By Edward R. Laws, Shereen Ezzat, Sylvia L. Asa, Visit Amazon's Linda M. Rio Page, search results, Learn about Author Central, Linda M. Rio, , Lorin Michel, Robert Knutzen
Do you need to be modern at the most up-to-date techniques of analysis and therapy of sufferers struggling with issues of the pituitary gland?
Are you searching for knowledgeable consultant to the simplest medical management?
If so, this can be the e-book for you, delivering a whole research of pituitary disease administration from acromegaly to Addison’s illness; from Cushing’s illness to hypopituitarism; from hormone issues to hormone replacement
Well-illustrated all through and with contributions from best experts in pituitary disorder, inside of you’ll locate finished and professional insurance, including:
- Diagnosing pituitary disease
- Management techniques for every disorder
- Complications which could occur
- Psychological and psychosocial results of pituitary disease
- What results you and your sufferers can count on over the lengthy term
- Current examine and medical trials concerning pituitary disease
Pituitary issues: analysis and Management is the proper medical instrument for physicians and well-being care companies from many comparable disciplines, and a necessary significant other for the very best quality administration of pituitary patients.
Chapter 1 The Endocrine procedure (pages 1–12): Sylvia L. Asa and Shereen Ezzat
Chapter 2 symptoms of Pituitary ailment (pages 13–20): Eva Fernandez?Rodriguez, Ignacio Bernabeu, Felipe F. Casanueva, Eva N. Kassi, Gregory A. Kaltsas, George P. Chrousos and Valerie Golden
Chapter three Acromegaly (pages 21–31): Shereen Ezzat
Chapter four Secondary Adrenal Insufficiency (pages 32–46): Tobias Else and Richard J. Auchus
Chapter five grownup progress Hormone Deficiency (pages 47–54): T. Brooks Vaughan, Kristen Owen Riley and Lewis S. Blevins
Chapter 6 Pituitary Carcinoma (pages 55–58): Sylvia L. Asa
Chapter 7 Craniopharyngioma (pages 59–66): Jessica ok. Devin
Chapter eight Cushing's Syndrome (pages 67–76): Lewis S. Blevins
Chapter nine Empty Sella Syndrome (pages 77–86): Michael C. Oh and Manish okay. Aghi
Chapter 10 Familial Pituitary Adenomas (pages 87–110): Laura C. Hernandez?Ramirez and Marta Korbonits
Chapter eleven Follicle Stimulating Hormone and Luteinizing Hormone Secreting Tumors (pages 111–119): Bahram Khazai, Ronald S. Swerdloff and Christina Wang
Chapter 12 Hypopituitarism (pages 120–129): Klara J. Rosenquist and Ursula B. Kaiser
Chapter thirteen Clinically Nonfunctioning Pituitary Adenomas (pages 130–137): Brandon A. Miller, Adriana G. Ioachimescu and Nelson M. Oyesiku
Chapter 14 Prolactinoma (pages 138–145): Luis G. Sobrinho
Chapter 15 Rathke's Cleft Cysts (pages 146–152): Seunggu J. Han, Arman Jahangiri and Manish okay. Aghi
Chapter sixteen Thyroid Hormone Deficiency (pages 153–158): Whitney W. Woodmansee
Chapter 17 Thyroid Stimulating Hormone Secreting Tumor (pages 159–166): Andrea Lania, Luca Persani and Paolo Beck?Peccoz
Chapter 18 Pituitary issues – particular matters for girls (pages 167–178): Maria Fleseriu, Christine G. Yedinak, Jessica Brzana and Shirley McCartney
Chapter 19 Hypogonadism and Male Sexual functionality (pages 179–192): Prasanth N. Surampudi, Christina Wang and Ronald S. Swerdloff
Chapter 20 Pituitary problems particular to young ones (pages 193–203): Kathryn Pade and Mitchell E. Geffner
Chapter 21 actual exam (pages 205–212): Laurence Katznelson
Chapter 22 Pituitary Endocrine functionality checking out (pages 213–224): Shereen Ezzat
Chapter 23 clinical administration of Pituitary Adenomas (pages 225–242): Paolo Cappabianca, Daniel M. Prevedello, Michelangelo de Angelis, Andressa Bornschein, Leo F. S. Ditzel Filho, Domenico Solari, Ricardo L. Carrau, Felice Esposito, Danielle de Lara, Luigi M. Cavallo and Annamaria Colao
Chapter 24 Surgical administration of Pituitary issues (pages 243–254): Gautam U. Mehta, John A. Jane, Ian F. Dunn, Tong Yang, Theodore H. Schwartz, Huy T. Duong and Daniel F. Kelly
Chapter 25 Stereotactic Radiosurgery for Pituitary Adenomas (pages 255–264): Brian J. Williams, Stephen J. Monteith and Jason P. Sheehan
Chapter 26 Hormone substitute treatment (pages 265–276): Joseph A. M. J. L. Janssen, Aart Jan van der Lely, Alan D. Rogol and Adriana G. Ioachimescu
Chapter 27 problems of Pituitary sickness (pages 277–290): Ludovica F. S. Grasso, Alessia Cozzolino, Annamaria Colao, Krystallenia I. Alexandraki, Gregory A. Kaltsas, George P. Chrousos, Marco Faustini?Fustini, Giorgio Frank, Paul B. Rizzoli, Andrea L. Utz and Sashank Prasad
Chapter 28 common mental and Psychosocial results of Pituitary problems (pages 291–299): Valerie Golden
Chapter 29 dwelling with Pituitary ailment (pages 301–310): Jessica okay. Devin
Chapter 30 study and scientific Trials (pages 311–322): Brittany P. Sumerel and Anthony P. Heaney
Chapter 31 basics of Pituitary Pathology (pages 323–332): Sylvia L. Asa
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Additional info for Pituitary Disorders: Diagnosis and Management
There is also general agreement that survival among acromegalic patients is reduced by an average of 10 years. A multicenter retrospective cohort study of 1362 patients from the United Kingdom also revealed that mortality rate due to colon cancer was higher than expected. 5 ng/mL was comparable to the general population. These data provide the framework for more rational objective measures to validate treatment outcomes. therapy may be considered in the absence of optic chiasma compression, particularly in patients with high surgical risk and/or those whose tumors are not amenable to complete resection.
Delayed diagnosis of adrenal insufficiency is common: a crosssectional study in 216 patients. Am J Med Sci 2010; 339: 525–531. 28. Raison CL, Miller AH. When not enough is too much: the role of insufficient glucocorticoid signaling in the pathophysiology of stress-related disorders. Am J Psychiatry 2003; 160: 1554–1565. 29. Wainwright SR, Lieblich SE, Galea LA. Hypogo nadism predisposes males to the development of behavioural and neuroplastic depressive phenotypes. Psychoneuroendocrinology 2011; 36: 1327–1341.
Symptoms and signs of secondary adrenal insufficiency Constitutional Clinical Presentation The clinical presentation of secondary adrenal insufficiency is highly variable and dependent on the progression of the underlying disease process and coexistence of additional pituitary deficits. Secondary adrenal insufficiency often presents in a more insidious manner than primary adrenal insufficiency, due to both preserved mineralocorticoid production and in most cases partial deficiency.