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Cabergoline in severe ectopic or occult Cushing's syndrome.
Ilie, Mirela Diana; Raverot, Véronique; Tronc, François; Vasiljevic, Alexandre; Borson-Chazot, Françoise; Raverot, Gérald.
Afiliação
  • Ilie MD; Endocrinology Department, 'Groupement Hospitalier Est' Hospices Civils de Lyon, Lyon, France.
  • Raverot V; Lyon 1 University, Lyon, France.
  • Tronc F; Biochemistry Laboratory Department, 'Groupement Hospitalier Est' Hospices Civils de Lyon, Lyon, France.
  • Vasiljevic A; Lyon 1 University, Lyon, France.
  • Borson-Chazot F; Thoracic Surgery Department, 'Groupement Hospitalier Est' Hospices Civils de Lyon, Lyon, France.
  • Raverot G; Lyon 1 University, Lyon, France.
Eur J Endocrinol ; 181(1): K1-K9, 2019 Jul 01.
Article em En | MEDLINE | ID: mdl-31048558
ABSTRACT
CONTEXT Cabergoline has been shown to have some effect in the treatment of moderate Cushing's disease, but its effectiveness in Cushing's syndrome of ectopic or occult origin remains to be investigated. CASE SERIES In this case series, cabergoline was used in combination with steroidogenesis inhibitors in nine patients with severe Cushing's syndrome of ectopic or occult origin. Cabergoline's effectiveness enabled rapid withdrawal of the steroidogenesis inhibitors and long-term control of the hypercortisolism in three of the cases. REVIEW OF THE LITERATURE In the literature, we found only 11 cases of ectopic or occult Cushing's syndrome treated with dopamine receptor agonists, alone or in combination. Yet of these 11 cases, 10 responded.

CONCLUSIONS:

Although limited, the existing experience highlights the potential value of cabergoline in the treatment of ectopic or occult Cushing's syndrome.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Agonistas de Dopamina / Síndrome de Cushing / Cabergolina Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Agonistas de Dopamina / Síndrome de Cushing / Cabergolina Idioma: En Ano de publicação: 2019 Tipo de documento: Article