Clinical and biochemical characteristics of adrenocorticotropin-secreting macroadenomas.

CONTEXT: Cushing's disease as a result of a pituitary macroadenoma is an uncommon cause of Cushing's syndrome, and reports in the published literature are few and of limited size. OBJECTIVE: Our objective was to establish the clinical and biochemical characteristics of macroadenomas assoc...

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Main Authors: Woo, Y, Isidori, A, Wat, W, Kaltsas, G, Afshar, F, Sabin, I, Jenkins, P, Monson, J, Besser, G, Grossman, AB
格式: Journal article
語言:English
出版: 2005
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author Woo, Y
Isidori, A
Wat, W
Kaltsas, G
Afshar, F
Sabin, I
Jenkins, P
Monson, J
Besser, G
Grossman, AB
author_facet Woo, Y
Isidori, A
Wat, W
Kaltsas, G
Afshar, F
Sabin, I
Jenkins, P
Monson, J
Besser, G
Grossman, AB
author_sort Woo, Y
collection OXFORD
description CONTEXT: Cushing's disease as a result of a pituitary macroadenoma is an uncommon cause of Cushing's syndrome, and reports in the published literature are few and of limited size. OBJECTIVE: Our objective was to establish the clinical and biochemical characteristics of macroadenomas associated with Cushing's disease compared with a large cohort of microadenomas and to assess their response to therapy. DESIGN: We conducted a retrospective case-records study for the years 1964-2001. SETTING: The study occurred at a tertiary referral hospital center. PATIENTS: Patients had Cushing's disease presenting with a pituitary macroadenoma, in comparison with a large group of microadenoma patients. INTERVENTIONS: Interventions included therapy with surgery and radiotherapy. MAIN OUTCOME MEASURES: Outcome measures included basal and dynamically responsive plasma ACTH and cortisol levels and response to treatment. RESULTS: We identified 18 patients with Cushing's disease secondary to a macroadenoma; basal 0900 h plasma ACTH was 135.8 +/- 32.5 and 45.0 +/- 4.3 ng/liter (mean +/- SEM), respectively, in macroadenomas and microadenomas (P = 0.013). Mean 0900 h serum cortisol was significantly increased in the macroadenomas (27.5 +/- 3.0 microg/dl, 759.6 +/- 82.6 nmol/liter, vs. 22.6 +/- 0.6 microg/dl, 624.7 +/- 16.4 nmol/liter) (P = 0.021). Testing with high-dose dexamethasone showed less suppression in the macroadenomas (57.6 +/- 8.7% vs. 74.4 +/- 2.1%; P = 0.02) and an attenuated ACTH response to CRH. For all biochemical variables there was considerable overlap between the two groups. Few patients with macroadenomas were cured by surgery. CONCLUSIONS: Pituitary macroadenomas causing Cushing's disease have biochemical features largely distinct from patients harboring microadenomas but represent one end of a continuum.
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spelling oxford-uuid:34640a25-e338-440b-b0df-0c1a3d691c202022-03-26T13:25:40ZClinical and biochemical characteristics of adrenocorticotropin-secreting macroadenomas.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:34640a25-e338-440b-b0df-0c1a3d691c20EnglishSymplectic Elements at Oxford2005Woo, YIsidori, AWat, WKaltsas, GAfshar, FSabin, IJenkins, PMonson, JBesser, GGrossman, AB CONTEXT: Cushing's disease as a result of a pituitary macroadenoma is an uncommon cause of Cushing's syndrome, and reports in the published literature are few and of limited size. OBJECTIVE: Our objective was to establish the clinical and biochemical characteristics of macroadenomas associated with Cushing's disease compared with a large cohort of microadenomas and to assess their response to therapy. DESIGN: We conducted a retrospective case-records study for the years 1964-2001. SETTING: The study occurred at a tertiary referral hospital center. PATIENTS: Patients had Cushing's disease presenting with a pituitary macroadenoma, in comparison with a large group of microadenoma patients. INTERVENTIONS: Interventions included therapy with surgery and radiotherapy. MAIN OUTCOME MEASURES: Outcome measures included basal and dynamically responsive plasma ACTH and cortisol levels and response to treatment. RESULTS: We identified 18 patients with Cushing's disease secondary to a macroadenoma; basal 0900 h plasma ACTH was 135.8 +/- 32.5 and 45.0 +/- 4.3 ng/liter (mean +/- SEM), respectively, in macroadenomas and microadenomas (P = 0.013). Mean 0900 h serum cortisol was significantly increased in the macroadenomas (27.5 +/- 3.0 microg/dl, 759.6 +/- 82.6 nmol/liter, vs. 22.6 +/- 0.6 microg/dl, 624.7 +/- 16.4 nmol/liter) (P = 0.021). Testing with high-dose dexamethasone showed less suppression in the macroadenomas (57.6 +/- 8.7% vs. 74.4 +/- 2.1%; P = 0.02) and an attenuated ACTH response to CRH. For all biochemical variables there was considerable overlap between the two groups. Few patients with macroadenomas were cured by surgery. CONCLUSIONS: Pituitary macroadenomas causing Cushing's disease have biochemical features largely distinct from patients harboring microadenomas but represent one end of a continuum.
spellingShingle Woo, Y
Isidori, A
Wat, W
Kaltsas, G
Afshar, F
Sabin, I
Jenkins, P
Monson, J
Besser, G
Grossman, AB
Clinical and biochemical characteristics of adrenocorticotropin-secreting macroadenomas.
title Clinical and biochemical characteristics of adrenocorticotropin-secreting macroadenomas.
title_full Clinical and biochemical characteristics of adrenocorticotropin-secreting macroadenomas.
title_fullStr Clinical and biochemical characteristics of adrenocorticotropin-secreting macroadenomas.
title_full_unstemmed Clinical and biochemical characteristics of adrenocorticotropin-secreting macroadenomas.
title_short Clinical and biochemical characteristics of adrenocorticotropin-secreting macroadenomas.
title_sort clinical and biochemical characteristics of adrenocorticotropin secreting macroadenomas
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