontaneous remission of acromegaly and Cushing s disease following pituitary apoplexy: Two case reports

Hyperprolactinemia. Justin Moore, MD

PROBLEMS WITH REGULATION AND METABOLISM. Objectives A & P 8/11/2011

Describe the epidemiology and clinical presentations of pituitary tumours:

9.2: The Major Endocrine Organs

Metoclopramide Domperidone. HYPER- PROLACTINAEMIA: the true and the false problems

Transcription:

JACK L. SNITZER, DO INTERNAL MEDICINE BOARD REVIEW COURSE 2018 PITUITARY

JACK L. SNITZER, D.O. Peninsula Regional Endocrinology 1415 S. Division Street Salisbury, MD 21804 Phone:410-572-8848 Fax:410-572-6890 E-Mail: DSNITZER1@COMCAST.NET

DISCLOSURES Speaker bureau for: BI-Lilly Janssen

-Anterior l l l l l l PITUITARY Thyroid Stimulating Hormone (TSH) Prolactin (PRL) Growth Hormone (GH) Corticotropin (ACTH) Luteinizing Hormone (LH) Follicle Stimulating Hormone (FSH) -Posterior (hormones made in the hypothalamus and stored in pituitary) l l Vasopressin Oxytocin

PITUITARY TUMORS -Tumors-usually benign adenomas Common tumors, 70-80% are functional Microadenoma:<1cm; macroadenoma:1+ cm can classically cause l bitemporal hemianopsia l hypopituitarism l headaches l amenorrhea l galactorrhea l growth/puberty delay l infertility l decreased libido/erectile dysfunction

PITUTARY TUMORS If suspected or being followed, order MRI of head attn: sella with and without contrast Note: CT scans might miss pituitary tumors; general head MRI s that are not specifically ordered with pituitary (sella) protocol might miss small pituitary tumors.

PITUITARY TUMORS All pituitary tumors require testing for hormonal hyper-secretion and pituitary insufficiency. Visual fields must be checked if tumor is large and follow-up MRI obtained. Surgery usually recommended if visual field defects (impingement of the tumor on the optic chiasm), unless a prolactinoma, or significant growth of a large tumor.

NON-SECRETORY PITUITARY Non-secretory tumors TUMORS - Can be incidental microadenomas. - Can be large and might cause partial or full hypopituitarism and visual field defects. Symptoms of pituitary insufficiency might be present or might be minimal or absent, until the patient is under stress, when severe adrenal insufficiency might occur.

PROLACTINOMA -Prolactinoma galactorrhea, infertility, amenorrhea, decreased libido; can cause hypogonadism in females or males. (note: prolactin elevation is generally proportional to size of tumor)

PROLACTINOMA Treatment Cabergoline (Dostinex) twice weekly (more effective than bromocriptine and better tolerated generally); side effects: nausea, dizzy; long-term at high doses: pulmonary fibrosis. Ergotamine syndrome. Bromocriptine (Parlodel) nightly; side effects: nausea, dizzy. rarely surgery

PROLACTIN ELEVATION Other Causes of mildly elevated prolactin - Dopamine antagonists - metoclopramide - many anti-psychotics (haldol, risperidone) - pituitary stalk compression from pituitary macroadenomas or non-pituitary tumors - Nipple stimulation - Caffeine

ACROMEGALY -Acromegaly: growth hormone (GH) excess - Signs/Symptoms: doughy and large hands, increasing hand and foot size, large tongue, frontal bossing, prominent chin, increased cardiovascular mortality. - Lab: high IGF-1 level (and GH level although don t need to check GH level); might have deficits of other pituitary hormones

ACROMEGALY Generally a large pituitary tumor Check IGF-1 level (Insulin-like Growth Factor- 1) Glucose tolerance test to see if GH level suppresses. TREATMENT 1. Surgery; 2. possibly octreotide or pegvisomant; 3. possibly radiation therapy

ACROMEGALY

TSH secreting tumor TSH secreting tumor- rare (central hyperthyroidism). -elevated TSH and free T4 and often hyperthyroid symptoms. (note: in a patient with chronic poorly treated hypothyroidism, there might be significant pituitary thyrotroph hyperplasia noted on MRI. However, the TSH in this case will be high and the free T4 usually very low and the thyrotroph hyperplasia often resolves with adequate thyroxine treatment)

CUSHING S DISEASE -Cushing's Disease-ACTH secretion (ACTH dependent). obesity, striae, ecchymoses, hyperglycemia, atherosclerosis, thin skin, fatigue, fat pads (especially supraclavicular), hyperpigmentation, infections

CUSHING S DISEASE Diagnosis l l l l 24 hour urine free cortisol. dexamethasone suppression test Salivary cortisol between 11 pm and midnight Tests might need to be repeated, especially if subtle cortisol excess Treatment l surgery, might then need radiation

CUSHING S DISEASE

Dexamethasone suppression testing Low dose overnight: 1 mg dexamethasone at 11 pm. Fasting cortisol the next AM at 8AM. Normal result is suppression of cortisol to <2-3 mcg/dl. (<2 is more definitive) If abnormal, indicates possibility of cortisol excess and further testing is needed. Note: obtaining a baseline ACTH level (without suppression) at some point might be helpful in patients who end up having abnormal low dose suppression testing. This can help us differentiate ACTH dependent vs. ACTH independent Cushing s.

