CEN Case Reports

, Volume 2, Issue 1, pp 28–33

De novo acute hepatitis B in myeloperoxidase-specific anti-neutrophil cytoplasmic autoantibody-related microscopic polyangiitis treated with corticosteroids

  • Yoichi Iwafuchi
  • Yuko Oyama
  • Takashi Morita
  • Akira Kamimura
  • Shigeru Miyazaki
  • Ichiei Narita
Case Report

DOI: 10.1007/s13730-012-0033-2

Cite this article as:
Iwafuchi, Y., Oyama, Y., Morita, T. et al. CEN Case Rep (2013) 2: 28. doi:10.1007/s13730-012-0033-2
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Abstract

An 82-year-old female was referred to our hospital because of low-grade fever, anemia, and rapidly progressive nephritic syndrome. Her laboratory data showed mild proteinuria, mild renal failure, and the presence of myeloperoxidase-specific anti-neutrophil cytoplasmic autoantibody. A skin biopsy specimen taken from the erythematous purpura revealed neutrophilic infiltration around the blood vessels with fibrinoid changes in the vessel walls. A renal biopsy specimen revealed segmental necrotizing glomerulonephritis with fibro-cellular crescent formation without deposits of immunoglobulin or complement components, indicating microscopic polyangiitis. The use of corticosteroid treatment, including intravenous methylprednisolone, improved renal failure. After 4 years with low-dose maintenance corticosteroid therapy, she developed de novo acute hepatitis B, and entecavir was remarkably effective, showing a rapid recovery from liver dysfunction with jaundice. To prevent hepatitis B virus (HBV) reactivation and de novo acute hepatitis B induced by immunosuppressive or cytotoxic therapy, including corticosteroids alone, the measurement of HBV-related serological markers needs to be performed prior to the initiation of such therapy, even in renal diseases.

Keywords

Hepatitis B virus reactivationDe novo acute hepatitis BMicroscopic polyangiitisCorticosteroidsImmunosuppressive or cytotoxic therapyEntecavir

Introduction

Hepatitis B is the most common serious liver infection in the world. Approximately one-third of the world’s population has been infected at one point in their lives, including 350 million people who are chronic carriers. The majority of carriers who develop hepatitis B e antigen (HBeAg) seroconversion remain HBeAg-negative and hepatitis B e antibody (HBeAb)-positive, with normal alanine aminotransferase (ALT) levels and minimal or no necroinflammation on liver biopsy. This has been referred to as the “inactive carrier state” [1]. Hepatitis B virus (HBV) reactivation is a well-known phenomenon in chronic HBV carriers and it represents a life-threatening complication following cytotoxic or other immunosuppressive anticancer therapy. Furthermore, in hepatitis B surface antigen (HBsAg)-negative patients, the presence of hepatitis B core antibody (HBcAb), irrespective of the detection of hepatitis B surface antibody (HBsAb), is correlated with a significant risk of de novo hepatitis B infection following cytotoxic or immunosuppressive therapy [2]; however, following simple corticosteroid therapy, these pathophysiological phenomena will infrequently occur. We report a female with myeloperoxidase-specific anti-neutrophil cytoplasmic autoantibody (MPO-ANCA)-related microscopic polyangiitis (MPA) who developed de novo acute hepatitis B (DNH) following simple corticosteroid therapy.

Case report

An 82-year-old female was referred to our hospital because of low-grade fever, anemia, and rapidly progressive nephritic syndrome. She had hypertension, which was treated with amlodipine and losartan for 5 years, but had been in good health until 12 weeks before admission, when she noted low-grade fever and anorexia. She was admitted to a nearby hospital because of low-grade fever and arthralgia of 3 weeks duration. Her serum creatinine (Cre) level was 0.75 mg/dl and estimated glomerular filtration rate (eGFR) was 55.4 ml/min/1.73 m2 at first. She was treated with antibiotics, but her fever persisted, and her Cre level gradually became elevated to 1.47 mg/dl (eGFR 26.6 ml/min/1.73 m2). Rapidly progressive nephritic syndrome was suspected and she was found to be positive for MPO-ANCA. Therefore, she was transferred to our hospital for treatment.

