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Title of Journal: Pituitary

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Abbravation: Pituitary

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Springer US

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DOI

10.1002/bies.950190816

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ISSN

1573-7403

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Differential diagnosis of ACTHdependent hypercort

Authors: Massimiliano Andrioli Francesca Pecori Giraldi Martina De Martin Agnese Cattaneo Chiara Carzaniga Francesco Cavagnini
Publish Date: 2009/03/18
Volume: 12, Issue: 4, Pages: 294-
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Abstract

Differential diagnosis of ACTHdependent Cushing’s syndrome often presents major difficulties Diagnostic troubles are increased by suboptimal specificity of endocrine tests the rarity of ectopic ACTH secretion and the frequent incidental discovery of pituitary adenomas A 43yearold female reported with mild signs and symptoms of hypercortisolism and initial hormonal tests and results of pituitary imaging 7mm adenoma were suggestive for Cushing’s disease However inadequate response to corticotrophinreleasing hormone and failure to suppress after 8 mg dexamethasone pointed towards an ectopic source Total body CT scan visualized only a small nonspecific nodule in the right posterior costophrenic excavation Inferior petrosal sinus sampling revealed an absent centerperiphery ACTH gradient but octreoscan and 18FFDGPETCT failed to detect abnormal tracer accumulation We weighed results of the laboratory with those of imaging and decided to remove the lung nodule Pathology identified a typical ACTHstaining carcinoid and the diagnosis was confirmed by postsurgical hypoadrenalism In conclusion imaging may prove unsatisfactory or even misleading for the etiologial diagnosis of ACTHdependent Cushing’s syndrome and should therefore be interpreted only in context with results of hormonal dynamic testing


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Other Papers In This Journal:

  1. IGF-I assays: current assay methodologies and their limitations
  2. Erratum to: An endoscopic modification of the simultaneous ‘above and below’ approach to large pituitary adenomas
  3. Somatostatin receptor ligands in the treatment of acromegaly
  4. Incidence of Cushing’s syndrome and Cushing’s disease in commercially-insured patients <65 years old in the United States
  5. Primary hypothyroidism presenting as pseudoacromegaly
  6. Sellar meningiomas: an endocrinologic perspective
  7. Low frequency of cardniac arrhythmias and lack of structural heart disease in medically-naïve acromegaly patients: a prospective study at baseline and after 1 year of somatostatin analogs treatment
  8. Pituitary tumor apoplexy in patients with Cushing’s disease: endocrinologic and visual outcomes after transsphenoidal surgery
  9. A comparison of cabergoline and bromocriptine on the risk of valvular heart disease in patients with prolactinomas
  10. Sellar and clival plasmacytomas: case series of 5 patients with systematic review of 65 published cases
  11. Analysis of GNAS mutations in 60 growth hormone secreting pituitary tumors: correlation with clinical and pathological characteristics and surgical outcome based on highly sensitive GH and IGF-I criteria for remission
  12. Sellar plasmacytomas: a concise review
  13. Increased clinical symptoms of acromegalic arthropathy in patients with long-term disease control: a prospective follow-up study
  14. Two cases of Kallmann syndrome associated with empty sella
  15. Multiple head and neck tumors following treatment for craniopharyngioma
  16. Modulation of VEGF/Flk-1 receptor expression in the rat pituitary GH3 cell line by growth factors
  17. Acromegalic gigantism, physicians and body snatching. Past or present?
  18. Effectiveness of self- or partner-administration of an extended-release aqueous-gel formulation of lanreotide in lanreotide-naïve patients with acromegaly
  19. Adipsic diabetes insipidus in adult patients
  20. Pituitary gland and β-catenin signaling: from ontogeny to oncogenesis
  21. A novel variation in the AVP gene resulting in familial neurohypophyseal diabetes insipidus in a large Italian kindred

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