Dexamethasone suppression testing High dose overnight suppression testing: Obtain baseline cortisol level and ACTH. Give 8 mg dexamethasone at 11 pm. Fasting cortisol level the next AM at 8 AM. Normal is a >50% reduction in cortisol.

Dexamethasone suppression testing INTERPRETATION Adrenal Cushing s syndrome: failure to suppress cortisol with low dose dexamethasone testing and low ACTH level at baseline. Usually don t need high dose dexamethasone test.

Dexamethasone suppression testing INTERPRETATION Pituitary Cushing s disease (ACTH dependent Cushing s): failure to suppress cortisol with low dose dexamethasone test. Adequate suppression with high dose dexamethasone test generally. Elevated or normal ACTH level at baseline.

Dexamethasone suppression testing INTERPRETATION Ectopic ACTH: Failure to suppress cortisol with low dose and high dose dexamethasone suppression. High baseline ACTH level. Often metabolic alkalosis and hypokalemia.

EMPTY SELLA Fairly common. Often asymptomatic but can have partial or pan-hypopituitarism. Might be due to invagination of CSF into the sella, compressing the sella; pituitary infarction; etc.

Sellar extension of non-pituitary tumors -Sellar extension of non-pituitary tumors might cause elevated prolactin; Might cause diabetes insipidus by stalk compression; might cause visual field defects; might cause pituitary insufficiency.

DIABETES INSIPIDUS loss of vasopressin secretion (central DI) Complete or Partial DI Inability to concentrate urine Hypernatremia, dehydration, elevated serum osmolality (note: some patients with partial DI and intact thirst mechanisms can drink enough fluid to maintain normal sodium levels) urine osmolality less than 290 with elevated serum osmolality Generally have frequent urination

DIABETES INSIPIDUS Confirmation if needed: Water deprivation test (cautiously)

DIABETES INSIPIDUS -Diabetes Insipidus (cont) Treatment l Replete fluids to correct serum sodium l DDAVP (desmopressin) - IV, SQ, Nasal spray, oral: initiate when sodium level is rising or in the 140 range or higher. Note: treatment with DDAVP might be needed based on hypernatremia and/or to improve urinary frequency; fluid intake will have to be adjusted based on the effect of the DDAVP

DIABETES INSIPIDUS Must adjust the fluid intake and DDAVP together to avoid excessive fluid retention from DDAVP (and resultant hyponatremia), especially in a head trauma patient with cerebral edema. Also important in a patient with lack of thirst mechanism. The maintenance dose of DDAVP will likely depend on the sodium level and convenience related to frequency of urination and amount of fluid a patient can take in.

OTHER PITUITARY ISSUES -Head irradiation can cause hypopituitarism years later -Sheehan's Syndrome post-partum pituitary necrosis; usually due to infarction of a pituitary adenoma during a difficult delivery with hypotension. -Hemorrhage -Hypothalamic Dysfunction -Infiltrative Disease -Autoimmune hypophysitis

HYPOPITUITARISM -Hypopituitarism - Flu-like symptoms Urgent diagnosis Glucocorticoid replacement (Hydrocortisone 10-20 mg in am and 5-10 mg in pm with food, prednisone 5-7.5 mg daily, or equivalent) Consider testosterone/estrogen replacement levothyroxine replacement (TSH level not useful in determining dose since pituitary can t make TSH adequately) might need DDAVP, growth hormone

HYPOPITUITARISM HYPOPITUITARISM Dx: - Symptoms (flu-like: nausea, dizziness, achiness, etc.) - Low FSH in post-menopausal woman not on estrogen - Low total and free testosterone and LH in males - Low sodium possibly -possibly low morning cortisol (not a sensitive test) or and abnormal ACTH stimulation test (unless it is recent pituitary insufficiency) - low TSH and low free T4; or low free T4 and inappropriately normal TSH.

CASE 1-35 year old, recent post-partum female. Treated with clomiphene for infertility. Hypotensive during delivery. Orthostatic, hyponatremia. Past history of oligomenorrhea, galactorrhea.

CASE 1 Sheehan syndrome. She likely had a pituitary adenoma (possibly a prolactinoma, which grew during pregnancy and infarcted when she became hypotensive during delivery)

CASE 2-60 year old centrally obese patient, 80 pound weight increase in one year. Type 2 diabetes mellitus for 3 years. Tanned skin. Leg weakness. Violaceous new stretch marks.

CASE 2 Type 2 diabetes mellitus versus Cushing s syndrome. Obtain overnight 1 mg dexamethasone suppression test and/or 24 hour urine free cortisol (and/or midnight salivary cortisol)

CASE 3-34 year old head trauma victim. Polyuria while IV fluids infusing. On dexamethasone. Serum sodium:168. Confused.

CASE 3 Needs DDAVP since has DI and sodium level is high. Notes: IV fluids can cause polyuria as can postoperative diuresis. Dexamethasone (glucocorticoids) can exacerbate diabetes insipidus.

CASE 3 What if this patient s sodium level was 135? Then wouldn t give DDAVP since this would cause fluid retention and hyponatremia. Adjust fluids to urine output and hold off on DDAVP until sodium level is perhaps in the low 140 s, then can start DDAVP. Adjust fluids and DDAVP to prevent fluid overload and to maintain serum sodium level in the normal range. This patient might not even have DI.