Cushing's Syndrome
Pathophysiology, Diagnosis and Treatment
(Sprache: Englisch)
CushingŽs syndrome is a relatively rare clinical disorder that is associated with many co-morbidities such as systemic hypertension, diabetes, osteoporosis, impaired immune function and growth impairment in children, all of which severely reduce quality of...
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CushingŽs syndrome is a relatively rare clinical disorder that is associated with many co-morbidities such as systemic hypertension, diabetes, osteoporosis, impaired immune function and growth impairment in children, all of which severely reduce quality of life and life expectancy. Cushing's Syndrome: Pathophysiology, Diagnosis and Treatment reviews the difficulties in distinguishing Cushing's syndrome from these and other common conditions, such as central obesity, menstrual irregularity and depression. It also provides state-of-the-art information on various strategies to establish the diagnosis of Cushing's syndrome and the differential diagnosis among its diverse etiologies, as well as therapeutic approaches. Additionally, a range of conditions that represent challenges for the diagnosis and treatment--such as renal failure, pediatric age, cyclic hypercortisolism, and pregnancy--are covered in detail. A valuable resource not only for endocrinologists but also internal medicine physicians, gynecologists, pediatricians, , pituitary surgeons and urologists, Cushing's Syndrome: Pathophysiology, Diagnosis and Treatment provides insights by experts that will help all physicians dealing with CushingŽs syndrome to expand their knowledge about the condition and provide targeted, comprehensive care.
Klappentext zu „Cushing's Syndrome “
Cushing´s syndrome is a relatively rare clinical disorder that is associated with many co-morbidities such as systemic hypertension, diabetes, osteoporosis, impaired immune function and growth impairment in children, all of which severely reduce quality of life and life expectancy. Cushing's Syndrome: Pathophysiology, Diagnosis and Treatment reviews the difficulties in distinguishing Cushing's syndrome from these and other common conditions, such as central obesity, menstrual irregularity and depression. It also provides state-of-the-art information on various strategies to establish the diagnosis of Cushing's syndrome and the differential diagnosis among its diverse etiologies, as well as therapeutic approaches. Additionally, a range of conditions that represent challenges for the diagnosis and treatment--such as renal failure, pediatric age, cyclic hypercortisolism, and pregnancy--are covered in detail. A valuable resource not only for endocrinologists but also internal medicine physicians, gynecologists, pediatricians, , pituitary surgeons and urologists, Cushing's Syndrome: Pathophysiology, Diagnosis and Treatment provides insights by experts that will help all physicians dealing with Cushing´s syndrome to expand their knowledge about the condition and provide targeted, comprehensive care.
Inhaltsverzeichnis zu „Cushing's Syndrome “
Physiology and Pathophysiology of the HPA axis.- Etiologies of Cushing´s syndrome.- Pathogenesis of corticotropic tumors.- Pathogenesis of adrenocortical tumors.- Clinical features of Cushing´s syndrome.- Laboratorial diagnosis of Cushing´s Syndrome: Differential diagnosis with pseudo-Cushing´s conditions as obesity, alcoholism and depression.- Laboratorial diagnosis of Cushing´s syndrome: Differential diagnosis among the different causes of ACTH-dependent and ACTH-independent Cushing´s syndrome.- Imaging for the differential diagnosis of Cushing´s syndrome: MRI, CT and isotopic scanning.- Inferior petrosal sampling for the differential diagnosis of ACTH dependent Cushing´s syndrome.- ACTH-dependent Cushing syndrome: Treatment of Cushing´s disease.- Treatment of Cushings Syndrome: Surgical Treatment.- Adrenal-Directed Treatment Options for Cushing's Disease.- Radiation Therapy and Stereotactic Radiosurgery for Cushing's Disease.- Medical Management of Cushing's syndrome.- ACTH-dependent Cushing syndrome: Clinical and diagnostic aspects, and treatment approaches for ectopic Cushing´s syndrome.- Revisiting the Nelson's syndrome: Corticotroph Tumor Progression after bilateral adrenalectomy in Cushing's disease.- ACTH-independent Cushing´s syndrome: Adrenocortical tumors.- ACTH-independent Cushing´s syndrome: Bilateral macronodular hyperplasia.- ACTH-independent Cushing´s syndrome: primary pigmented nodular adrenal disease in the context of Carney´s complex.- Glucocorticoid Resistance.- Post-operative replacement and assessment of HPA axis recovery in Cushing's syndrome.- Special aspects of Cushing´s syndrome: Pregnancy.- Special aspects of Cushing´s syndrome: Childhood.- Special aspects of Cushing´s syndrome: Cyclic Cushing´s syndrome.
Bibliographische Angaben
- 2012, Repr. d. Ausg. v. 2011, XII, 304 Seiten, Maße: 19,3 x 26 cm, Kartoniert (TB), Englisch
- Herausgegeben: Marcello D. Bronstein
- Verlag: Springer, Berlin
- ISBN-10: 161779709X
- ISBN-13: 9781617797095
Sprache:
Englisch
Pressezitat
From the reviews:"This book contains 23 chapters written by 56 carefully selected experts from three continents. There are special chapters on physiology and pathophysiology of hypothalamic-pituitary-adrenal system as well as on the etiology of Cushing's syndrome. ... Several chapters deal in detail with surgical management, adrenal directed treatment, radiation therapy and medical management. ... this book gives outstanding knowledge and is enriching the contemporaneous status of art on Cushing's syndrome." (Endocrine Regulations, January, 2012)
"Part of the Contemporary Endocrinology series, a very comprehensive treatise on this difficult to diagnose and treat to disease. Written by multidisciplinary scientists from several countries, it reviews in 23 chapters the physiology and pathophysiology of the HPA axis, the etiology and clinical features of Cushing's syndrome (CS), diagnostic methods and problems, the various methods of treatment and differential diagnosis including ACTH independent CS. ... Clearly written and highly illustrated ... . Recommended." (Pediatric Endocrinology Reviews (PER), Vol. 9 (2), December, 2011)
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