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Successful Improvement of Metabolic Disorders, Including Osteopenia, by a Dopamine Agonist in a Male Patient with Macro-Prolactinoma

Patient: Male, 43 Final Diagnosis: Prolactinoma Symptoms: — Medication: — Clinical Procedure: Treatments by a dopamine agonist Specialty: Endocrinology and Metabolic OBJECTIVE: Unknown ethiology BACKGROUND: Bone metabolic disorders in patients with prolactinoma have not been fully characterized. The...

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Autores principales: Takeno, Ayumu, Yamamoto, Masahiro, Okazaki, Kyoko, Yamaguchi, Toru, Toshitsugu, Sugimoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792224/
https://www.ncbi.nlm.nih.gov/pubmed/26971354
http://dx.doi.org/10.12659/AJCR.894712
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author Takeno, Ayumu
Yamamoto, Masahiro
Okazaki, Kyoko
Yamaguchi, Toru
Toshitsugu, Sugimoto
author_facet Takeno, Ayumu
Yamamoto, Masahiro
Okazaki, Kyoko
Yamaguchi, Toru
Toshitsugu, Sugimoto
author_sort Takeno, Ayumu
collection PubMed
description Patient: Male, 43 Final Diagnosis: Prolactinoma Symptoms: — Medication: — Clinical Procedure: Treatments by a dopamine agonist Specialty: Endocrinology and Metabolic OBJECTIVE: Unknown ethiology BACKGROUND: Bone metabolic disorders in patients with prolactinoma have not been fully characterized. The case presented herein illustrates potential causal associations between prolactinoma and osteopenia, with a reversal of the disorder by treatment with a dopamine agonist. CASE REPORT: A 43-year-old male with macro-prolactinoma [PRL 7770 ng/mL] was referred to our hospital. He suffered was overweight [body mass index (BMI) 29.4 kg/m(2)] and had impaired glucose tolerance, hypertriglyceridemia, and osteopenia. The patient was administered cabergoline, a dopamine D2 receptor agonist, and the dose was gradually increased up to 9 mg/week over the period of 1 year. One year later, the patient’s serum PRL levels decreased to within the normal range (19.1 ng/mL), and his pituitary tumor mass decreased to 1/4 of its initial size. His weight, dyslipidemia, and impaired glucose tolerance improved within 1 year. A marked increase in the bone mineral density (BMD) at the second to fourth lumbar spine (from 0.801 g/cm(2) to 0.870 g/cm(2), +8.6%) and at the femoral neck (from 0.785 g/cm(2) to 0.864 g/cm(2), +10.1%) were observed despite the presence of unresolved hypogonadism. CONCLUSIONS: Treatments with dopamine agonists represent a beneficial strategy for patients with prolactinoma accompanied with bone loss, in addition to their established efficacy in shrinkage of the size of pituitary tumors, normalization of PRL levels, and improvement of metabolic disorders.
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spelling pubmed-47922242016-03-29 Successful Improvement of Metabolic Disorders, Including Osteopenia, by a Dopamine Agonist in a Male Patient with Macro-Prolactinoma Takeno, Ayumu Yamamoto, Masahiro Okazaki, Kyoko Yamaguchi, Toru Toshitsugu, Sugimoto Am J Case Rep Articles Patient: Male, 43 Final Diagnosis: Prolactinoma Symptoms: — Medication: — Clinical Procedure: Treatments by a dopamine agonist Specialty: Endocrinology and Metabolic OBJECTIVE: Unknown ethiology BACKGROUND: Bone metabolic disorders in patients with prolactinoma have not been fully characterized. The case presented herein illustrates potential causal associations between prolactinoma and osteopenia, with a reversal of the disorder by treatment with a dopamine agonist. CASE REPORT: A 43-year-old male with macro-prolactinoma [PRL 7770 ng/mL] was referred to our hospital. He suffered was overweight [body mass index (BMI) 29.4 kg/m(2)] and had impaired glucose tolerance, hypertriglyceridemia, and osteopenia. The patient was administered cabergoline, a dopamine D2 receptor agonist, and the dose was gradually increased up to 9 mg/week over the period of 1 year. One year later, the patient’s serum PRL levels decreased to within the normal range (19.1 ng/mL), and his pituitary tumor mass decreased to 1/4 of its initial size. His weight, dyslipidemia, and impaired glucose tolerance improved within 1 year. A marked increase in the bone mineral density (BMD) at the second to fourth lumbar spine (from 0.801 g/cm(2) to 0.870 g/cm(2), +8.6%) and at the femoral neck (from 0.785 g/cm(2) to 0.864 g/cm(2), +10.1%) were observed despite the presence of unresolved hypogonadism. CONCLUSIONS: Treatments with dopamine agonists represent a beneficial strategy for patients with prolactinoma accompanied with bone loss, in addition to their established efficacy in shrinkage of the size of pituitary tumors, normalization of PRL levels, and improvement of metabolic disorders. International Scientific Literature, Inc. 2016-03-13 /pmc/articles/PMC4792224/ /pubmed/26971354 http://dx.doi.org/10.12659/AJCR.894712 Text en © Am J Case Rep, 2016 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License
spellingShingle Articles
Takeno, Ayumu
Yamamoto, Masahiro
Okazaki, Kyoko
Yamaguchi, Toru
Toshitsugu, Sugimoto
Successful Improvement of Metabolic Disorders, Including Osteopenia, by a Dopamine Agonist in a Male Patient with Macro-Prolactinoma
title Successful Improvement of Metabolic Disorders, Including Osteopenia, by a Dopamine Agonist in a Male Patient with Macro-Prolactinoma
title_full Successful Improvement of Metabolic Disorders, Including Osteopenia, by a Dopamine Agonist in a Male Patient with Macro-Prolactinoma
title_fullStr Successful Improvement of Metabolic Disorders, Including Osteopenia, by a Dopamine Agonist in a Male Patient with Macro-Prolactinoma
title_full_unstemmed Successful Improvement of Metabolic Disorders, Including Osteopenia, by a Dopamine Agonist in a Male Patient with Macro-Prolactinoma
title_short Successful Improvement of Metabolic Disorders, Including Osteopenia, by a Dopamine Agonist in a Male Patient with Macro-Prolactinoma
title_sort successful improvement of metabolic disorders, including osteopenia, by a dopamine agonist in a male patient with macro-prolactinoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792224/
https://www.ncbi.nlm.nih.gov/pubmed/26971354
http://dx.doi.org/10.12659/AJCR.894712
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