Glycogenic Hepatopathy in a 19- year-old Male with Uncontrolled Insulin Dependent Diabetes: Clinical Presentation and Review of Literature
Glycogenic Hepatopathy (GH) is a rare entity encountered in patients with poorly controlled insulin-dependent diabetes. GH results from excessive accumulation of glycogen in the hepatocytes and is characterised by tender hepatomegaly and transaminitis. Hyperglycaemia in these patients leads to frequ...
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doaj-5f514b6ad4c1400785d75f82ee1eb3992020-11-25T02:08:01ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2018-01-01121OD07OD11 10.7860/JCDR/2018/27279.11029Glycogenic Hepatopathy in a 19- year-old Male with Uncontrolled Insulin Dependent Diabetes: Clinical Presentation and Review of LiteratureDustin L Little0Creticus Petrov Marak1Achuta Kumar Guddati2William G Simpson3DO, Department of Family Medicine, Tahlequah City Hospital, Tahlequah, Oklahoma, USA.MD, Department of Critical Care, Tahlequah City Hospital, Tahlequah, Oklahoma, USA.MD, PhD, Department of Haematology and Oncology, SUNY Downstate Medical Center, Brooklyn, New York, USA.MD, Department of Gastroenterology, Tahlequah City Hospital, Tahlequah, Oklahoma, USA.Glycogenic Hepatopathy (GH) is a rare entity encountered in patients with poorly controlled insulin-dependent diabetes. GH results from excessive accumulation of glycogen in the hepatocytes and is characterised by tender hepatomegaly and transaminitis. Hyperglycaemia in these patients leads to frequent use of high doses of insulin. High plasma levels of both serum glucose and insulin causes increased production and storage of glycogen in the hepatocytes. We present the clinical course and management of a patient who presented with hyperglycaemia and was found to have glycaemic hepatopathy. The presentation of similar cases that have been reported in medical literature has been reviewed and discussed in this review. GH is an underdiagnosed entity and should be considered in the differentials of any patient presenting with hepatomegaly and transaminitis, particularly among uncontrolled diabetics.https://jcdr.net/articles/PDF/11029/27279_131017_27279_F(RK)_PFI_(BT_PB_SG_VG)_PFA(GG)_PB(MJ_AP)_PN(AP).pdfdiabetes mellitusglycogen storage diseasehepatomegaly |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Dustin L Little Creticus Petrov Marak Achuta Kumar Guddati William G Simpson |
spellingShingle |
Dustin L Little Creticus Petrov Marak Achuta Kumar Guddati William G Simpson Glycogenic Hepatopathy in a 19- year-old Male with Uncontrolled Insulin Dependent Diabetes: Clinical Presentation and Review of Literature Journal of Clinical and Diagnostic Research diabetes mellitus glycogen storage disease hepatomegaly |
author_facet |
Dustin L Little Creticus Petrov Marak Achuta Kumar Guddati William G Simpson |
author_sort |
Dustin L Little |
title |
Glycogenic Hepatopathy in a 19- year-old Male with Uncontrolled Insulin Dependent Diabetes: Clinical Presentation and Review of Literature |
title_short |
Glycogenic Hepatopathy in a 19- year-old Male with Uncontrolled Insulin Dependent Diabetes: Clinical Presentation and Review of Literature |
title_full |
Glycogenic Hepatopathy in a 19- year-old Male with Uncontrolled Insulin Dependent Diabetes: Clinical Presentation and Review of Literature |
title_fullStr |
Glycogenic Hepatopathy in a 19- year-old Male with Uncontrolled Insulin Dependent Diabetes: Clinical Presentation and Review of Literature |
title_full_unstemmed |
Glycogenic Hepatopathy in a 19- year-old Male with Uncontrolled Insulin Dependent Diabetes: Clinical Presentation and Review of Literature |
title_sort |
glycogenic hepatopathy in a 19- year-old male with uncontrolled insulin dependent diabetes: clinical presentation and review of literature |
publisher |
JCDR Research and Publications Private Limited |
series |
Journal of Clinical and Diagnostic Research |
issn |
2249-782X 0973-709X |
publishDate |
2018-01-01 |
description |
Glycogenic Hepatopathy (GH) is a rare entity encountered in patients with poorly controlled insulin-dependent diabetes. GH results from excessive accumulation of glycogen in the hepatocytes and is characterised by tender hepatomegaly and transaminitis. Hyperglycaemia in these patients leads to frequent use of high doses of insulin. High plasma levels of both serum glucose and insulin causes increased production and storage of glycogen in the hepatocytes. We present the clinical course and management of a patient who presented with hyperglycaemia and was found to have glycaemic hepatopathy. The presentation of similar cases that have been reported in medical literature has been reviewed and discussed in this review. GH is an underdiagnosed entity and should be considered in the differentials of any patient presenting with hepatomegaly and transaminitis, particularly among uncontrolled diabetics. |
topic |
diabetes mellitus glycogen storage disease hepatomegaly |
url |
https://jcdr.net/articles/PDF/11029/27279_131017_27279_F(RK)_PFI_(BT_PB_SG_VG)_PFA(GG)_PB(MJ_AP)_PN(AP).pdf |
work_keys_str_mv |
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1724928108415418368 |