(Ebook PDF) Adrenal Disorders Cases from the Adrenal Clinic 1st edition by William Young, Irina Bancos ISBN 9780323792875 0323792871 full chapters

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ISBN 10:0323792871

ISBN 13:9780323792875

Author: William F. Young; Irina Bancos

Adrenal disorders are often difficult to diagnose due to common symptoms, and challenging to treat due to common comorbidities. Adrenal Disorders: 100 Cases from the Adrenal Clinic provides a comprehensive, case-based approach to the evaluation and treatment of both common and uncommon adrenal disorders, offering practical, real-world guidance highlighted by ultrasound scans, biopsy images, and tables.

• Features 100 two-page cases covering a wide range of common and uncommon adrenal disorders. 

• Includes , investigations, treatment, and outcome for each case, plus a case overview with expert advice, take-home points, and . 

• Organizes comprehensive content by type of disorder, including adrenal masses (benign and malignant), primary aldosteronism, ACTH-independent Cushing syndrome, ACTH-dependent Cushing syndrome, adrenal carcinoma, and pheochromocytoma. 

Table of Contents:

Section A Incidentally DiscoveredAdrenal Mass

• Case 1 45-Year-Old Woman With an Incidentally Discovered Large Adrenal Mass
• Treatment
• Case 2 Adrenal Mass in a Patient With History of Extraadrenal Malignancy: The Role of Imaging
• Case 3 Incidentally Discovered Adrenal Mass in a Patient With History of Extraadrenal Malignancy: The Role of Adrenal Biopsy
• Case 4 Nonfunctioning Lipid Rich Adrenocortical Adenoma: Role of Follow-Up
• Case 5 54-Year-Old Woman With an Incidentally Discovered Adrenal Mass and Abnormal Dexamethasone Suppression Test: Role of Adrenalectomy
• Case 6 Lipid-Poor Adrenal Masses: The Case for Aggressive Management

Section B Primary Aldosteronism

• Case 7 Primary Aldosteronism: When Adrenal Venous Sampling Is Not Needed Before Unilateral Adrenalectomy
• Case 8 Primary Aldosteronism With Unilateral Adrenal Nodule on Computed Tomography
• Case 9 Primary Aldosteronism With Bilateral Adrenal Nodules on Computed Tomography
• Case 10 Primary Aldosteronism Caused by Unilateral Adrenal Hyperplasia
• Case 11 Primary Aldosteronism in a Patient With Bilateral Macronodular Adrenal Hyperplasia and Associated Clinically Important Cortisol Cosecretion
• Case 12 Primary Aldosteronism in a Patient With an Adrenal Macroadenoma and Clinically Important Cortisol Cosecretion
• Case 13 Primary Aldosteronism in a Patient Treated With Spironolactone
• Case 14 Failed Catheterization of the Right Adrenal Vein: When Incomplete Adrenal Venous Sampling Data Can Be Used to Direct a Surgical Cure
• Case 15 Primary Aldosteronism: When Adrenal Venous Sampling Shows Suppressed Aldosterone Secretion From Both Adrenal Glands

Section C Corticotropin-Independent Cushing Syndrome

• Case 16 28-Year-Old Woman With Remote History of Adrenal Mass Presenting With New-Onset Hypertension and Weight Gain
• Case 17 26-Year-Old Woman With a Discrepant Workup for Cushing Syndrome Subtype
• Case 18 45-Year-Old Woman With Corticotropin-Independent Cushing Syndrome and Bilateral Adrenal Adenomas
• Case 19 Corticotropin-Independent Cushing Syndrome in a Patient With “Normal” Adrenal Imaging
• Case 20 66-Year-Old Woman With Corticotropin-Independent Hypercortisolism and Bilateral Macronodular Adrenal Hyperplasia
• Case 21 35-Year-Old Woman With Low Bone Density and Fractures
• Case 22 Carney Triad (Pentad) and Adrenal Adenoma With Clinically Important Cortisol Secretory Autonomy

Section D Adrenal Cortical Carcinoma and Oncocytic Neoplasm

• Case 23 Adrenal Cortical Carcinoma in a Patient With a History of Adrenal Incidentaloma
• Case 24 Unexpected Diagnosis of Adrenal Cortical Carcinoma: Role of Urinary Steroid Profiling
• Case 25 Oncocytic Adrenocortical Carcinoma
• Case 26 Mitotane Therapy in the ENSAT Stage II Adrenocortical Carcinoma
• Case 27 Cortisol-Secreting Metastatic Adrenocortical Carcinoma: Role for Surgical Debulking of the Primary Tumor
• Case 28 Adrenocortical Carcinoma and Severe Cushing Syndrome
• Case 29 Pure Aldosterone-Secreting Adrenocortical Carcinoma
• Case 30 Long-Standing Primary Aldosteronism in a Patient Diagnosed With Metastatic Adrenocortical Carcinoma
• Case 31 Adrenocortical Carcinoma Associated With Lynch Syndrome
• Case 32 Adrenocortical Carcinoma Associated With Multiple Endocrine Neoplasia Type 1
• Case 33 Adrenocortical Carcinoma Presenting With Inferior Vena Cava Thrombus
• Case 34 Management of Mitotane Therapy in Adrenocortical Carcinoma

