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Autops. Case Rep ; 10(1): e2020149, Jan.-Mar. 2020. ilus
Article in English | LILACS | ID: biblio-1053543

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.


Subject(s)
Humans , Female , Adult , Glycogen Storage Disease Type I/pathology , Lung Diseases, Fungal/pathology , Mucormycosis/pathology , Autopsy , Fatal Outcome , Diagnosis, Differential
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