Idiopathic adulthood ductopenia with elevated transaminase only: A case report

Xiao-Chen Zhang, Di Wang, Xiang Li, Yu-Lin Hu, Chong Wang

Xiao-Chen Zhang, Di Wang, Xiang Li, Yu-Lin Hu, Chong Wang, Department of Hepatology, The First Hospital of Jilin University, Changchun 130021, Jilin Province, China

Abstract BACKGROUND Idiopathic adulthood ductopenia (IAD) is a chronic cholestatic liver disease of unknown etiology that usually presents as unexplained jaundice. It is characterized by adult onset, lack of autoantibodies, inflammatory bowel disease and loss of interlobular bile ducts.CASE SUMMARY This case presents a 27-year-old woman with elevation of transaminases and alkaline phosphatase without clinical symptoms. Five years ago, the patient had abnormal transaminases but no cholestasis. Three months before admission,physical examination revealed an increase in transaminases. Oral hepatoprotective drugs did not show any significant improvement, and she was admitted to hospital for further diagnosis and treatment. Liver biopsy confirmed IAD. After about 2 wk of ursodeoxycholic acid treatment, serological and histological examination showed a significant response.CONCLUSION IAD is a manifestation of cholestasis, but also may be an abnormal increase in transaminase in the early stage.

Key Words: Idiopathic adulthood ductopenia; Ductopenic diseases; Liver injury;Cholestasis; Ursodeoxycholic acid; Case report

INTRODUCTION

Idiopathic adulthood ductopenia (IAD) is a rare chronic liver disease that is often misdiagnosed. IAD was first described in 1988 by Ludwiget al[1], with interlobular bile ducts disappearing without a clear origin[2]. So far, less than 100 cases have been reported[3]. In recent years, the pathology and pathogenesis of bile duct loss have been widely studied, and a number of hepatobiliary diseases have been added to the list of ductopenic diseases[4]. IAD is a special type of ductopenic disease that is characterized by adult onset, autoantibodies negative, inflammatory bowel disease and absence of interlobular bile ducts[5].

This report presents a case that had no obvious clinical symptoms. The patient was diagnosed with IAD and was treated with ursodeoxycholic acid (UDCA).

CASE PRESENTATION

Chief complaints

A 27-year-old female was hospitalized for continuous elevation of transaminases and alkaline phosphatase without clinical symptoms or signs.

History of present illness

The patient had abnormally elevated transaminases at physical examination 5 years ago, but this was not concerning to her. The patient found abnormal transaminases again at physical examination 2 years ago, and was admitted to the hospital. After admission, the patient was tested for ceruloplasmin, which was negative. The patient had no viral hepatitis markers, and autoantibodies were absent. The patient was discharged from the hospital when her liver function improved after hepatoprotective treatment. In the past 2 years, liver function was rechecked three times, and it was still abnormal. Liver function test results 3 mo before the present admission were:Aspartate transaminase (AST) 213.8 U/L (0-40 U/L), alanine transaminase (ALT) 321.8 U/L (0-40 U/L), alkaline phosphatase (ALP) 317 U/L (15-112 U/L) and γglutamyltransferase (GGT) 172.1 U/L (7-32 U/L). After oral bicyclol treatment (25 mg/d), liver function was rechecked 8 d before admission, showing the following results: AST 251 U/L (13-35 U/L), ALT 419 U/L (7-40 U/L), ALP 337 U/L (35-100 U/L) and GGT 232 U/L (7-45 U/L). There were no improvements, so the patient was admitted to the hospital again.

History of past illness

The patient had taken oral Chinese medicine to treat folliculitis 3 years ago.

Personal and family history

The patient did not have any family history.

Physical examination

The liver area was sensitive to light palpation, and there were no obvious positive signs.

Laboratory examinations

Her liver function results were as follows: AST 169.5 U/L, ALT 261.5 U/L, ALP 231.6 U/L and GGT 167.7 U/L; erythrocyte sedimentation rate: 24 mm/h (2-20 mm/h); five items of immunity: Immunoglobulin G 21.50 g/L (6-16 g/L), complement C3 1.47 g/L(0.7-1.28 g/L) and antinuclear antibody normal. There were no abnormalities in hepatitis B and C markers,Treponema pallidumantibody, anti-human immunodeficiency virus antibody, antimitochondrial antibody M2 and tumor markers.

