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Budesonide with Low-Dose 6-Mercaptopurine as a Possible New Treatment for IgG4-Related Sclerosing Cholangitis and Systemic IgG4-Related Disease: A Case Report

Patient: Male, 70-year-old Final Diagnosis: Drug induced hepatopathy • gangrenous cholecystitis • IgG4 related sclerosing cholangitis • systemic IgG4 related disease Symptoms: Abdominal pain • jaundice Medication: — Clinical Procedure: Computed tomography • magnetic resonance cholangiopancreatograph...

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Autores principales: Gummlich, Benjamin Peter Michael, Hosseini, Ali Seif Amir, Schwörer, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745840/
https://www.ncbi.nlm.nih.gov/pubmed/36476942
http://dx.doi.org/10.12659/AJCR.938272
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author Gummlich, Benjamin Peter Michael
Hosseini, Ali Seif Amir
Schwörer, Harald
author_facet Gummlich, Benjamin Peter Michael
Hosseini, Ali Seif Amir
Schwörer, Harald
author_sort Gummlich, Benjamin Peter Michael
collection PubMed
description Patient: Male, 70-year-old Final Diagnosis: Drug induced hepatopathy • gangrenous cholecystitis • IgG4 related sclerosing cholangitis • systemic IgG4 related disease Symptoms: Abdominal pain • jaundice Medication: — Clinical Procedure: Computed tomography • magnetic resonance cholangiopancreatography Specialty: Gastroenterology and Hepatology OBJECTIVE: Rare disease BACKGROUND: Systemic IgG4-related disease is a rare disease that can affect the hepatobiliary system and may lead to tissue fibrosis and organ failure. Diagnostic criteria for IgG4-related disease are well established, and systemic glucocorticoids are recommended for initiation of treatment. Besides the beneficial properties of glucocorticoids, the long-term treatment with systemic steroids carries the risk of toxicity, especially in elderly patients, in whom IgG4-related disease is more common. Furthermore, disease relapses may occur during the tapering of steroids. Overall, the optimal treatment approach for maintenance therapy has not been clarified yet and is an area of current clinical research. CASE REPORT: We present a patient with IgG4-related sclerosing cholangitis and histologically confirmed systemic (multi-organ) IgG4-related disease who was at increased risk of disease recurrence. The effects of immunosuppressants (prednisolone, 6-mercaptopurine, budesonide) on clinical symptoms, laboratory parameters (AST, ALT, AP, γGT, bilirubin), and imaging examinations (magnetic resonance cholangiography) were documented over 56 months. Control of IgG4-related sclerosing cholangitis was achieved – without systemic prednisolone – with the locally acting glucocorticoid budesonide in combination with low-dose 6-mercaptopurine. During treatment with 6-mercaptopurine, transient hepatotoxicity occurred, which was reversed by intermittent pausing and subsequent dose reduction. In addition, gangrenous cholecystitis occurred as a complication of immunosuppression and was treated by emergency cholecystectomy. CONCLUSIONS: Budesonide could be a new treatment modality for IgG4-related sclerosing cholangitis. Systemic manifestations of immunoglobulin G4-related disease can be controlled with low-dose 6-mercaptopurine. Gangrenous cholecystitis may occur as a complication of immunosuppressive treatment.
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spelling pubmed-97458402022-12-19 Budesonide with Low-Dose 6-Mercaptopurine as a Possible New Treatment for IgG4-Related Sclerosing Cholangitis and Systemic IgG4-Related Disease: A Case Report Gummlich, Benjamin Peter Michael Hosseini, Ali Seif Amir Schwörer, Harald Am J Case Rep Articles Patient: Male, 70-year-old Final Diagnosis: Drug induced hepatopathy • gangrenous cholecystitis • IgG4 related sclerosing cholangitis • systemic IgG4 related disease Symptoms: Abdominal pain • jaundice Medication: — Clinical Procedure: Computed tomography • magnetic resonance cholangiopancreatography Specialty: Gastroenterology and Hepatology OBJECTIVE: Rare disease BACKGROUND: Systemic IgG4-related disease is a rare disease that can affect the hepatobiliary system and may lead to tissue fibrosis and organ failure. Diagnostic criteria for IgG4-related disease are well established, and systemic glucocorticoids are recommended for initiation of treatment. Besides the beneficial properties of glucocorticoids, the long-term treatment with systemic steroids carries the risk of toxicity, especially in elderly patients, in whom IgG4-related disease is more common. Furthermore, disease relapses may occur during the tapering of steroids. Overall, the optimal treatment approach for maintenance therapy has not been clarified yet and is an area of current clinical research. CASE REPORT: We present a patient with IgG4-related sclerosing cholangitis and histologically confirmed systemic (multi-organ) IgG4-related disease who was at increased risk of disease recurrence. The effects of immunosuppressants (prednisolone, 6-mercaptopurine, budesonide) on clinical symptoms, laboratory parameters (AST, ALT, AP, γGT, bilirubin), and imaging examinations (magnetic resonance cholangiography) were documented over 56 months. Control of IgG4-related sclerosing cholangitis was achieved – without systemic prednisolone – with the locally acting glucocorticoid budesonide in combination with low-dose 6-mercaptopurine. During treatment with 6-mercaptopurine, transient hepatotoxicity occurred, which was reversed by intermittent pausing and subsequent dose reduction. In addition, gangrenous cholecystitis occurred as a complication of immunosuppression and was treated by emergency cholecystectomy. CONCLUSIONS: Budesonide could be a new treatment modality for IgG4-related sclerosing cholangitis. Systemic manifestations of immunoglobulin G4-related disease can be controlled with low-dose 6-mercaptopurine. Gangrenous cholecystitis may occur as a complication of immunosuppressive treatment. International Scientific Literature, Inc. 2022-12-08 /pmc/articles/PMC9745840/ /pubmed/36476942 http://dx.doi.org/10.12659/AJCR.938272 Text en © Am J Case Rep, 2022 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Gummlich, Benjamin Peter Michael
Hosseini, Ali Seif Amir
Schwörer, Harald
Budesonide with Low-Dose 6-Mercaptopurine as a Possible New Treatment for IgG4-Related Sclerosing Cholangitis and Systemic IgG4-Related Disease: A Case Report
title Budesonide with Low-Dose 6-Mercaptopurine as a Possible New Treatment for IgG4-Related Sclerosing Cholangitis and Systemic IgG4-Related Disease: A Case Report
title_full Budesonide with Low-Dose 6-Mercaptopurine as a Possible New Treatment for IgG4-Related Sclerosing Cholangitis and Systemic IgG4-Related Disease: A Case Report
title_fullStr Budesonide with Low-Dose 6-Mercaptopurine as a Possible New Treatment for IgG4-Related Sclerosing Cholangitis and Systemic IgG4-Related Disease: A Case Report
title_full_unstemmed Budesonide with Low-Dose 6-Mercaptopurine as a Possible New Treatment for IgG4-Related Sclerosing Cholangitis and Systemic IgG4-Related Disease: A Case Report
title_short Budesonide with Low-Dose 6-Mercaptopurine as a Possible New Treatment for IgG4-Related Sclerosing Cholangitis and Systemic IgG4-Related Disease: A Case Report
title_sort budesonide with low-dose 6-mercaptopurine as a possible new treatment for igg4-related sclerosing cholangitis and systemic igg4-related disease: a case report
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745840/
https://www.ncbi.nlm.nih.gov/pubmed/36476942
http://dx.doi.org/10.12659/AJCR.938272
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