On examination, the patient’s blood pressure was 136/80 mmHg, pulse was 92 beats/min, and temperature was 37.3 °C. She was slightly anemic and not icteric. The heart and lungs were normal, the liver and spleen were not palpable, and lymph nodes were not palpable. An erythematous purpura was observed and mild peripheral edema was present.

Urinary protein was 0.3–0.7 g/24 h and the urinary sediment showed 1–4 erythrocytes and 1–4 leukocytes per high-power field. Her hematocrit level was 23.0 %, hemoglobin concentration was 7.5 g/dl, platelet count was 489,000/μl, and leukocyte count was 19,370/μl. The serum urea nitrogen (UN) level was 45.5 mg/dl, the Cre level was 2.35 mg/dl, the eGFR was 15.9 ml/min/1.73 m2, the uric acid (UA) level was 8.8 mg/dl, the cholesterol level was 117 mg/dl, the total protein level was 7.2 g/dl, the albumin level was 2.2 g/dl, the total bilirubin level was 0.23 mg/dl, the aspartate aminotransferase (AST) level was 42 IU/l, the ALT level was 29 IU/l, the lactate dehydrogenase (LDH) level was 158 IU/l, the alkaline phosphatase (ALP) level was 399 IU/l, and the gamma glutamyl transpeptidase (GGT) level was 22 IU/l. The C-reactive protein (CRP) level was 10.22 mg/dl, IgG was 1261 mg/dl, IgA was 255 mg/dl, IgM was 87 mg/dl, and ferritin was 333 ng/ml. Serum C3, C4, and total serum hemolytic activity were normal. Circulating immune complexes were negative. MPO-ANCA was positive with a titer of 80 EU, but anti-proteinase3-specific ANCA was negative. Anti-glomerular basement membrane antibody was negative. Rheumatoid factor, antistreptolysin-O, HBsAg, hepatitis C virus (HCV) antibody, human immunodeficiency virus antibody, antinuclear antibody, and cryoglobulin were all negative. A chest X-ray showed mild cardiomegaly and an electrocardiogram showed ST segment depressions of V2 and V3. Renal echogram and computed tomography showed kidneys which were normal in size.

Therefore, we promptly initiated a 3-day course of intravenous methylprednisolone (500 mg/day) followed by oral prednisolone (PSL) at 20 mg/day. After this therapy, the patient’s symptoms, including low-grade fever, anorexia, and skin lesions, rapidly diminished, along with a decrease in CRP levels to within the normal range. A skin biopsy specimen taken from the erythematous purpura revealed neutrophilic infiltration around the blood vessels, with fibrinoid changes in the vessel walls. On the 20th hospital day, a renal biopsy was performed to investigate the cause of rapidly progressive nephritic syndrome. Under light microscopy, 28 glomeruli were found, eight were obsoleted and seven were obsoleting with collapsed tufts. Four glomeruli showed segmental sclerosing changes with small fibro-cellular crescent, and one glomerulus had segmental necrotizing changes involving vas afferens with small cellular crescents (Fig. 1). The remaining glomeruli, except for a few showing mild ischemic changes, appeared almost normal. There were several focal areas of severe interstitial changes with cellular infiltration and tubular damages. Obsoleted and obsoleting glomeruli were located mainly in these areas, and glomeruli with mild changes in the areas also had mildly collapsing tufts (Fig. 2). Active vasculitis with fibrinoid change was not found, but there was a distorted artery with disruption of the internal elastic lamina. These findings were interpreted as compatible with those of segmental necrotizing glomerulonephritis of 15 weeks old but still active. By immunofluorescence study, no significant deposits of immunoglobulins or complement components were found. Based on the skin and renal histological findings and laboratory findings, the patient was diagnosed as having MPA. Eight weeks after admission, oral PSL was tapered off to 15 mg daily and, after 1 week, she was discharged. At that time, her Cre level was 1.26 mg/dl (eGFR, 31.4 ml/min/1.73 m2), and then she was treated in our outpatient clinic once a month. Almost every 4 weeks, a routine blood and urine test was performed to investigate the presence of exacerbation of renal function. Approximately 4 years after admission, PSL was slowly tapered off to 5 mg daily (Fig. 3).
https://static-content.springer.com/image/art%3A10.1007%2Fs13730-012-0033-2/MediaObjects/13730_2012_33_Fig1_HTML.jpg
Fig. 1

