Introduction

Autoimmune hepatitis (AIH) was first reported in the 1950s by Jan Waldenstrom in a group of young women with persistent transaminitis [1]. AIH is a progressive inflammatory liver disease of unknown aetiology that is commoner in females [2]. It is characterized biochemically by elevated transaminases and serum immunoglobulin G (IgG), serologically by non-organic specific and liver specific autoantibodies and histologically by interface hepatitis [3]. The age of onset ranges from infancy to eighth decade of life. However, it is quite uncommon before the age of 2 years, and the incidence is higher between 10 and 30 years [4]. The diagnosis is made after other known causes of liver disease have been excluded and typically there is response to immune suppression [3]. There is associated 40% of family history and 20% of personal history of other autoimmune diseases like thyroiditis, coeliac disease, inflammatory bowel disease, vitiligo, insulin dependent diabetes mellitus and nephrotic syndrome either at presentation or at follow up [5, 6].

There are 2 types of AIH depending on the type of antibodies isolated in serology: antinuclear antibody (ANA) and/or smooth muscle antibody (SMA) in type 1 AIH, and in type 2 there is liver kidney microsomal antibody (anti-LKM) or antibody to liver cytosolic antigen type1 (LC1) [7]. In children, lower autoantibodies levels are considered as positive. For example, ANA and SMA levels of ≥ 1:20 and anti-LKM of ≥ 1:10 are positive whilst higher levels of ≥1: 40 are considered positive in adults [4]. Like other autoimmune diseases, AIH is increasing in prevalence over the years. In the United Kingdom, a 6-fold yearly increase was reported over the period between 1990 to the 2000s [8] whilst in Canada, an incidence rate of 0.23 cases per 100,000 children was noted [9]. Not much is known about AIH in African children. To the best of our knowledge only Egypt has two published data in Africa [10, 11] on paediatric AIH. The first study concerned 30 cases from the year 2000 to 2008 [10] and the second, 25 cases [11] over a 13-year period between 2004 and 2017. Both studies had female predominance with type 1 AIH diagnosed in all cases. All patients in both studies had varying degrees of liver disease. Presentations of AIH in children are similar to that seen in adults. Clinical features of AIH vary and can mimic any form of liver disease from fulminant hepatitis to chronic liver disease with features of cirrhosis and portal hypertension [12]. Treatment is predominantly with prednisolone with or without azathioprine [13]. In paediatric AIH, remission is defined as complete clinical recovery with transaminase levels within the normal range, normalization of IgG levels, negative or very low-titre autoantibodies, and histological resolution of inflammation and this depends on the disease severity at presentation [8]. Our study highlights the clinical profile of paediatric AIH cases at a referral hospital in Ghana.

Materials and methods

Results

Demography and clinical features

Thirteen patients with a median age of 10 years (range, 5 to 13 years) and majority females 8(61.5%) were diagnosed with autoimmune liver disease most of whom were autoimmune hepatitis (Table 1). These patients were being followed up for four and half years to eleven months with a median of two years five months.

Table 1

Clinical features and types of autoimmune diseases.

Characteristics (n = 13 patients)	Frequencies
Age at presentation in years (median [range])	10 (5–13)
Duration of symptoms (median in months)	5
Gender, n (%)
Male	5 (38.5)
Female	8 (61.5)
Clinical presentation, n (%)
Fulminant	1 (7.7)
Acute	2 (15.7)
Insidious	10 (76.6)
Complications of chronic liver disease	8 (61.5)
Detailed clinical findings, n (%)
Jaundice	13 (100)
Weight loss	6 (46.2)
Bleeding	3 (23.1)
Anasarca	4 (30.8)
Hepatomegaly	8 (61.5)
Splenomegaly	6 (46.2)
Ascites	5 (38.5)
Encephalopathy	2 (15.4)
Auto-immune disorders, n (%)
Auto-immune hepatitis (all Type 1)	11 (84.6)
Autoimmune sclerosing cholangitis	2 (15.4)
Systemic lupus erythematosus	1 (7.7)
Ulcerative colitis	1 (7.7)

