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Síndroma de Cushing ACTH-dependente: estudo retrospectivo

dc.contributor.authorPaiva, I
dc.contributor.authorRibeiro, C
dc.contributor.authorGomes, L
dc.contributor.authorBaptista, C
dc.contributor.authorGomes, F
dc.contributor.authorRito, M
dc.contributor.authorRebelo, O
dc.contributor.authorMarnoto, D
dc.contributor.authorMoura, C
dc.contributor.authorLeitão, F
dc.contributor.authorCarvalheiro, M
dc.date.accessioned2008-11-28T14:55:28Z
dc.date.available2008-11-28T14:55:28Z
dc.date.issued2004
dc.description.abstractAIM: To evaluate the characteristics and outcomes of the patients diagnosed as ACTH-dependent Cushing syndrome, registered in the department. MATERIAL AND METHODS: We reviewed the files of forty-three patients followed from 1974 to 2002. RESULTS: A progressive rise in the number of patients diagnosed was found, being 80% females. Clinical suspicion was based mostly on the typical fat distribution; hirsutism and amenorrhoea were important in women. The more reliable diagnostic tests were: 11 pm cortisol, day curve of ACTH and cortisol, and dexamethasone suppression tests. The ACTH response to CRH during inferior petrosal sinus sampling permitted the diagnosis of ectopic source. In thirty-seven patients a pituitary adenoma was diagnosed. The three patients diagnosed before 1985 went for bilateral adrenalectomy (Nelson's syndrome in two); the others were submitted to transsphenoidal pituitary adenomectomy, obtaining remission in twenty six at the first operation and in two others at the second. Three patients had a recidive. Of the six patients with persistent disease (all treated with metyrapone or ketoconazole), three were submitted to radiotherapy, two to bilateral adrenalectomy, and one was waiting for surgery. Four patients had a bronchial carcinoid, successfully removed in three. One patient was lost to follow-up and another was still being evaluated. CONCLUSIONS: We found a positive evolution in the capacity to diagnose and treat these patients. Neurosurgical ability to achieve remission was 80% in the operated cases. More effective technical methods and drugs, as well as a multidisciplinary and dedicated medical team, lead to long lasting remissions in most of the patients.en
dc.identifier.citationActa Med Port. 2004 Sep-Oct;17(5):367-74en
dc.identifier.urihttp://hdl.handle.net/10400.4/234
dc.language.isoporen
dc.publisherCentro Editor Livreiro da Ordem dos Médicosen
dc.subjectSíndrome de Cushingen
dc.titleSíndroma de Cushing ACTH-dependente: estudo retrospectivoen
dc.title.alternativeACTH-dependent Cushing's syndrome: a revision of 43 casesen
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccess
rcaap.typearticleen

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