One glomerulus showing segmental necrotizing changes involving the vas afferens and small cellular crescents (periodic acid methenamine silver)

https://static-content.springer.com/image/art%3A10.1007%2Fs13730-012-0033-2/MediaObjects/13730_2012_33_Fig2_HTML.jpg
Fig. 2

An area of severe interstitial changes with cellular infiltration and tubular damages, where obsoleted and obsoleting glomeruli are located and two glomeruli (arrows) have mildly collapsing tufts and lamellated Bowman’s capsule (periodic acid methenamine silver)

https://static-content.springer.com/image/art%3A10.1007%2Fs13730-012-0033-2/MediaObjects/13730_2012_33_Fig3_HTML.gif
Fig. 3

The clinical course of the patient. Entecavir was remarkably effective, and the patient showed a rapid recovery from liver dysfunction with jaundice. PSL prednisolone, M-PSL Pulse intravenous methylprednisolone pulse therapy, T.Bil total bilirubin, AST aspartate aminotransferase, GGT gamma glutamyl transpeptidase, HD hemodialysis

Six weeks before the second admission, PSL was tapered off to 3 mg from 5 mg daily. Approximately 4 weeks later, the patient developed anorexia and was easily fatigued. Shortly thereafter, she developed jaundice on her conjunctivae and skin. Therefore, she was admitted to our hospital again for further evaluation and treatment. Physical examination showed mild jaundice and bilateral pretibial edema. The liver and spleen were not palpable. Her laboratory data showed acute exacerbation of chronic renal failure and severe liver biochemistry as follows: UN, 139.5 mg/dl; Cre, 9.74 mg/dl; eGFR, 3.3 ml/min/1.73 m2; UA, 10.5 mg/dl; total bilirubin, 5.65 mg/dl; direct bilirubin, 3.93 mg/dl; AST, 630 IU/l; ALT, 655 IU/l; LDH, 506 IU/l; ALP, 368 IU/l; and GGT, 320 IU/l. Using the frozen serum, which was taken at the first admission, we re-checked the HBsAg, HBV DNA, and anti-HCV results, which were all negative, but the HBsAb and HBcAb results were positive. Furthermore, HBsAg was positive in her serum at the second admission, whereas anti-HBc IgM was negative, indicating that this acute hepatitis B was caused by HBV reactivation. The titer of HBV DNA was high at 7.6 log copies/ml. Based on the diagnosis of DNH, which was caused by the reactivation of HBV, an oral weekly dose (0.5 mg) of entecavir was immediately started on the second hospital day. Following entecavir administration, the serum HBV DNA level gradually fell and became undetectable at 4 weeks, and transaminase and bilirubin levels gradually fell to within the normal range at 5 weeks (Fig. 3) The patient’s renal function temporarily deteriorated. Consequently, she received hemodialysis treatment three times a week during the following 2 weeks. We concluded that MPA did not recur because MPO-ANCA levels remained undetectable on this admission. Therefore, we considered that the main causes of her acute exacerbation of chronic renal failure were dehydration and hepato-renal syndrome as a result of DNH. The patient was discharged on the 52nd hospital day. At that time, the level of HBV DNA in her serum remained under the lower limit of detection, and transaminase and bilirubin levels were normal. Her renal function returned to its previous level (Cre, 2.05 mg/dl; eGFR, 18.2 ml/min/1.73 m2). She was then treated in our outpatient clinic once a month again, and entecavir administration was continued. After the administration of entecavir, the level of HBV DNA in the serum remained negative. However, her renal function slowly deteriorated. Approximately 16 months after her second admission, her Cre level reached 4.56 mg/dl (eGFR, 7.6 ml/min/1.73 m2) and her heart failure worsened and, therefore, she began receiving maintenance hemodialysis. She continued maintenance hemodialysis for approximately 2 years until death due to congestive heart failure, and liver dysfunction was not observed by this time.