Clinical and laboratory features

Tables 1–3 below show the clinical features, disease outcome and the laboratory investigations done respectively. The duration of symptoms in most but one patient with fulminant hepatitis was between 5 to 24 months with an average of 10 months. The patient with fulminant hepatitis had a duration of symptoms of 1 week and he tested negative for both hepatitis A and E infections. Most patients had chronic liver disease and portal hypertension, with eight patients presenting with hypoalbuminaemia, four with thrombocytopaenia, 8 with anaemia, two with anasarca and three with oesophageal varices, symptomatic with bleeding episodes. The varices were treated with endoscopic variceal band ligation. Histology was done in 9 (69.2%) patients whilst the rest had to start treatment without histology due to severe coagulopathy or advanced liver disease (Fig 1).

Fig 1

Histology of autoimmune hepatitis showing interphase hepatitis with periportal inflammation dominated by lymphocytes.

Table 2

Baseline full blood count, liver function test and INR results at presentation.

Patients	Hb (g/dL)	Platelets (x106/L)	WBC (x106/L)	INR	Albumin (g/L)	Total Protein (g/L)	ALP (U/L)	ALT (U/L)	AST (U/L)	GGT (IU/L)	Total bilirubin (μmol/L)	Direct bilirubin (μmol/L)
1	10.7	151	2.9	5.1	28	100	577	249	449	118	234	209
2	9.4	228	7.2	1.7	41	92	639	1526	1819	116	315	253
3	7.4	113	3.8	8.2	33	67	452	279	345	58	284	242
4	9.1	73	4.6	5.1	19	58	396	155	179	55	251	179
5	11.7	360	7.3	1.4	41	81	434	1175	1090	128	277	138
6	11.6	428	6.5	5.9	31	55	241	722	1567	40	551	246
7	8.3	650	4.8	4.8	21	76	932	473	356	116	376	247
8	9.8	112	3.6	3.7	28	78	442	531	556	116	219	186
9	12.6	453	5.8	1.1	43	88	455	864	543	89	244	202
10	13.1	306	5.3	4.8	34	75	794	3175	2025	77	285.2	132
11	9.9	180	11.4	1.4	35	84	381	270.9	246.9	265	186.7	113
12	9.0	342	7.1	0.9	41	91	873	326	234	96	115	103
13	9.4	137	4.2	3.9	27	65	227	26	69	75	550	408

ALP: alkaline phosphatase; ALT: alanine aminotransferase; AST: aspartate aminotransferase; GGT: gamma glutamyl transferase; Hb: haemoglobin; INR: international normalised ratio; WBC: white blood cells

Table 3

Serology and haemoglobin electrophoresis results at presentation.

Patients	ANA	SMA	Anti LKM-1	IgG(6.5–16.0g/L)	HBsAg	Anti-HCV	HCV PCR	Schistosoma IgM	HIV ½	Hb electrophoresis
1	Neg	1:80	Neg	26.40	Neg	Neg		Pos	Neg	AS
2	1:80	1:40	Neg	22.62	Neg	Pos	Neg		Neg	SS
3	Neg	1:40	Neg	18.64	Neg	Neg			Neg	AA
4	1:20	1:20	Neg	20.60	Neg	Neg		Pos	Neg	AA
5	Neg	1:20	Neg	18.20	Neg	Neg			Neg	AS
6	Neg	1:20	Neg	20.42	Neg	Neg		Pos	Neg	AA
7	1:20	1:40	Neg	17.80	Neg	Neg			Neg	AA
8	Neg	Neg	Neg	18. 94	Neg	Neg			Neg	AA
9	Neg	1:80	Neg	21.10	Neg	Neg			Neg	AS
10	Neg	1:80	Neg	12.22	Neg	Neg			Neg	AA
11	Neg	Neg	Neg	18.80	Neg	Neg			Neg	AA
12	1:80	Neg	Neg	21.50	Neg	Neg			Neg	AA
13	Neg	1:20	Neg	12.53	Neg	Neg			Neg	AA

