Atypical presentations of autoimmune hepatitis (AIH)

Atypical presentations of autoimmune hepatitis (AIH)

Abstracts JOURNAL OF CLINICAL AND EXPERIMENTAL HEPATOLOGY 21st Annual Conference of Indian National Association for the Study of Liver (INASL), Marc...

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Abstracts

JOURNAL OF CLINICAL AND EXPERIMENTAL HEPATOLOGY

21st Annual Conference of Indian National Association for the Study of Liver (INASL), March 22–24, 2013 Hyderabad International Convention Centre, Hyderabad, India

AUTOIMMUNE HEPATITIS AND CHOLESTATIC LIVER DISEASE

Dinesh Jothimani, Olithselvan, J. Vargese, Vivekanandan, N. Gomathy, Rajasekhar, Srinivas, Cherian, Mohamed Rela Global Hospitals, Chennai, India

Case 1: A 49 year old lady presented with 4 months of jaundice, encephaolpathy, ascties and ankle oedema. Her blood results are shown in the Table 1. ANA was 1: 320, SMA negative, IgG 25.6 mg/dl. A CT abdomen showed contracted liver, moderate ascites and normal spleen. A liver biopsy showed AIH with collapse of reticulin plate, no cirrhosis.. This is a subacute liver failure due to AIH. Case 2: A 42 year old man had 2 days of fever, vomiting followed by jaundice. He became drowsy, and was shifted to our hospital. His blood tests are shown in Table 1. His Hepatitis E IgM was positive. Autoantibodies were negative. With conservative management his encephalopathy and biochemical parameters improved. Six weeks after his initial presentation bilirubin increased to 22.7 mg/dl with ALT 229, AST 313. A repeat autoantibody screen showed ANA 1:100. A liver biopsy showed lymphocytic portal tract inflammation, intracellular cholestasis with apoptosis. He was monitored for a month with rather worseining LFTs. This is acute liver failure due to Hepatitis E virus infection, triggering AIH. Case 3: A 41 year old lady developed poor appetite, jaundice and pruritus in 2009. Investigations elsewhere showed cholestastic jaundice. Her ANA 1:12560 and AMA 1:100.

Corresponding author. Dinesh Jothimani. E-mail: [email protected]

CHRONIC CHOLESTATIC DISORDERS (NON VIRAL, NON ALCOHOLIC): CLINICAL, BIOCHEMICAL, HISTOLOGICAL & RADIOLOGICAL PROFILE Ghulam NabiYattoo, Shah Ahtisham, Showkat Ali Zargar, GulJavid, Yasin Mujoo, Shaheen Parveen, Shaheen Nazir Department of Gastroenterology, SKIMS Soura, Srinagar, India

Background and Objectives: Chronic intrahepatic cholestasis includes disorders of the hepatic ductal system of varied etiologies; autoimmune, genetic, infiltrative, drugs etc. The spectrum of these disorders has not been reported

Table 1 Case 1

Case 2

Case 3

October 2012

December 2012

August 2012

Jan 2013

Sep 2012

Dec2012

AST

128

29

2921

138

63

21

ALT

77

38

4000

164

51

18

Bilirubin

18.6

0.67

21

10.6

1.8

1.6

Albumin

1.6

2.7

3.3

2.6

3

3

INR

2.8

1.4

4.4

1.1

1.07

1.0

ALP

82

93

321 (normal 130)

290 (normal 280)

GGT

36

82

362

300

© 2013, INASL

Journal of Clinical and Experimental Hepatology | March 2013 | Vol. 3 | No. 1S | S33–S36

Autoimmune Hepatitis and Cholestatic Liver Disease

ATYPICAL PRESENTATIONS OF AUTOIMMUNE HEPATITIS (AIH)

Follwing a liver biospy steroids, azathioprine and ursodeoxycholic acid was commenced. However the former 2 drugs were stopped because of osteoporotic fracture left foot and leucopenia, respectively. A repeat liver biopsy in 2012 showed cirrhosis due to PBC & AIH overlap syndrome. She was referred to our hospital for further management. Her blood tests are outlined in the table. Review of biopsy confirmed above findings.All these patients received corticosteroids with good improvement in clinical condition. Conclusion: AIH presentation may vary substantially as described above. AIH should be borne in mind when the clinical scenario not fully explained by a single disease.