의학서적전문 "성보의학서적"의 신간의학도서입니다.

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.

Key Features

•Features 100 two-page cases covering a wide range of common and uncommon adrenal disorders.
•Includes case report, investigations, treatment, and outcome for each case, plus a case overview with expert advice, take-home points, and references.
•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.
•Enhanced eBook version included with purchase. Your enhanced eBook allows you to access all of the text, figures, and references from the book on a variety of devices.

Author Information

By William F. Young, Jr., MD, Division of Endocrinology, Diabetes, Metabolism, and Nutrition, Tyson Family Endocrinology Clinical Professor; Professor of Medicine, Mayo Clinic College of Medicine and Irina Bancos, MD, Associate Professor, Division of Endocrinology and Metabolism at the Mayo Clinic, Rochester, Minnesota

-도서목차-

 Incidentally Discovered Adrenal Mass
1 Case #1. 45-Year Old Woman with an Incidentally Discovered Large Adrenal Mass
2 Case #2: Adrenal Mass in a Patient with History of Extra-adrenal Malignancy: the Role of Imaging
3 Case #3: Incidentally Discovered Adrenal Mass in a Patient with History of Extra-adrenal Malignancy: the Role of Adrenal Biopsy
4 Case #4: Nonfunctioning Lipid Rich Adrenocortical Adenoma—Role of Follow-up
5 Case #5:54-Year Old Woman with an Incidentally Discovered Adrenal Mass and Abnormal Dexamethasone Suppression Test: Role of Adrenalectomy
6 Case #6: Lipid Poor Adrenal Masses—The Case for Aggressive Management
 INTRODUCTION with basics of diagnosis and work up ( 1-2 pages) WFY
 Primary Aldosteronism
7 Case #7: Primary Aldosteronism—When Adrenal Venous Sampling is not Needed Before Unilateral Adrenalectomy
8 Case #8: Primary Aldosteronism with Unilateral Adrenal Nodule on Computed Tomography
9 Case #9: Primary Aldosteronism with Bilateral Adrenal Nodules on Computed Tomography
10 Case #10: Primary Aldosteronism Caused by Unilateral Adrenal Hyperplasia
11 Case #11: Primary Aldosteronism in a Patient with Bilateral Macronodular Adrenal Hyperplasia and Associated Clinically Important Cortisol Co-secretion
12 Case #12: Primary Aldosteronism in a Patient with an Adrenal Macroadenoma and Clinically Important Cortisol Co-secretion
13 Case #13: Primary Aldosteronism in a Patient Treated with Spironolactone
14 Case #14: Failed Catheterization of the Right Adrenal Vein—When Incomplete Adrenal Venous Sampling Data Can Be Used to Direct a Surgical Cure
15 Case #15: Primary Aldosteronism: When Adrenal Venous Sampling Shows Suppressed Aldosterone Secretion From Both Adrenal Glands
 ACTH-Independent Cushing Syndrome
16 Case #16: 28-Year-Old Woman with Remote History of Adrenal Mass Presenting with New Onset Hypertension and Weight Gain
17 Case #17: 26-Year-Old Woman with a Discrepant Work-up for Cushing Syndrome Subtype
18 Case #18: 45-Year-Old Woman with Corticotropin-Independent Cushing Syndrome and Bilateral Adrenal Adenomas
19 Case #19: Corticotropin-Independent Cushing Syndrome in a Patient with “Normal” Adrenal Imaging
20 Case #20:66-Year-Old Woman with Corticotropin-Independent Hypercortisolism and Bilateral Macronodular Adrenal Hyperplasia
21 Case #21: 35-Year-Old Woman with Low Bone Density and Fractures
22 Case #22: Carney Triad (Pentad) and Adrenal Adenoma with Clinically Important Cortisol Secretory Autonomy
 Adrenal Cortical Carcinoma and Oncocytic Neoplasm
23 Case #23: Adrenal cortical carcinoma in a patient with history of adrenal incidentaloma
24 Case #24: Unexpected Diagnosis of Adrenal Cortical Carcinoma: Role of Urinary Steroid Profiling
25 Case #25: Oncocytic adrenocortical carcinoma
26 Case #26:Mitotane therapy in the ENSAT Stage II Adrenocortical Carcinoma
27 Case #27: Cortisol-Secreting Metastatic Adrenocortical Carcinoma—Role for Surgical Debulking of the Primary Tumor
28 Case #28:Adrenocortical Carcinoma and Severe Cushing Syndrome
29 Case #29: Pure Aldosterone-Secreting Adrenocortical Carcinoma
30 Case #30:Long-standing Primary Aldosteronism in a Patient Diagnosed with Metastatic Adrenocortical Carcinoma
31 Case #31: Adrenocortical Carcinoma Associated with Lynch Syndrome
32 Case #32: Adrenocortical Carcinoma Associated with Multiple Endocrine Neoplasia Type 1
33 Case #33: Adrenocortical Carcinoma Presenting with Inferior Vena Cava Thrombus
34 Case #34: Management of Mitotane Therapy in Adrenocortical Carcinoma
 E. Pheochromocytoma and Paraganglioma
35 Case #35: Most Pheochromocytomas Grow Slowly
36 Case #36: The “Prebiochemical” Pheochromocytoma
37 Case #37: Huge Catecholamine-Secreting Tumor