ANA: antinuclear antibodies; AntiLKM-1: anti liver kidney microsomal type 1; Anti-HCV: hepatitis C antibodies; HCV: hepatitis C virus; HBsAg: hepatitis B surface antigen; Hb: haemoglobin; HIV: human immunodeficiency virus; IgG: immunoglobulin G; IgM: immunoglobulin M; Neg: negative; Pos: positive

Four patients had other types of autoimmune disorders. Two patients had autoimmune sclerosing cholangitis or overlap syndrome, after an initial diagnosis of AIH. These patients developed cholestasis during treatment for which Magnetic Resonance Cholangiopancreatography (MRCP) and liver biopsy were done to confirm the diagnosis. One patient had ulcerative colitis, and another had systemic lupus erythematosus making the total of 2 patients with other personal history of non-hepatic autoimmune disorders. There was no family history of autoimmune diseases in these patients. All patients tested negative for Wilson’s disease, hepatitis B and HIV. Three patients had specific IgM for Schistosoma mansoni and were treated with two courses of praziquantel prior to the diagnosis of AIH. Schistosoma specific Ig M were lost during AIH-specific treatment, as autoantibody levels have normalized.

Discussion

This is the first report on paediatric AIH from Ghana and possibly from sub Saharan Africa This study, similarly to those from Egypt, did not find any asymptomatic patient as it is usually seen in developed countries [4]. Many odds are against these cohorts with AIH. These are that, autoimmune liver disease in children is inherently aggressive and progresses rapidly with complications [14]. In African Americans, who share a common ancestry with these cohorts, AIH is usually diagnosed at advanced stage with cirrhosis but with good response to therapy [15]. Females predominance of eight (61.5%) patients in this study is similar to that reported in the two Egyptian studies, with 60% [11] and 70.5% [10] respectively and one Canadian study with 60.3% [9]. None of the patients in this study had Type 2 AIH. Type 2 AIH is less common (10%) in paediatric AIH [16] and is usually seen in a small population of younger children [3]. Most of the patients 10 (76.6%) presented insidiously as they had been seen at peripheral health facilities for months without a diagnosis.

We excluded Retroviral infection (HIV) [17], sickle cell disease [18], Schistosomiasis [19] as possible causes of liver disease in our patients because of high prevalence of these conditions in African countries. False positive viral antibodies had been reported in up to 11% of patients with AIH [20]. The positive report of both the hepatitis C virus and Schistosomiasis antibodies in this study may be due to molecular mimicry confounded my hypergammaglobulinaemia in AIH [21]. The finding of two (15.4%) of these cohorts with normal Ig G level is similar to that reported in international literature where 15% of patients with type 1 AIH had normal Ig G level and are usually with acute presentation [22]. The frequency of other concurrent autoimmune diseases such as ulcerative colitis and systemic lupus erythematosus in this study is similar to the prevalence reported in other studies [23]. The commonest reported extra hepatic autoimmune diseases include, thyroid disease, autoimmune skin diseases, coeliac disease and inflammatory bowel disease [23]. This indicate that all children with autoimmune liver disease should be screened for other autoimmune diseases annually [23].

Liver biopsy and histology required for confirmation and staging of the disease, was done in only nine (69.2%) because of advance liver disease at presentation complicated with coagulopathy, bleeding and ascites, which are contraindications for liver biopsy. In our facility where transjugular liver biopsy is not available, these patients with other laboratory features of AIH were treated with good response similar to what was done in adult studies [24]. All the patients had good response to the standard treatment with prednisolone with or without azathioprine, regardless of the severity of the liver disease [4]. Except for the 2 patients who died, all the remaining patients are still on treatment and are doing well. The circumstances of the mortalities recorded highlight the difficulties in managing patients in developing countries. There is thus, the need for public awareness creation about liver diseases, the importance of seeking healthcare early and remain in care throughout the duration of treatment.

Conclusion

Autoimmune liver disease is also presented in indigenous African children. It should be investigated for in all children with liver disease of any severity, as it is a very treatable condition. Diseases like sickle cell disease and HIV should always be excluded in populations with high prevalence of these diseases. Furthermore, early diagnosis and therapy would reduce liver-related complications.