How could hypoglycemia-inducing glycogen storage disease lead to hyperglycemia-induced mucormycosis?

ABSTRACT Mucormycosis is an increasingly frequent, difficult to diagnose, difficult to treat, often fatal infection, especially in patients with hyperglycemia from uncontrolled diabetes. Type I (von Gierke) glycogen storage disease is due to inherited deficiency of enzymes in glycogen metabolism, which causes hypoglycemia. This report is the case of a patient with von Gierke disease and a missed diagnosis of pulmonary mucormycosis. This report illustrates the importance of having a high index of suspicion for mucormycosis in the appropriate clinical context.

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Main Authors: Nichols,Larry, Rios,Diana Alejandra
Format: Digital revista
Language:English
Published: Hospital Universitário da Universidade de São Paulo 2020
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2236-19602020000100305
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spelling oai:scielo:S2236-196020200001003052020-10-19How could hypoglycemia-inducing glycogen storage disease lead to hyperglycemia-induced mucormycosis?Nichols,LarryRios,Diana Alejandra Mucor Lung Diseases, Fungal Glycogen Storage Disease Type I Autopsy ABSTRACT Mucormycosis is an increasingly frequent, difficult to diagnose, difficult to treat, often fatal infection, especially in patients with hyperglycemia from uncontrolled diabetes. Type I (von Gierke) glycogen storage disease is due to inherited deficiency of enzymes in glycogen metabolism, which causes hypoglycemia. This report is the case of a patient with von Gierke disease and a missed diagnosis of pulmonary mucormycosis. This report illustrates the importance of having a high index of suspicion for mucormycosis in the appropriate clinical context.info:eu-repo/semantics/openAccessHospital Universitário da Universidade de São PauloAutopsy and Case Reports v.10 n.1 20202020-01-01info:eu-repo/semantics/reporttext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S2236-19602020000100305en10.4322/acr.2020.149
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country Brasil
countrycode BR
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databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Nichols,Larry
Rios,Diana Alejandra
spellingShingle Nichols,Larry
Rios,Diana Alejandra
How could hypoglycemia-inducing glycogen storage disease lead to hyperglycemia-induced mucormycosis?
author_facet Nichols,Larry
Rios,Diana Alejandra
author_sort Nichols,Larry
title How could hypoglycemia-inducing glycogen storage disease lead to hyperglycemia-induced mucormycosis?
title_short How could hypoglycemia-inducing glycogen storage disease lead to hyperglycemia-induced mucormycosis?
title_full How could hypoglycemia-inducing glycogen storage disease lead to hyperglycemia-induced mucormycosis?
title_fullStr How could hypoglycemia-inducing glycogen storage disease lead to hyperglycemia-induced mucormycosis?
title_full_unstemmed How could hypoglycemia-inducing glycogen storage disease lead to hyperglycemia-induced mucormycosis?
title_sort how could hypoglycemia-inducing glycogen storage disease lead to hyperglycemia-induced mucormycosis?
description ABSTRACT Mucormycosis is an increasingly frequent, difficult to diagnose, difficult to treat, often fatal infection, especially in patients with hyperglycemia from uncontrolled diabetes. Type I (von Gierke) glycogen storage disease is due to inherited deficiency of enzymes in glycogen metabolism, which causes hypoglycemia. This report is the case of a patient with von Gierke disease and a missed diagnosis of pulmonary mucormycosis. This report illustrates the importance of having a high index of suspicion for mucormycosis in the appropriate clinical context.
publisher Hospital Universitário da Universidade de São Paulo
publishDate 2020
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2236-19602020000100305
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