By Steven Jon Russell, Karen Klahr Miller (auth.), Terry F. Davies (eds.)

ISBN-10: 1588298159

ISBN-13: 9781588298157

ISBN-10: 1603271031

ISBN-13: 9781603271035

Written situations offer a considerate evaluate of recent administration and contemplation of the literature, even more so than even a case presentation with out the sufferer. for that reason, lately the written or ready case has turn into the suitable discussion board for demonstrating the best way to deal with a clinical challenge to the best good thing about the sufferer. In A Case-Based consultant to medical Endocrinology, amazing clinicians offer stimulating guide and insights right into a good selection of endocrine topics, instructing readers sleek administration of the stipulations defined and delivering designated access into the literature. Importantly, a number of the vital parts within the present curriculum for scientific endocrine education as advised via the organization of application administrators in medical Endocrinology, Diabetes and Metabolism are lined during this textual content. to enhance studying and retention of data, every one writer has additionally supplied a number of selection questions following the case reviews. scholars, citizens, fellows, and practitioners will locate those examples to be an effective approach to assessment their figuring out and raise their abilities and talents in sufferer research and administration.

In all, A Case-Based consultant to scientific Endocrinology bargains a finished quantity of concise case-studies that would end up to be of important value to all clinicians practising during this box.

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A retrospective analysis of pituitary apoplexy. Neurosurgery 1993;33(4):602–608; discussion 608–609. 2. Rolih CA, Ober KP. Pituitary apoplexy. Endocrinol Metab Clin North Am 1993;22(2):291–302. 3. Maccagnan P, Macedo CL, Kayath MJ, Nogueira RG, Abucham J. Conservative management of pituitary apoplexy: a prospective study. J Clin Endocrinol Metab 1995;80(7):2190–2197. 4. Sibal L, Ball SG, Connolly V, et al. Pituitary apoplexy: a review of clinical presentation, management and outcome in 45 cases.

Eur J Endocrinol 1996;134: 454–456. 6. Colao A, Di Sarno A, Sarnacchiaro F, et al. Prolactinomas resistant to standard dopamine agonists respond to chronic cabergoline treatment. J Clin Endocrinol Metab 1997;82:876–883. 7. Di Sarno A, Landi ML, Cappabianca P, et al. Resistance to cabergoline as compared with bromocriptine in hyperprolactinemia: prevalence, clinical definition, and therapeutic strategy. J Clin Endocrinol Metab 2001;86:5256–5261. 8. Colao A, Di Sarno A, Cappabianca P, Di Somma C, Pivonello R, Lombardi G.

There is no clear preference for one tumor type Answer: D. Although individual case series have reported a predominance of certain tumor types, the findings are not consistent. When taken together, the case series reports do not reveal a clear predominance for one tumor type, but the three tumor types listed are significantly more common than corticotroph adenomas and TSH secreting adenomas. Chapter 2 When and How to Stop Cabergoline Treatment in Microprolactinomas Annamaria Colao Prolactinomas are the most frequent pituitary tumors with an estimated prevalence in the adult population of 100 per million population [1].

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A Case-Based Guide to Clinical Endocrinology by Steven Jon Russell, Karen Klahr Miller (auth.), Terry F. Davies (eds.)


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