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1.
BMJ Case Rep ; 20152015 May 04.
Article in English | MEDLINE | ID: mdl-25939971

ABSTRACT

A 27-year-old man developed extensive hepatic portal venous gas (HPVG) shortly after staging colonoscopy for active, ulcerating, terminal ileal Crohn's disease. Non-operative management was instigated with broad-spectrum antibiotics and thromboprophylaxis. Radiology at 72 h demonstrated resolution of HPVG but revealed fresh non-occlusive left portal vein thrombus. Anticoagulation with warfarin was continued for 1 year, during which the thrombus initially progressed and then organised with recanalisation of the portal vein. There were no long-term clinical consequences. HPVG has previously been documented as a rare complication of inflammatory bowel disease and endoscopic intervention. We hypothesise that the barotrauma sustained during endoscopy, in association with active ulceration and mucosal friability, predisposes to the influx of gas and bacteria into the portal system. We describe successful non-operative management of HPVG in this setting and draw attention to an additional complication of portal venous thrombosis, highlighting the importance of thromboprophylaxis and serial radiological examination.


Subject(s)
Colonoscopy/adverse effects , Crohn Disease/complications , Embolism, Air/etiology , Ileitis/complications , Portal Vein/diagnostic imaging , Venous Thrombosis/prevention & control , Adult , Anti-Bacterial Agents/therapeutic use , Anticoagulants/therapeutic use , Crohn Disease/drug therapy , Embolism, Air/complications , Embolism, Air/diagnostic imaging , Humans , Ileitis/drug therapy , Liver/blood supply , Liver/diagnostic imaging , Male , Portal Vein/drug effects , Portal Vein/pathology , Prognosis , Tomography, X-Ray Computed , Treatment Outcome , Venous Thrombosis/drug therapy , Venous Thrombosis/etiology , Warfarin/therapeutic use
2.
World J Gastroenterol ; 20(46): 17352-9, 2014 Dec 14.
Article in English | MEDLINE | ID: mdl-25516646

ABSTRACT

Abnormalities in liver function tests, including transient and self-limiting hypertransaminasemia, cholestatic disease and hepatitis, can develop during treatment with anti-tumour-necrosis-factor (TNF) therapy. The optimal management of liver injury related to anti-TNF therapy is still a matter of debate. Although some authors recommend discontinuing treatment in case of both a rise of alanine aminotransferase more than 5 times the upper limit of normal, or the occurrence of jaundice, there are no standard guidelines for the management of anti-TNF-related liver injury. Bibliographical searches were performed in PubMed, using the following key words: inflammatory bowel disease (IBD); TNF inhibitors; hypertransaminasemia; drug-related liver injury; infliximab. According to published data, elevation of transaminases in patients with IBD treated with anti-TNF is a common finding, but resolution appears to be the usual outcome. Anti-TNF agents seem to be safe with a low risk of causing severe drug-related liver injury. According to our centre experience, we found that hypertransaminasemia was a common, mainly self-limiting finding in our IBD cohort and was not correlated to infliximab treatment on both univariate and multivariate analyses. An algorithm for the management of liver impairment occurring during anti-TNF treatment is also proposed and this highlights the need of a multidisciplinary approach and suggests liver biopsy as a key-point in the management decision in case of severe rise of transaminases. However, hepatic injury is generally self-limiting and drug withdrawal seems to be an exception.


Subject(s)
Anti-Inflammatory Agents/adverse effects , Biological Products/adverse effects , Chemical and Drug Induced Liver Injury/etiology , Liver/drug effects , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Algorithms , Animals , Chemical and Drug Induced Liver Injury/diagnosis , Chemical and Drug Induced Liver Injury/immunology , Chemical and Drug Induced Liver Injury/metabolism , Chemical and Drug Induced Liver Injury/therapy , Critical Pathways , Humans , Liver/immunology , Liver/metabolism , Liver Function Tests , Practice Guidelines as Topic , Predictive Value of Tests , Risk Assessment , Risk Factors , Tumor Necrosis Factor-alpha/immunology , Tumor Necrosis Factor-alpha/metabolism
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