1997
DOI: 10.1097/00004836-199706000-00019
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Pyrazinamide-Induced Granulomatous Hepatitis

Abstract: Noncaseating granulomatous hepatitis may be caused by a variety of drugs, but we have not found, by computer search of the literature, a previous describe of granulomatous hepatitis associated with pyrazinamide. We describe a 52-year-old man with hectic fever, chills, extreme fatigue, liver damage, and hyperuricemia about 4 weeks after commencing pyrazinamide therapy. A liver biopsy specimen showed noncaseating epithelioid granulomas. The patient recovered soon after the interruption of tuberculostatic treatme… Show more

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Cited by 27 publications
(10 citation statements)
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“…Acute dose-related hepatocellular necroses have also been reported [52]. Of note, allopurinol decreases the clearance of pyrazinamide and increases the risk for toxicity.…”
Section: Pyrazinamidementioning
confidence: 95%
“…Acute dose-related hepatocellular necroses have also been reported [52]. Of note, allopurinol decreases the clearance of pyrazinamide and increases the risk for toxicity.…”
Section: Pyrazinamidementioning
confidence: 95%
“…7 However, it must be appreciated that this may well be an underestimate, because patients with drug reactions characterized by nonspecific liver dysfunction following a short period of drug ingestion do not usually undergo liver biopsy. There have recently been reports of hepatic granulomas induced by drugs that had not previously been considered to be causal of this condition, 11,[16][17][18][19][20] and we therefore believe that many more drugs may potentially play a role in the development of hepatic granuloma.…”
Section: Discussionmentioning
confidence: 91%
“…Hepatic granulomas may also develop during Hodgkin’s disease or sometimes even precede lymphomas 10 . In addition, GH may be caused by a variety of drugs 11–15 …”
Section: Discussionmentioning
confidence: 99%
“…10 In addition, GH may be caused by a variety of drugs. [11][12][13][14][15] Sarcoidosis is an idiopathic systemic inflammatory granulomatous disorder comprised of epithelioid and multinucleated giant cells with none or little necrosis. It usually invades the lungs with fibrosis and may also involve lymph nodes, skin, liver, spleen, eyes, phalangeal bones and parotid glands.…”
Section: Case Reportmentioning
confidence: 99%