Imaging examinations

Multi-row computed tomography of the liver, gallbladder, spleen and pancreas demonstrated diffuse fatty liver or chronic liver injury.

Further diagnostic work-up

After 5 d of hepatoprotective treatment, the liver function was rechecked, with AST 130.4 U/L, ALT 84.8 U/L, ALP 236.9 U/L and GGT 194.4 U/L. AST and ALT decreased significantly, but ALP and GGT did not improve significantly. After that,liver biopsy was performed, and the pathological results suggested the following: (1)Local I with balloon-like degeneration of hepatocytes, mild expansion and fibrosis in some portal areas, infiltration of plasma cells and a few lymphocytes in the stroma. (2)Part of the inherent bile duct disappeared (＞ 50%), degeneration of the bile duct and mild hyperplasia of the thin bile duct (Figure 1). It was recommended to exclude vanishing bile duct syndrome. Pathological results at Beijing Youan Hospital were: (1)Vanishing bile duct syndrome; (2) More plasma cell infiltration and focal interfacial inflammation in portal areas; and (3) Lobular hepatitis in the recovery period that may have been related to recent medication.

FINAL DIAGNOSIS

IAD.

TREATMENT

The patient was given UDCA (250 mg twice daily) after admission.

OUTCOME AND FOLLOW-UP

Re-examination of liver function after 2 wk of treatment showed that AST and ALT had returned to normal, and ALP was 146.1 U/L and GGT 114.8 U/L. According to the pathological results, the treatment was considered effective.

DISCUSSION

This patient was a young female without a clear cause of IAD. A retrospective medical history revealed that there were abnormal transaminases 5 years ago, but no cholestasis. There were no obvious clinical symptoms, but only mild percussion pain in the liver area. Imaging examinations after admission suggested chronic liver injury.The abnormal liver function was mainly due to elevated a-fetoprotein and GGT accompanied by mild cholestasis, so autoimmune liver disease was considered.Related laboratory tests excluded the possibility of autoimmune hepatitis and primary biliary cholangitis. Although the patient had a history of oral Chinese medicine, liver function tests showed abnormal transaminases before taking the medicine, so it is unlikely that IAD was caused by drug-induced liver injury. Therefore, the diagnosis depended on liver biopsy. The patient had a normal extrahepatic biliary tract and had no evidence of inflammatory bowel disease. A liver biopsy specimen presented loss of interlobular bile ducts from ＞ 50% of the portal area. Combined with liver histological features, a diagnosis of IAD was made.

Figure 1 Pathology and immunohistochemical staining. A-C: Liver pathology staining showing plasma cell infiltration and focal interfacial inflammation in the confluence area and mild interfacial inflammation; D: Immunohistochemical staining of cytokeratin 7 showing that most of the intrahepatic bile ducts were missing(＞ 50%).

The diagnostic criteria for IAD include the following: (1) The patient must be an adult or at least an adolescent; (2) Biopsy ought to show a reduction in intrahepatic bile ducts in at least 50% of the portal areas; and (3) There should be no identifiable causes of cholestasis[1]. As for therapy, related research has shown that some patients have improvement in liver function tests with UDCA[6]. Since the patient was admitted to hospital, she has been treated with UDCA. Liver biopsy can establish whether UDCA is effective for treatment of IAD. However, for patients with rapid disease progression, UDCA does not improve the condition, and they will ultimately require liver transplantation[7]. Cirrhosis caused by IAD has been reported in some cases, and its progression is faster than other types of cirrhosis[8].

CONCLUSION

IAD is a manifestation of cholestasis, but also may be an abnormal increase in transaminase in the early stage. For liver injury of unknown cause, when we exclude primary biliary cholangitis, autoimmune hepatitis and drug-induced liver injury, liver biopsy can be performed to clarify the diagnosis. For patients who have been diagnosed, long-term UDCA treatment should be used to reduce liver cell damage and help with liver cell repair and bile duct regeneration and reconstruction. UDCA has a positive effect on the long-term prognosis of the disease. Further examinations are still necessary to evaluate the recovery of bile ducts and arrest the disease progress in a timely manner.