Management of hepatic sarcoidosis

Background and Aims: Liver involvement in sarcoidosis may occur in up to 60% of all patients. As many patients experience only minor symptoms, a high number of undiagnosed cases must be assumed. In order to successfully identify patients with hepatic sarcoidosis, a throughout characterization of the...

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Hauptverfasser: Sollors, Janina (VerfasserIn) , Schlevogt, Bernhard (VerfasserIn) , Schmidt, Hartmut J. (VerfasserIn) , Wörns, Marcus-Alexander (VerfasserIn) , Galle, Peter R. (VerfasserIn) , Qian, Yuquan (VerfasserIn) , Antoni, Christoph Helmer (VerfasserIn) , Weis, Cleo-Aron Thias (VerfasserIn) , Hetjens, Svetlana (VerfasserIn) , Bergner, Raoul (VerfasserIn) , Ebert, Matthias (VerfasserIn) , Teufel, Andreas (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 15 Sep. 2022
In: Journal of gastrointestinal and liver diseases
Year: 2022, Jahrgang: 31, Heft: 3, Pages: 323-330
ISSN:1842-1121
DOI:10.15403/jgld-4122
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.15403/jgld-4122
Verlag, lizenzpflichtig, Volltext: https://www.jgld.ro/jgld/index.php/jgld/article/view/4122
Volltext
Verfasserangaben:Janina Sollors, Bernhard Schlevogt, Hartmut J. Schmidt, Marcus Wörns, Peter R. Galle, Yuquan Qian, Christoph Antoni, Cleo-Aron Weis, Svetlana Hetjens, Raoul Bergner, Matthias P. Ebert, Andreas Teufel
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Zusammenfassung:Background and Aims: Liver involvement in sarcoidosis may occur in up to 60% of all patients. As many patients experience only minor symptoms, a high number of undiagnosed cases must be assumed. In order to successfully identify patients with hepatic sarcoidosis, a throughout characterization of these patients and their course of disease is necessary. - Methods: We collected 40 patients from four German centers to evaluate current treatment standards and course of disease. All of our patients underwent liver biopsy with histologically proven granulomatous hepatitis. - Results: Detailed characterization of our patients showed an overall benign course of disease. Treatment was very diverse with glucocorticoids for 1 year in 55% (22/40), 5-10 years in 18% (7/40), and permanently in 18% (7/40). Other treatments included disease-modifying anti-rheumatic drugs (DMARDs), the conventional non-biological type in 53% of all patients (of these 81% received azathioprine, 46% metotrexate, 10% hydroxychloroquine, 10% mycophenolate mofetil and 10% cyclophosphamide and biologicals in 8%. Despite these very diverse treatments, patients generally showed slow progression of the disease. Two patients died. None of our patients received a liver transplantation. - Conclusions: Patients received diverse treatments and generally showed slow progression of the disease. Based on our experience, we proposed a diagnostic work up and surveillance strategy as a basis for future, prospective register studies.
Beschreibung:Gesehen am 18.01.2023
Beschreibung:Online Resource
ISSN:1842-1121
DOI:10.15403/jgld-4122