Internal Medicine
Online ISSN : 1349-7235
Print ISSN : 0918-2918
ISSN-L : 0918-2918

This article has now been updated. Please use the final version.

Successful Therapy Using Pasireotide Long-acting Release for Cushing's Disease Merged with Biochemical Acromegaly
Kensaku FukunagaHitomi ImachiSeisuke SatoToshihiro KobayashiYuki YoshiokaTakanobu SahekiNatsuki BanKurumi UrushiharaJingya LyuTao DongRyou IshikawaKyuichi KadotaReiji HabaNaoko InoshitaKoji Murao
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JOURNAL OPEN ACCESS Advance online publication

Article ID: 4663-20

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Abstract

It is quite rare that Cushing's disease shows acromegaly, and no pharmacotherapy has yet been discussed. A 21-year-old woman was diagnosed with Cushing's disease and underwent trans-sphenoidal surgery. Five years later, she was diagnosed with recurrent Cushing's disease and biochemical acromegaly because of elevated levels of serum growth hormone (GH), plasma insulin-like growth factor-1, plasma adrenocorticotropic hormone (ACTH), and the 24-h urinary excretion of free cortisol. After treatment initiation with pasireotide-long-acting release (LAR), both the ACTH and GH declined. Our case is the first to show the efficacy of pasireotide-LAR in controlling both Cushing's disease and acromegaly.

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© 2021 by The Japanese Society of Internal Medicine
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