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Review
. 2016 Mar 14;22(10):2906-14.
doi: 10.3748/wjg.v22.i10.2906.

De novo autoimmune hepatitis in liver transplant: State-of-the-art review

Affiliations
Review

De novo autoimmune hepatitis in liver transplant: State-of-the-art review

Ranka Vukotic et al. World J Gastroenterol. .

Abstract

In the two past decades, a number of communications, case-control studies, and retrospective reports have appeared in the literature with concerns about the development of a complex set of clinical, laboratory and histological characteristics of a liver graft dysfunction that is compatible with autoimmune hepatitis. The de novo prefix was added to distinguish this entity from a pre-transplant primary autoimmune hepatitis, but the globally accepted criteria for the diagnosis of autoimmune hepatitis have been adopted in the diagnostic algorithm. Indeed, de novo autoimmune hepatitis is characterized by the typical liver necro-inflammation that is rich in plasma cells, the presence of interface hepatitis and the consequent laboratory findings of elevations in liver enzymes, increases in serum gamma globulin and the appearance of non-organ specific auto-antibodies. Still, the overall features of de novo autoimmune hepatitis appear not to be attributable to a univocal patho-physiological pathway because they can develop in the patients who have undergone liver transplantation due to different etiologies. Specifically, in subjects with hepatitis C virus recurrence, an interferon-containing antiviral treatment has been indicated as a potential inception of immune system derangement. Herein, we attempt to review the currently available knowledge about de novo liver autoimmunity and its clinical management.

Keywords: Antiviral therapy; Autoimmunity; De novo autoimmune hepatitis; Differential diagnosis; Hepatitis C virus recurrence; Liver transplant; Plasma-cell hepatitis.

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Figures

Figure 1
Figure 1
The portal tract. A: A moderate plasmacellular infiltrate. There is moderate interface hepatitis. The bile duct is regular. HE staining, 10 ×; B: A moderate chronic inflammatory infiltrate with plasma-cells. There is moderate interface hepatitis. The bile duct is regular. HE staining, 20 ×.
Figure 2
Figure 2
The lobule shows hepatocellular rosettas. HE staining, 20 ×.

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