38 Case#38: Metyrosine Use in a Patient with Metastatic Pheochromocytoma
39 Case #39:Pheochromocytoma in a Patient with Neurofibromatosis Type 1
40 Case #40:New Diagnosis of Multiple Endocrine Neoplasia Type 2A in a Patient with Bilateral Pheochromocytomas
41 Case #41:Pheochromocytoma in a Patient with von Hippel Lindau Disease
42 Case #42:Bilateral Pheochromocytoma in a Patient with MYC-associated Protein X (MAX) Genetic Predisposition
43 Case #43: The Cystic Pheochromocytoma
44 Case #44: Skull Base and Neck Paragangliomas—Considerations for the Endocrinologist
45 Case #45: Cardiac Paraganglioma.
46 Case #46: Pheochromocytoma in Multiple Endocrine Neoplasia Type 2B
47 Case #47: Metastatic Paraganglioma—An Approach to Management and the Use Serial Imaging to Assess Rate of Tumor Progression
48 Case #48: Metastatic Pheochromocytoma—Role for 68-Ga DOTATATE PET CT
49 Case #49: Carney Triad (Pentad) and Catecholamine-Secreting Paragangliomas
50 Case #50: Metastatic Paraganglioma—Role For Systemic Chemotherapy
51 Case #51: Cryoablation Therapy for Metastatic Paraganglioma
52 Case #52: Paraganglioma in a patient with cyanotic cardiac disease
53 Case #53: Metastatic Paraganglioma—Role For External Beam Radiation Therapy
 Corticotropin (ACTH)-Dependent Hypercortisolism
54 Case #54:ACTH-Dependent Cushing Syndrome can be frequently misdiagnosed
55 Case #55: ACTH-Dependent Cushing Syndrome—Role for Inferior Petrosal Sinus Sampling
56 Case #56: ACTH-Dependent Cushing Syndrome—When Inferior Petrosal Sinus Sampling is Not Needed
57 Case #57: Severe ACTH-Dependent Cushing Syndrome Due to a Pituitary Adenoma
58 Ectopic Cushing Syndrome Associated with Multiple Endocrine Neoplasia Type 2B
59 Case #59:Ectopic Cushing Syndrome Treated with Cryoablation 
60 Cyclical Ectopic Cushing Syndrome
61 Mild Cushing Syndrome Associated with Ectopic Corticotropin Secretion
62 Bilateral Adrenal Cryoablation in Corticotropin-dependent Cushing Syndrome
63 Case #63: Cushing Syndrome Associated with Ectopic Corticotropin and Corticotropin Releasing Hormone Secreting Pheochromocytoma
64 Case #64: Cushing Syndrome in the Setting of Multiple Endocrine Neoplasia Type 1
 G. Other Adrenal Masses
65 Case #65: Adrenal Myelolipoma—A Computed Tomography Diagnosis
66 Case #66: Adrenal Schwannoma
67 Case #67: Trauma-Related Unilateral Adrenal Hemorrhage
68 Case #68: Bilateral Adrenal Hemorrhage
69 Case #69: Primary Adrenal Teratoma
70 Case #70: The Adrenal Stone
71 Case #71: Simple Adrenal Cyst
72 Case #72: Adrenal Cystic Lymphangioma
73 Case #73: Adrenal Hemangioma
74 Case #74: Adrenal Ganglioneuroma
75 Case #75: 42-Year-Old Woman with a Large Adrenal Mass 
76 Case #76: Primary Adrenal Leiomyosarcoma
77 Case #77: Primary Adrenal Lymphoma
78 Case #78. 39-Year-Old Man with a Large Adrenal Mass 
79 Case # 79: 59-Year-Old Man with Enlarging Bilateral Adrenal Masses 
80 Case # 80:65-Year-Old Man with Primary Adrenal Insufficiency 
81 Case #81. 47-Year-Old Man with Primary Adrenal Insufficiency
82 Case #82: Bilateral Adrenal Myelolipoma—Think of Congenital Adrenal Hyperplasia
83 Case #83: A Unilateral Lipid Poor Adrenal Mass—An Atypical Presentation of Adrenal Histoplasmosis
84 Case #84: Bilateral Macronodular Adrenal Hyperplasia (BMAH) in the Setting of Multiple Endocrine Neoplasia Type 1
85 Case #85: Pseudo-Adrenal Masses
 H.Adrenal and Ovarian Hyperandrogenism
86 A Huge Adrenal Myelolipoma in a Patient with a Suboptimally Controlled Congenital Adrenal Hyperplasia
87 Balancing Glucocorticoid and Androgen Excess in Congenital Adrenal Hyperplasia
88 Case #88: Dehydroepiandrosterone-sulfate (DHEA-S): The “Love it” or “Hate it” Hormone
89 Case #89: Sorting out the Source of Androgen Excess in a Postmenopausal Woman with an Adrenal and an Ovarian Mass.
90 Case #90: Primary Testosterone-Secreting Adrenocortical Carcinoma in a Premenopausal Woman.
91 Case #91: Premenopausal Woman with Testosterone-secreting Ovarian Tumor
92 Case #92: Sorting out the Source of Androgen Excess in a Postmenopausal Woman with an Adrenal Mass.
93 Case #93: Testosterone-Secreting Benign Adrenal Adenoma in a Postmenopausal Woman.
 I. Adrenal Disorders in Pregnancy
94 Malignant Pheochromocytoma in Pregnancy
95 Case #95: Catecholamine-Secreting Paraganglioma in Pregnancy
96 Case #96: The Peripartum Diagnosis of Pheochromocytoma and a Genetic Mystery Solved
97 Case #97. History of Pregnancy in a 41-Year-Old Woman with Undiagnosed Cushing syndrome
98 Pregnancy in a Patient with Primary Adrenal Insufficiency
99 Case #99: Pregnancy in a Patient with 21-Hydroxylase Deficiency
100 Primary Aldosteronism in Pregnancy

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