Advanced acromegaly: successful disease control for more than 16 years using octreotide LA

A 79-year-old male presented with a 10-year history of intermittent headache, sweating, persistent hand numbness and uncontrolled hypertension. He was receiving Nifedipine and Hydrochorothizide. On examination (O/E), his BP was 180/100 he was acromegalic. His growth hormone (GH) was 10 mIU/L (0.0–0....

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Main Authors: Omayma Elshafie, Nicholas Woodhouse
Format: Article
Language:English
Published: Bioscientifica 2021-01-01
Series:Endocrinology, Diabetes & Metabolism Case Reports
Online Access:https://edm.bioscientifica.com/view/journals/edm/2020/1/EDM20-0102.xml
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spelling doaj-b0ae5c243b4045548b0174196eb35c6c2021-01-09T07:08:00ZengBioscientificaEndocrinology, Diabetes & Metabolism Case Reports2052-05732052-05732021-01-01111410.1530/EDM-20-0102Advanced acromegaly: successful disease control for more than 16 years using octreotide LAOmayma Elshafie0Nicholas Woodhouse1Department of Medicine, Sultan Qaboos University Hospital, Muscat, Sultanate of OmanDepartment of Medicine, Sultan Qaboos University Hospital, Muscat, Sultanate of OmanA 79-year-old male presented with a 10-year history of intermittent headache, sweating, persistent hand numbness and uncontrolled hypertension. He was receiving Nifedipine and Hydrochorothizide. On examination (O/E), his BP was 180/100 he was acromegalic. His growth hormone (GH) was 10 mIU/L (0.0–0.1) and his insulin-like growth factor (IGF-1): 952 μg/L (76–160). An MRI of the pituitary revealed a 3 × 2 cm pituitary macroadenoma. Surgery was refused and the family agreed for a therapeutic trial of octreotide. His GH levels fell immediately. Two weeks later he was switched to long-acting monthly octreotide in September 2003. During his 16-year follow-up, he has remained well and asymptomatic off medications for hypertension. His BP and IGF-1 levels were also normal until octreotide Long acting (LA) octrotide was stopped for 3 months at age 96. During this period the IGF-1 level returned to pretreatment levels 500 ng/L (50–141), GH 24 mIU/L (0.0–0.1), and a small residual tumour 0.5–0.8 cm was seen on the MRI. Octreotide LA was restarted and the IGF-1 and GH levels returned to normal. He continues the same treatment to date age 97 without side effects. We conclude that the successful control of IGF-1, GH levels, hypertension, tumour size and clinical symptoms for more than 16 years occurred using octreotide LA in an elderly advanced acromegalic patient. To the best of our knowledge, this is the first report of the successful use of octreotide LA for more than 16 years.https://edm.bioscientifica.com/view/journals/edm/2020/1/EDM20-0102.xml
collection DOAJ
language English
format Article
sources DOAJ
author Omayma Elshafie
Nicholas Woodhouse
spellingShingle Omayma Elshafie
Nicholas Woodhouse
Advanced acromegaly: successful disease control for more than 16 years using octreotide LA
Endocrinology, Diabetes & Metabolism Case Reports
author_facet Omayma Elshafie
Nicholas Woodhouse
author_sort Omayma Elshafie
title Advanced acromegaly: successful disease control for more than 16 years using octreotide LA
title_short Advanced acromegaly: successful disease control for more than 16 years using octreotide LA
title_full Advanced acromegaly: successful disease control for more than 16 years using octreotide LA
title_fullStr Advanced acromegaly: successful disease control for more than 16 years using octreotide LA
title_full_unstemmed Advanced acromegaly: successful disease control for more than 16 years using octreotide LA
title_sort advanced acromegaly: successful disease control for more than 16 years using octreotide la
publisher Bioscientifica
series Endocrinology, Diabetes & Metabolism Case Reports
issn 2052-0573
2052-0573
publishDate 2021-01-01
description A 79-year-old male presented with a 10-year history of intermittent headache, sweating, persistent hand numbness and uncontrolled hypertension. He was receiving Nifedipine and Hydrochorothizide. On examination (O/E), his BP was 180/100 he was acromegalic. His growth hormone (GH) was 10 mIU/L (0.0–0.1) and his insulin-like growth factor (IGF-1): 952 μg/L (76–160). An MRI of the pituitary revealed a 3 × 2 cm pituitary macroadenoma. Surgery was refused and the family agreed for a therapeutic trial of octreotide. His GH levels fell immediately. Two weeks later he was switched to long-acting monthly octreotide in September 2003. During his 16-year follow-up, he has remained well and asymptomatic off medications for hypertension. His BP and IGF-1 levels were also normal until octreotide Long acting (LA) octrotide was stopped for 3 months at age 96. During this period the IGF-1 level returned to pretreatment levels 500 ng/L (50–141), GH 24 mIU/L (0.0–0.1), and a small residual tumour 0.5–0.8 cm was seen on the MRI. Octreotide LA was restarted and the IGF-1 and GH levels returned to normal. He continues the same treatment to date age 97 without side effects. We conclude that the successful control of IGF-1, GH levels, hypertension, tumour size and clinical symptoms for more than 16 years occurred using octreotide LA in an elderly advanced acromegalic patient. To the best of our knowledge, this is the first report of the successful use of octreotide LA for more than 16 years.
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