Glycogenic Hepatopathy: A Rare Hepatic Complication of Poorly Controlled Type 1 DM

Glycogen hepatopathy (GH) is a rare complication of type 1 diabetes mellitus that leads to an abnormal accumulation of glycogen in the hepatocytes. The exact mechanism of GH remains unknown, but fluctuations in blood glucose and insulin levels play important roles in promoting glycogen accumulation....

Full description

Bibliographic Details
Main Authors: Leila A. Alenazy, Muhammad Javed, Hussien Elsiesy, Emad Raddaoui, Waleed K. Al-Hamoudi
Format: Article
Language:English
Published: Hindawi Limited 2020-01-01
Series:Case Reports in Medicine
Online Access:http://dx.doi.org/10.1155/2020/1294074
id doaj-ef278e384c424fc598f55cf83c037a79
record_format Article
spelling doaj-ef278e384c424fc598f55cf83c037a792020-11-25T03:27:59ZengHindawi LimitedCase Reports in Medicine1687-96271687-96352020-01-01202010.1155/2020/12940741294074Glycogenic Hepatopathy: A Rare Hepatic Complication of Poorly Controlled Type 1 DMLeila A. Alenazy0Muhammad Javed1Hussien Elsiesy2Emad Raddaoui3Waleed K. Al-Hamoudi4Department of Gastroenterology and Hepatology Unit (59), Department of Medicine, King Saud University, Riyadh 11461, Saudi ArabiaDepartment of Gastroenterology and Hepatology Unit (59), Department of Medicine, King Saud University, Riyadh 11461, Saudi ArabiaDepartment of Liver Transplantation, King Faisal Specialist Hospital, Alfaisal University, Riyadh, Saudi ArabiaDepartment of Pathology, Alfaisal University, Riyadh, Saudi ArabiaDepartment of Gastroenterology and Hepatology Unit (59), Department of Medicine, King Saud University, Riyadh 11461, Saudi ArabiaGlycogen hepatopathy (GH) is a rare complication of type 1 diabetes mellitus that leads to an abnormal accumulation of glycogen in the hepatocytes. The exact mechanism of GH remains unknown, but fluctuations in blood glucose and insulin levels play important roles in promoting glycogen accumulation. We report a case of a 16-year-old female diagnosed with poorly controlled type 1 diabetes mellitus with hepatomegaly and elevated liver enzymes. The patient experienced multiple admissions for diabetic ketoacidosis, and she also had celiac disease diagnosed 2 years previously based on serology and a duodenal biopsy. The laboratory analyses results were compatible with acute hepatitis, and the celiac serology was positive. Other investigations ruled out viral hepatitis and autoimmune and metabolic liver diseases. Ultrasound and computerized tomography (CT) scans of the abdomen revealed liver enlargement with diffuse fatty infiltration. A liver biopsy revealed the presence of abundant glycogen in the cytoplasm of the hepatocytes. PAS staining was strongly positive, which confirmed the diagnosis of GH. There were no features of autoimmune hepatitis or significant fibrosis. Duodenal biopsy results were consistent with celiac disease. Despite our efforts, which are supported by a multidisciplinary team approach that included a hepatologist, a diabetic educator, a dietitian, and an endocrinologist, we have encountered difficulties in controlling the patient’s diabetes, and she persistently maintains symptomatic hepatomegaly and abnormal liver biochemistry. Given the patient’s age, we assumed that these abnormalities were related to patient noncompliance. In conclusion, GH remains an under-recognized complication of type 1 DM that is potentially reversible with adequate glycemic control. The awareness of GH should prevent diagnostic delay and its implications for management and the outcome.http://dx.doi.org/10.1155/2020/1294074
collection DOAJ
language English
format Article
sources DOAJ
author Leila A. Alenazy
Muhammad Javed
Hussien Elsiesy
Emad Raddaoui
Waleed K. Al-Hamoudi
spellingShingle Leila A. Alenazy
Muhammad Javed
Hussien Elsiesy
Emad Raddaoui
Waleed K. Al-Hamoudi
Glycogenic Hepatopathy: A Rare Hepatic Complication of Poorly Controlled Type 1 DM
Case Reports in Medicine
author_facet Leila A. Alenazy
Muhammad Javed
Hussien Elsiesy
Emad Raddaoui
Waleed K. Al-Hamoudi
author_sort Leila A. Alenazy
title Glycogenic Hepatopathy: A Rare Hepatic Complication of Poorly Controlled Type 1 DM
title_short Glycogenic Hepatopathy: A Rare Hepatic Complication of Poorly Controlled Type 1 DM
title_full Glycogenic Hepatopathy: A Rare Hepatic Complication of Poorly Controlled Type 1 DM
title_fullStr Glycogenic Hepatopathy: A Rare Hepatic Complication of Poorly Controlled Type 1 DM
title_full_unstemmed Glycogenic Hepatopathy: A Rare Hepatic Complication of Poorly Controlled Type 1 DM
title_sort glycogenic hepatopathy: a rare hepatic complication of poorly controlled type 1 dm
publisher Hindawi Limited
series Case Reports in Medicine
issn 1687-9627
1687-9635
publishDate 2020-01-01
description Glycogen hepatopathy (GH) is a rare complication of type 1 diabetes mellitus that leads to an abnormal accumulation of glycogen in the hepatocytes. The exact mechanism of GH remains unknown, but fluctuations in blood glucose and insulin levels play important roles in promoting glycogen accumulation. We report a case of a 16-year-old female diagnosed with poorly controlled type 1 diabetes mellitus with hepatomegaly and elevated liver enzymes. The patient experienced multiple admissions for diabetic ketoacidosis, and she also had celiac disease diagnosed 2 years previously based on serology and a duodenal biopsy. The laboratory analyses results were compatible with acute hepatitis, and the celiac serology was positive. Other investigations ruled out viral hepatitis and autoimmune and metabolic liver diseases. Ultrasound and computerized tomography (CT) scans of the abdomen revealed liver enlargement with diffuse fatty infiltration. A liver biopsy revealed the presence of abundant glycogen in the cytoplasm of the hepatocytes. PAS staining was strongly positive, which confirmed the diagnosis of GH. There were no features of autoimmune hepatitis or significant fibrosis. Duodenal biopsy results were consistent with celiac disease. Despite our efforts, which are supported by a multidisciplinary team approach that included a hepatologist, a diabetic educator, a dietitian, and an endocrinologist, we have encountered difficulties in controlling the patient’s diabetes, and she persistently maintains symptomatic hepatomegaly and abnormal liver biochemistry. Given the patient’s age, we assumed that these abnormalities were related to patient noncompliance. In conclusion, GH remains an under-recognized complication of type 1 DM that is potentially reversible with adequate glycemic control. The awareness of GH should prevent diagnostic delay and its implications for management and the outcome.
url http://dx.doi.org/10.1155/2020/1294074
work_keys_str_mv AT leilaaalenazy glycogenichepatopathyararehepaticcomplicationofpoorlycontrolledtype1dm
AT muhammadjaved glycogenichepatopathyararehepaticcomplicationofpoorlycontrolledtype1dm
AT hussienelsiesy glycogenichepatopathyararehepaticcomplicationofpoorlycontrolledtype1dm
AT emadraddaoui glycogenichepatopathyararehepaticcomplicationofpoorlycontrolledtype1dm
AT waleedkalhamoudi glycogenichepatopathyararehepaticcomplicationofpoorlycontrolledtype1dm
_version_ 1715207038231904256