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Severe paraneoplastic hypoglycemia secondary to a gastrointestinal stromal tumour masquerading as a stroke

We report the case of a 70-year-old previously healthy female who presented acutely to the Accident and Emergency department with left-sided vasomotor symptoms including reduced muscle tone, weakness upon walking and slurred speech. Physical examination confirmed hemiparesis with VIIth nerve palsy a...

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Autores principales: Dimitriadis, G K, Gopalakrishnan, K, Rao, R, Grammatopoulos, D K, Randeva, H S, Weickert, M O, Murthy, N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629400/
https://www.ncbi.nlm.nih.gov/pubmed/26535131
http://dx.doi.org/10.1530/EDM-15-0062
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author Dimitriadis, G K
Gopalakrishnan, K
Rao, R
Grammatopoulos, D K
Randeva, H S
Weickert, M O
Murthy, N
author_facet Dimitriadis, G K
Gopalakrishnan, K
Rao, R
Grammatopoulos, D K
Randeva, H S
Weickert, M O
Murthy, N
author_sort Dimitriadis, G K
collection PubMed
description We report the case of a 70-year-old previously healthy female who presented acutely to the Accident and Emergency department with left-sided vasomotor symptoms including reduced muscle tone, weakness upon walking and slurred speech. Physical examination confirmed hemiparesis with VIIth nerve palsy and profound hepatomegaly. A random glucose was low at 1.7 mmol/l, which upon correction resolved her symptoms. In hindsight, the patient recalled having had similar episodes periodically over the past 3 months to which she did not give much attention. While hospitalized, she continued having episodes of symptomatic hypoglycaemia during most nights, requiring treatment with i.v. dextrose and/or glucagon. Blood tests including insulin and C-peptide were invariably suppressed, in correlation with low glucose. A Synacthen stimulation test was normal (Cort (0′) 390 nmol/l, Cort (30′) 773 nmol/l). A computed tomography scan showed multiple lobulated masses in the abdomen, liver and pelvis. An ultrasound guided biopsy of one of the pelvic masses was performed. Immunohistochemistry supported the diagnosis of a gastrointestinal stromal tumour (GIST) positive for CD34 and CD117. A diagnosis of a non islet cell tumour hypoglycaemia (NICTH) secondary to an IGF2 secreting GIST was confirmed with further biochemical investigations (IGF2=96.5 nmol/l; IGF2:IGF1 ratio 18.9, ULN <10). Treatment with growth hormone resolved the patient's hypoglycaemic symptoms and subsequent targeted therapy with Imatinib was successful in controlling disease progression over an 8-year observation period. LEARNING POINTS: NICTH can be a rare complication of GISTs that may manifest with severe hypoglycaemia and neuroglucopenic symptoms. NICTH can masquerade as other pathologies thus causing diagnostic confusion. Histological confirmation of GIST induced NICTH and exclusion of other conditions causing hypoglycaemia is essential. Mutational analysis of GISTs should be carried out in all cases as it guides treatment decision. Tailored management of hypoglycaemia, in this case using growth hormone and targeted cyto-reductive therapy, minimizes the risk of possible life-threatening complications.
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spelling pubmed-46294002015-11-03 Severe paraneoplastic hypoglycemia secondary to a gastrointestinal stromal tumour masquerading as a stroke Dimitriadis, G K Gopalakrishnan, K Rao, R Grammatopoulos, D K Randeva, H S Weickert, M O Murthy, N Endocrinol Diabetes Metab Case Rep Unique/Unexpected Symptoms or Presentations of a Disease We report the case of a 70-year-old previously healthy female who presented acutely to the Accident and Emergency department with left-sided vasomotor symptoms including reduced muscle tone, weakness upon walking and slurred speech. Physical examination confirmed hemiparesis with VIIth nerve palsy and profound hepatomegaly. A random glucose was low at 1.7 mmol/l, which upon correction resolved her symptoms. In hindsight, the patient recalled having had similar episodes periodically over the past 3 months to which she did not give much attention. While hospitalized, she continued having episodes of symptomatic hypoglycaemia during most nights, requiring treatment with i.v. dextrose and/or glucagon. Blood tests including insulin and C-peptide were invariably suppressed, in correlation with low glucose. A Synacthen stimulation test was normal (Cort (0′) 390 nmol/l, Cort (30′) 773 nmol/l). A computed tomography scan showed multiple lobulated masses in the abdomen, liver and pelvis. An ultrasound guided biopsy of one of the pelvic masses was performed. Immunohistochemistry supported the diagnosis of a gastrointestinal stromal tumour (GIST) positive for CD34 and CD117. A diagnosis of a non islet cell tumour hypoglycaemia (NICTH) secondary to an IGF2 secreting GIST was confirmed with further biochemical investigations (IGF2=96.5 nmol/l; IGF2:IGF1 ratio 18.9, ULN <10). Treatment with growth hormone resolved the patient's hypoglycaemic symptoms and subsequent targeted therapy with Imatinib was successful in controlling disease progression over an 8-year observation period. LEARNING POINTS: NICTH can be a rare complication of GISTs that may manifest with severe hypoglycaemia and neuroglucopenic symptoms. NICTH can masquerade as other pathologies thus causing diagnostic confusion. Histological confirmation of GIST induced NICTH and exclusion of other conditions causing hypoglycaemia is essential. Mutational analysis of GISTs should be carried out in all cases as it guides treatment decision. Tailored management of hypoglycaemia, in this case using growth hormone and targeted cyto-reductive therapy, minimizes the risk of possible life-threatening complications. Bioscientifica Ltd 2015-09-21 2015 /pmc/articles/PMC4629400/ /pubmed/26535131 http://dx.doi.org/10.1530/EDM-15-0062 Text en © 2015 The authors This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.en_GB) .
spellingShingle Unique/Unexpected Symptoms or Presentations of a Disease
Dimitriadis, G K
Gopalakrishnan, K
Rao, R
Grammatopoulos, D K
Randeva, H S
Weickert, M O
Murthy, N
Severe paraneoplastic hypoglycemia secondary to a gastrointestinal stromal tumour masquerading as a stroke
title Severe paraneoplastic hypoglycemia secondary to a gastrointestinal stromal tumour masquerading as a stroke
title_full Severe paraneoplastic hypoglycemia secondary to a gastrointestinal stromal tumour masquerading as a stroke
title_fullStr Severe paraneoplastic hypoglycemia secondary to a gastrointestinal stromal tumour masquerading as a stroke
title_full_unstemmed Severe paraneoplastic hypoglycemia secondary to a gastrointestinal stromal tumour masquerading as a stroke
title_short Severe paraneoplastic hypoglycemia secondary to a gastrointestinal stromal tumour masquerading as a stroke
title_sort severe paraneoplastic hypoglycemia secondary to a gastrointestinal stromal tumour masquerading as a stroke
topic Unique/Unexpected Symptoms or Presentations of a Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629400/
https://www.ncbi.nlm.nih.gov/pubmed/26535131
http://dx.doi.org/10.1530/EDM-15-0062
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