Discussion

Reactivation of HBV is becoming a well-recognized complication in patients with chronic HBV infection who are undergoing immunosuppressive or cytotoxic therapy [2]. The reactivation of HBV replication with an increase in serum HBV DNA and ALT levels has been reported in 20–50 % of hepatitis B carriers undergoing immunosuppressive or cancer chemotherapy [1]. The risk of HBV reactivation is much lower in patients with resolved infection, but the reactivation of HBV has been reported not only in HBsAg-positive patients undergoing immunosuppressive or cytotoxic therapy, but also in a proportion of HBsAg-negative patients with HBc antibody and/or HBs antibody. Currently, there is insufficient information to recommend routine prophylaxis for these individuals [1, 3]. Furthermore, DNH is defined as hepatitis B occurring in a patient who has an HBsAb- and/or HBcAb-positive status by HBV reactivation; DNH can be induced by immunosuppressive or cytotoxic therapy. Cases of fatal DNH following immunosuppressive or cytotoxic therapy for some diseases have been reported [4].

Microscopic polyangiitis is a type of vasculitis that affects small blood vessels, such as capillaries, venules, or arterioles. ANCA-positive MPA should be considered as part of the spectrum of ANCA-associated small-vessel vasculitis, ranging from renal-limited rapidly progressive glomerulonephritis (RPGN) to multisystem diseases, including Wegener’s granulomatosis and Churg–Strauss syndrome [5, 6]. Corticosteroids are frequently used in the treatment of ANCA-positive RPGN. In 2002, Sakai et al. [7] published a Japanese version of the RPGN clinical guidelines based on data for 715 RPGN patents collected until 2001. Yamagata, who was a coauthor of the guidelines (2nd edition) in 2011, and colleagues reported that an oral PSL dose <0.8 mg/kg/day with or without cyclophosphamide as an initial treatment could improve patient survival in older Japanese ANCA-associated vasculitis/RPGN patients [8]. Our case was elderly, so she was treated with intravenous methylprednisolone and oral PSL without cyclophosphamide. In our case, positivity of HBsAg and HBV-DNA was demonstrated after 6 weeks when corticosteroids were reduced to 3 mg from 5 mg. At this time, she did not have any other immunosuppressive or cytotoxic drugs, and she was diagnosed with DHN. Corticosteroids are widely used as a treatment for chronic kidney diseases, allergies, collagen disease, and autoimmune disorders, among others. Previously, corticosteroids were used to treat chronic hepatitis B, but in the 1980s, many studies concluded that such treatment produced no beneficial effects and that they caused HBV reactivation [9]. Kim et al. [10] reported the risk of HBV reactivation in HBsAg-positive patients with asthma or chronic obstructive pulmonary disease, who were treated with systemic corticosteroids, especially when systemic corticosteroids were administered chronically or at high doses. For renal disease, since immunosuppression can facilitate viral replication and lead to the exacerbation of hepatitis B, Tse et al. [11] indicated the importance of the serial monitoring of HBV DNA and transaminase levels, as well as prompt anti-viral therapy, in the management of HBsAg-positive lupus patients. However, in resolved cases, as in our case, HBV reactivation and DNH infrequently occur. The risk factors for HBV reactivation are known to include detectable HBsAg, HBV DNA, HBeAg, HBcAb, HBV genotype, younger age, and male sex [12]. In our case, we could not determine the HBV genotype, because HBV-DNA disappeared immediately after taking entecavir. The reactivation of HBV might be related to the degree of renal failure, and the using and tapering of corticosteroids.

