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Glimepiride-induced cholestasis in a man with diabetes mellitus: a case report
INTRODUCTION: There has been a progressive increase in the incidence of type II diabetes mellitus cases over the past decade. The availability of a wide variety of oral hypoglycemics has given rise to a number of adverse effects. In this case report, we describe the case of a patient recently diagno...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2827158/ http://dx.doi.org/10.4076/1752-1947-3-9257 |
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author | Omar, Hesham Kolla, Jaya Mangar, Devanand Camporesi, Enrico |
author_facet | Omar, Hesham Kolla, Jaya Mangar, Devanand Camporesi, Enrico |
author_sort | Omar, Hesham |
collection | PubMed |
description | INTRODUCTION: There has been a progressive increase in the incidence of type II diabetes mellitus cases over the past decade. The availability of a wide variety of oral hypoglycemics has given rise to a number of adverse effects. In this case report, we describe the case of a patient recently diagnosed with type II diabetes. He was receiving treatment with glimepiride and experienced rapid onset of cholestatic liver injury as a side effect, which reversed upon cessation of therapy. CASE PRESENTATION: We present the case of a 58-year-old Egyptian man with a recent diagnosis of type II diabetes mellitus. He presented with a clinical picture of progressive jaundice three days before admission. Laboratory investigations revealed elevated bilirubin, alkaline phosphatase and gamma glutamyl transferase levels. Ultrasonography revealed intrahepatic biliary duct dilatation and two small lymph nodes in the porta hepatis; there was, however, no extrahepatic biliary duct dilatation or stones in the gall bladder. Abdominal computed tomography excluded pancreatic or hepatic focal lesions, but the tumor marker CA19-9 was elevated. The progressive improvement in the patient's symptomatology and laboratory investigations after admission argued against malignancy. A thorough and detailed history revealed that the patient had started on a new medication, glimepiride, five months earlier for the treatment of diabetes mellitus and an improvement was noted after discontinuation of this oral hypoglycemic and the introduction of insulin therapy to control his blood sugar. CONCLUSION: Drugs are an important, often unrecognized, cause of acute cholestasis. Among the rare causes responsible for this complication is the sulfonylurea glimepiride. A thorough drug history is therefore helpful in any case of unexplained cholestasis. |
format | Text |
id | pubmed-2827158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28271582010-02-24 Glimepiride-induced cholestasis in a man with diabetes mellitus: a case report Omar, Hesham Kolla, Jaya Mangar, Devanand Camporesi, Enrico J Med Case Reports Case report INTRODUCTION: There has been a progressive increase in the incidence of type II diabetes mellitus cases over the past decade. The availability of a wide variety of oral hypoglycemics has given rise to a number of adverse effects. In this case report, we describe the case of a patient recently diagnosed with type II diabetes. He was receiving treatment with glimepiride and experienced rapid onset of cholestatic liver injury as a side effect, which reversed upon cessation of therapy. CASE PRESENTATION: We present the case of a 58-year-old Egyptian man with a recent diagnosis of type II diabetes mellitus. He presented with a clinical picture of progressive jaundice three days before admission. Laboratory investigations revealed elevated bilirubin, alkaline phosphatase and gamma glutamyl transferase levels. Ultrasonography revealed intrahepatic biliary duct dilatation and two small lymph nodes in the porta hepatis; there was, however, no extrahepatic biliary duct dilatation or stones in the gall bladder. Abdominal computed tomography excluded pancreatic or hepatic focal lesions, but the tumor marker CA19-9 was elevated. The progressive improvement in the patient's symptomatology and laboratory investigations after admission argued against malignancy. A thorough and detailed history revealed that the patient had started on a new medication, glimepiride, five months earlier for the treatment of diabetes mellitus and an improvement was noted after discontinuation of this oral hypoglycemic and the introduction of insulin therapy to control his blood sugar. CONCLUSION: Drugs are an important, often unrecognized, cause of acute cholestasis. Among the rare causes responsible for this complication is the sulfonylurea glimepiride. A thorough drug history is therefore helpful in any case of unexplained cholestasis. BioMed Central 2009-09-15 /pmc/articles/PMC2827158/ http://dx.doi.org/10.4076/1752-1947-3-9257 Text en Copyright ©2009 Omar et al.; licensee Cases Network Ltd. licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case report Omar, Hesham Kolla, Jaya Mangar, Devanand Camporesi, Enrico Glimepiride-induced cholestasis in a man with diabetes mellitus: a case report |
title | Glimepiride-induced cholestasis in a man with diabetes mellitus: a case report |
title_full | Glimepiride-induced cholestasis in a man with diabetes mellitus: a case report |
title_fullStr | Glimepiride-induced cholestasis in a man with diabetes mellitus: a case report |
title_full_unstemmed | Glimepiride-induced cholestasis in a man with diabetes mellitus: a case report |
title_short | Glimepiride-induced cholestasis in a man with diabetes mellitus: a case report |
title_sort | glimepiride-induced cholestasis in a man with diabetes mellitus: a case report |
topic | Case report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2827158/ http://dx.doi.org/10.4076/1752-1947-3-9257 |
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