J Rheum Dis.  2015 Jun;22(3):200-204. 10.4078/jrd.2015.22.3.200.

Hepatic Sarcoidosis in a Patient with Chronic Hepatitis B Virus Infection

Affiliations
  • 1Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
  • 2Department of Pathology, Yonsei University College of Medicine, Seoul, Korea.
  • 3Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea. sangwonlee@yuhs.ac
  • 4Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.

Abstract

Sarcoidosis is a systemic inflammatory granulomatous disease affecting multiple organs, including liver, spleen, heart, eyes, and skin. Liver involvement is reported in 11.5% of cases and many studies have reported on the association between hepatitis C virus infection and sarcoidosis. However, the role of hepatitis B virus (HBV) infection as a trigger for sarcoidosis has never been reported. We describe a case of hepatic sarcoidosis in a patient with chronic hepatitis B infection, with a possible link between the two. It is the first case report of a patient with interferon-alpha-naive chronic HBV infection presenting with hepatic sarcoidosis accompanied by portal hypertension and liver cirrhosis.

Keyword

Sarcoidosis; Hepatitis B virus; Liver cirrhosis; Portal hypertension

MeSH Terms

Heart
Hepacivirus
Hepatitis B virus
Hepatitis B, Chronic*
Humans
Hypertension, Portal
Liver
Liver Cirrhosis
Sarcoidosis*
Skin
Spleen

Figure

  • Figure 1. Abdomen sonogram (A) and abdomen computed tomography (CT) scan (B). Sonogram (A) reveals coarse parenchymal echogenicity of the liver. CT scan (B) shows heterogeneous enhancement in the enlarged liver and the spleen.

  • Figure 2. Liver biopsy showing the non-caseating granuloma (arrows) (A) and asteroid body (B). Special staining for acid fast bacilli (AFB) (C) and periodic acid Schiff (PAS) (D) were negative (A: H&E, ×100; B: H&E, ×400; C: AFB, ×400; D: PAS, ×400).

  • Figure 3. Positron emission tomography scan with multiple uptakes in the liver, spleen, lymph nodes, and bones.

  • Figure 4. Chest computed tomography (CT) scans (A, B) and abdominal CT scans (C, D). CT scans at the time of diagnosis (A, C) showing multiple perilymphatic nodules in both lungs (arrows) and heterogeneous enhancement in liver and spleen with hepatosplenomegaly. CT scans (B, D) taken after steroid treatment, revealing near total resolution of perilymphatic nodules and decreased size of liver and spleen.


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