Recently, some chimeric monoclonal antibodies were used for several diseases, and this single-use or combination chemotherapy with other drugs has been identified as a risk factor for HBV reactivation in HBsAg-negative patients, such as malignant lymphoma and rheumatic disease [2, 3]. More recently, chimeric monoclonal antibodies, such as rituximab and eculizumab, are beginning to be used in some renal diseases [1315]. Mansfield et al. [13] have documented the long-term efficacy and safety of a rituximab-based cyclophosphamide-sparing regimen for renal ANCA-associated vasculitis [13]. As shown in the current case report, DNH might occur even in patients given corticosteroids alone. Furthermore, currently, chimeric monoclonal antibodies are used in renal diseases more than ever and, therefore, there may be an increase in patients with DHN. For the management of HBV-infected patients and the prevention of HBV reactivation caused by immunosuppressive or cytotoxic therapy, some guidelines and proposed algorithms have been published [3, 16, 17]. Prior to the initiation of such immunosuppressive or cytotoxic therapy, these guidelines and algorithms recommend that screening be conducted in all cases for HBV-associated serological markers (HBsAg, HBcAb, and HBsAb) [16, 17]. Even in renal disease, to prevent the development of HBV reactivation caused by immunosuppressive or cytotoxic therapy, diagnosis regarding chronic HBV infection, as well as resolved HBV infection, needs to be carried out. Importance should be placed on the confirmation of levels of HBV propagation, even in resolved cases, by measurement of HBV DNA levels [16, 17]. Careful screening and monitoring of HBV appear to be the most rational approach for managing patients of renal disease, including MPO-ANCA-related nephritis, with previous HBV infection in patients who require immunosuppressive or cytotoxic therapy, including corticosteroids alone.

When HBV reactivation is diagnosed, it is mandatory to suspend all chemotherapy and start treatment with anti-viral agents immediately. Currently, five oral nucleotide antiviral drugs are approved for the treatment of chronic HBV infection: lamivudine, adefovir, entecavir, tenofovir, and telbivudine [18]. The most commonly used antiviral drug in HBV reactivation is lamivudine [1]. However, Tse et al. [11] reported five patients who had received lamivudine for hepatitis B in lupus nephritis, and 1 of 5 patients developed of lamivudine resistance. In our patient, entecavir was remarkably effective, providing rapid normalization of HBV reactivation. Antiviral treatment with entecavir was immediately initiated when the patient had HBV reactivation, and a rapid reduction of viral replication with normalization of transaminases was obtained. Entecavir, a new nucleoside analogue, is reported to induce few drug-resistant mutant viruses, unlike lamivudine, and, therefore, has replaced lamivudine [3, 16]. However, there is little evidence that entecavir is more favorable than lamivudine in the treatment of DNH [10]. Generally, entecavir is preferred because of its rapid onset of action and lack of nephrotoxicity. In addition, several reports have shown that the administration of entecavir is effective in the prevention of HBV reactivation [3, 16].

In conclusion, we describe a case of DNH in MPO-ANCA-related MPA treated with corticosteroids. HBV infection, especially resolved infection, is overlooked in renal diseases. To prevent HBV reactivation and DNH induced by immunosuppressive or cytotoxic therapy, including corticosteroids alone, the measurement of HBV-related serological markers needs to be performed prior to the initiation of such therapy, even in renal diseases.

Conflict of interest

None declared.

Copyright information

© Japanese Society of Nephrology 2012

Authors and Affiliations

  • Yoichi Iwafuchi
    • 1
  • Yuko Oyama
    • 1
  • Takashi Morita
    • 2
  • Akira Kamimura
    • 1
  • Shigeru Miyazaki
    • 3
  • Ichiei Narita
    • 4
  1. 1.Department of Internal MedicineKoseiren Sanjo General HospitalSanjoJapan
  2. 2.Department of PathologyShinrakuen HospitalNiigataJapan
  3. 3.Department of Internal Medicine, Kidney CenterShinrakuen HospitalNiigataJapan
  4. 4.Clinical Nephrology and Rheumatology, Department of Medicine IINiigata University Graduate School of Medical and Dental SciencesNiigataJapan