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Glucagonoma-associated dilated cardiomyopathy refractory to somatostatin analogue therapy

A 67-year-old woman presented with a generalised rash associated with weight loss and resting tachycardia. She had a recent diagnosis of diabetes mellitus. Biochemical evaluation revealed elevated levels of circulating glucagon and chromogranin B. Cross-sectional imaging demonstrated a pancreatic le...

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Autores principales: Barabas, Michal, Huang-Doran, Isabel, Pitfield, Debbie, Philips, Hazel, Goonewardene, Manoj, Casey, Ruth T, Challis, Benjamin G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432982/
https://www.ncbi.nlm.nih.gov/pubmed/30836327
http://dx.doi.org/10.1530/EDM-18-0157
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author Barabas, Michal
Huang-Doran, Isabel
Pitfield, Debbie
Philips, Hazel
Goonewardene, Manoj
Casey, Ruth T
Challis, Benjamin G
author_facet Barabas, Michal
Huang-Doran, Isabel
Pitfield, Debbie
Philips, Hazel
Goonewardene, Manoj
Casey, Ruth T
Challis, Benjamin G
author_sort Barabas, Michal
collection PubMed
description A 67-year-old woman presented with a generalised rash associated with weight loss and resting tachycardia. She had a recent diagnosis of diabetes mellitus. Biochemical evaluation revealed elevated levels of circulating glucagon and chromogranin B. Cross-sectional imaging demonstrated a pancreatic lesion and liver metastases, which were octreotide-avid. Biopsy of the liver lesion confirmed a diagnosis of well-differentiated grade 2 pancreatic neuroendocrine tumour, consistent with metastatic glucagonoma. Serial echocardiography commenced 4 years before this diagnosis demonstrated a progressive left ventricular dilatation and dysfunction in the absence of ischaemia, suggestive of glucagonoma-associated dilated cardiomyopathy. Given the severity of the cardiac impairment, surgical management was considered inappropriate and somatostatin analogue therapy was initiated, affecting clinical and biochemical improvement. Serial cross-sectional imaging demonstrated stable disease 2 years after diagnosis. Left ventricular dysfunction persisted, however, despite somatostatin analogue therapy and optimal medical management of cardiac failure. In contrast to previous reports, the case we describe demonstrates that chronic hyperglucagonaemia may lead to irreversible left ventricular compromise. Management of glucagonoma therefore requires careful and serial evaluation of cardiac status. LEARNING POINTS: In rare cases, glucagonoma may present with cardiac failure as the dominant feature. Significant cardiac impairment may occur in the absence of other features of glucagonoma syndrome due to subclinical chronic hyperglucagonaemia. A diagnosis of glucagonoma should be considered in patients with non-ischaemic cardiomyopathy, particularly those with other features of glucagonoma syndrome. Cardiac impairment due to glucagonoma may not respond to somatostatin analogue therapy, even in the context of biochemical improvement. All patients with a new diagnosis of glucagonoma should be assessed clinically for evidence of cardiac failure and, if present, a baseline transthoracic echocardiogram should be performed. In the presence of cardiac impairment these patients should be managed by an experienced cardiologist.
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spelling pubmed-64329822019-03-27 Glucagonoma-associated dilated cardiomyopathy refractory to somatostatin analogue therapy Barabas, Michal Huang-Doran, Isabel Pitfield, Debbie Philips, Hazel Goonewardene, Manoj Casey, Ruth T Challis, Benjamin G Endocrinol Diabetes Metab Case Rep Unique/Unexpected Symptoms or Presentations of a Disease A 67-year-old woman presented with a generalised rash associated with weight loss and resting tachycardia. She had a recent diagnosis of diabetes mellitus. Biochemical evaluation revealed elevated levels of circulating glucagon and chromogranin B. Cross-sectional imaging demonstrated a pancreatic lesion and liver metastases, which were octreotide-avid. Biopsy of the liver lesion confirmed a diagnosis of well-differentiated grade 2 pancreatic neuroendocrine tumour, consistent with metastatic glucagonoma. Serial echocardiography commenced 4 years before this diagnosis demonstrated a progressive left ventricular dilatation and dysfunction in the absence of ischaemia, suggestive of glucagonoma-associated dilated cardiomyopathy. Given the severity of the cardiac impairment, surgical management was considered inappropriate and somatostatin analogue therapy was initiated, affecting clinical and biochemical improvement. Serial cross-sectional imaging demonstrated stable disease 2 years after diagnosis. Left ventricular dysfunction persisted, however, despite somatostatin analogue therapy and optimal medical management of cardiac failure. In contrast to previous reports, the case we describe demonstrates that chronic hyperglucagonaemia may lead to irreversible left ventricular compromise. Management of glucagonoma therefore requires careful and serial evaluation of cardiac status. LEARNING POINTS: In rare cases, glucagonoma may present with cardiac failure as the dominant feature. Significant cardiac impairment may occur in the absence of other features of glucagonoma syndrome due to subclinical chronic hyperglucagonaemia. A diagnosis of glucagonoma should be considered in patients with non-ischaemic cardiomyopathy, particularly those with other features of glucagonoma syndrome. Cardiac impairment due to glucagonoma may not respond to somatostatin analogue therapy, even in the context of biochemical improvement. All patients with a new diagnosis of glucagonoma should be assessed clinically for evidence of cardiac failure and, if present, a baseline transthoracic echocardiogram should be performed. In the presence of cardiac impairment these patients should be managed by an experienced cardiologist. Bioscientifica Ltd 2019-03-05 /pmc/articles/PMC6432982/ /pubmed/30836327 http://dx.doi.org/10.1530/EDM-18-0157 Text en © 2019 The authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. (http://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Unique/Unexpected Symptoms or Presentations of a Disease
Barabas, Michal
Huang-Doran, Isabel
Pitfield, Debbie
Philips, Hazel
Goonewardene, Manoj
Casey, Ruth T
Challis, Benjamin G
Glucagonoma-associated dilated cardiomyopathy refractory to somatostatin analogue therapy
title Glucagonoma-associated dilated cardiomyopathy refractory to somatostatin analogue therapy
title_full Glucagonoma-associated dilated cardiomyopathy refractory to somatostatin analogue therapy
title_fullStr Glucagonoma-associated dilated cardiomyopathy refractory to somatostatin analogue therapy
title_full_unstemmed Glucagonoma-associated dilated cardiomyopathy refractory to somatostatin analogue therapy
title_short Glucagonoma-associated dilated cardiomyopathy refractory to somatostatin analogue therapy
title_sort glucagonoma-associated dilated cardiomyopathy refractory to somatostatin analogue therapy
topic Unique/Unexpected Symptoms or Presentations of a Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432982/
https://www.ncbi.nlm.nih.gov/pubmed/30836327
http://dx.doi.org/10.1530/EDM-18-0157
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