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Erschienen in: Pituitary 1/2008

01.03.2008 | Case Report

Remission of acromegaly following long-term therapy with cabergoline: report of two cases

verfasst von: Johan A. Verhelst, Pascale J. Abrams, Roger Abs

Erschienen in: Pituitary | Ausgabe 1/2008

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Abstract

Dopamine agonists are effective in some patients with acromegaly and in this condition treatment is considered to be chronic. We describe two acromegalic patients who responded adequately to the long-acting dopamine agonist cabergoline, but surprisingly maintained normal GH and IGF-I levels once therapy was discontinued after 42 and 76 months because of possibly related side effects. A 32-year-old woman with mild acromegaly (IGF-I: 423 μg/l, GH after OGTT: 2.5 μg/l, adenoma 4 mm) was treated with cabergoline as primary therapy and reached safe GH levels (2 μg/l or less) and normal IGF-I levels with 3.5 mg cabergoline weekly. After 42 months of therapy the patient experienced a progressive decrease of libido, which she attributed to the intake of cabergoline. After stopping medication, serum levels of GH and IGF-I remained normal during the following 2.5 years. A 53-year-old man with moderate acromegaly (serum IGF-I: 547 μg/l, GH after OGTT: 5.9 μg/l, adenoma 7 mm) preferred cabergoline as primary therapy. Serum GH levels below 2 μg/l and normal levels of IGF-I were obtained with 3.5 mg cabergoline weekly. When the patient experienced severe stomach pains after 76 months of treatment, cabergoline was held responsible and discontinued. Serum GH and IGF-I did not increase again and stayed at the same level during a follow-up of 5.5 years. These two cases demonstrate that acromegalic patients with a good response to cabergoline may occasionally remain in remission after stopping therapy. This phenomenon has previously only been described in patients with a prolactinoma.
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Metadaten
Titel
Remission of acromegaly following long-term therapy with cabergoline: report of two cases
verfasst von
Johan A. Verhelst
Pascale J. Abrams
Roger Abs
Publikationsdatum
01.03.2008
Verlag
Springer US
Erschienen in
Pituitary / Ausgabe 1/2008
Print ISSN: 1386-341X
Elektronische ISSN: 1573-7403
DOI
https://doi.org/10.1007/s11102-007-0041-y

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