Section E Pheochromocytoma and Paraganglioma

• Case 35 Most Pheochromocytomas Grow Slowly
• Case 36 The “Prebiochemical” Pheochromocytoma
• Case 37 Huge Catecholamine-Secreting Tumor
• Case 38 Metyrosine Use in a Patient With Metastatic Pheochromocytoma
• Case 39 Pheochromocytoma in a Patient With Neurofibromatosis Type 1
• Case 40 New Diagnosis of Multiple Endocrine Neoplasia Type 2A in a Patient With Bilateral Pheochromocytomas
• Case 41 Pheochromocytoma in a Patient With von Hippel Lindau Disease
• Case 42 Bilateral Pheochromocytoma in a Patient With MYC-Associated Protein X (MAX) Genetic Predisposition
• Case 43 The Cystic Pheochromocytoma
• Case 44 Skull Base and Neck Paragangliomas: Considerations for the Endocrinologist
• Case 45 Cardiac Paraganglioma
• Case 46 Pheochromocytoma in Multiple Endocrine Neoplasia Type 2B
• Case 47 Metastatic Paraganglioma: An Approach to Management and the Use of Serial Imaging to Assess the Rate of Tumor Progression
• Case 48 Metastatic Pheochromocytoma: Role for Ga-68 DOTATATE PET-CT
• INVESTIGATIONS
• Case 49 Carney Triad (Pentad) and Catecholamine-Secreting Paragangliomas
• Case 50 Metastatic Paraganglioma: Role for Systemic Chemotherapy
• Case 51 Cryoablation Therapy for Metastatic Paraganglioma
• Case 52 Paraganglioma in a Patient With Cyanotic Cardiac Disease
• Case 53 Metastatic Paraganglioma—Role for External Beam Radiation Therapy

Section F Corticotropin-Dependent Hypercortisolism

• Case 54 Corticotropin-Dependent Cushing Syndrome Can Be Frequently Misdiagnosed
• Case 55 Corticotropin-Dependent Cushing Syndrome: Role for Inferior Petrosal Sinus Sampling
• Case 56 Corticotropin-Dependent Cushing Syndrome: When Inferior Petrosal Sinus Sampling Is Not Needed
• Case 57 Severe Corticotropin-Dependent Cushing Syndrome From a Pituitary Adenoma
• Case 58 Ectopic Cushing Syndrome Associated With Multiple Endocrine Neoplasia Type 2B
• Case 59 Ectopic Cushing Syndrome Treated With Cryoablation
• Case 60 Cyclical Ectopic Cushing Syndrome
• Treatment
• Case 61 Mild Cushing Syndrome Associated With Ectopic Corticotropin Secretion
• Case 62 Bilateral Adrenal Cryoablation in Corticotropin-Dependent Cushing Syndrome
• Case 63 Cushing Syndrome Associated With Ectopic Corticotropin and Corticotropin-Releasing Hormone–Secreting Pheochromocytoma
• Case 64 Cushing Syndrome in the Setting of Multiple Endocrine Neoplasia Type 1

Section G Other Adrenal Masses

• Case 65 Adrenal Myelolipoma: A Computed Tomography Diagnosis
• Case 66 Adrenal Schwannoma
• Case 67 Trauma-Related Unilateral Adrenal Hemorrhage
• Case 68 Bilateral Adrenal Hemorrhage
• Case 69 Primary Adrenal Teratoma
• Case 70 The Adrenal Stone
• Case 71 Simple Adrenal Cyst
• Case 72 Adrenal Cystic Lymphangioma
• Case 73 Adrenal Hemangioma
• Case 74 Adrenal Ganglioneuroma
• Case 75 42-Year-Old Woman With a Large Composite Adrenal Mass
• Case 76 Primary Adrenal Leiomyosarcoma
• Case 77 Primary Adrenal Lymphoma
• Case 78 39-Year-Old Man With a Large Adrenal Mass
• Case 79 59-Year-Old Man With Enlarging Bilateral Adrenal Masses
• Case 80 65-Year-Old Man With Primary Adrenal Insufficiency
• Case 81 47-Year-Old Man With Primary Adrenal Insufficiency
• Case 82 Bilateral Adrenal Myelolipoma: Think of Congenital Adrenal Hyperplasia
• Case 83 A Unilateral Lipid-Poor Adrenal Mass: An Atypical Presentation of Adrenal Histoplasmosis
• Case 84 Bilateral Macronodular Adrenal Hyperplasia in the Setting of Multiple Endocrine Neoplasia Type 1
• Case 85 Pseudo-Adrenal Masses

Section H Adrenal and Ovarian Hyperandrogenism

• Case 86 A Huge Adrenal Myelolipoma in a Patient With a Suboptimally Controlled Congenital Adrenal Hyperplasia
• Case 87 Balancing Glucocorticoid and Androgen Excess in Congenital Adrenal Hyperplasia
• Case 88 Dehydroepiandrosterone Sulfate: The “Love It” or “Hate It” Hormone
• Reference
• Case 89 Sorting Out the Source of Androgen Excess in a Postmenopausal Woman With an Adrenal and an Ovarian Mass
• Case 90 Primary Testosterone-Secreting Adrenocortical Carcinoma in a Premenopausal Woman
• Case 91 Premenopausal Woman With Testosterone-Secreting Ovarian Tumor
• Case 92 Sorting Out the Source of Androgen Excess in a Postmenopausal Woman With an Adrenal Mass
• Case 93 Testosterone-Secreting Benign Adrenal Adenoma in a Postmenopausal Woman

Section I Adrenal Disorders in Pregnancy

• Case 94 Malignant Pheochromocytoma in Pregnancy
• Case 95 Catecholamine-Secreting Paraganglioma in Pregnancy
• Case 96 The Peripartum Diagnosis of Pheochromocytoma and a Genetic Mystery Solved
• Case 97 History of Pregnancy in a 41-Year-Old Woman With Undiagnosed Cushing Syndrome
• Case 98 Pregnancy in a Patient With Primary Adrenal Insufficiency
• Case 99 Pregnancy in a Patient With 21-Hydroxylase Deficiency
• Case 100 Primary Aldosteronism in Pregnancy

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