[Auto-immune hepatitis in chronic granulomatous disease in a 2-year-old girl].. Hépatite auto-immune associée à une granulomatose septique chronique chez une fille de 2 ans

Archive ouverte

Gargouri, L. | Safi, F. | Mejdoub, I. | Maalej, B. | Mekki, N. | Mnif, H. | Ben Mustapha, I. | Barbouche, Mohamed-Ridha | Boudawara, T. | Mahfoudh, A.

Edité par CCSD ; Elsevier -

International audience. Background. Chronic granulomatous disease is a rare inherited primary immune deficiency disease characterized by recurrent infection and an increased susceptibility to autoimmunity disorders. We report on the case of a girl with autoimmune hepatitis in chronic granulomatous disease to describe the clinical and biological features and treatment implications for patients with chronic granulomatous disease associated with autoimmune disorders. Case report. An 18-month-old girl was referred to our department for investigation of hepatomegaly. She was the third child of non-consanguineous parents. Her two elder sisters had died from infectious diseases at an early age. She had elevated liver transaminase levels with a normal gamma globulin concentration. Negative results were found for all autoimmune markers (antinuclear antibody, anti-smooth muscle, anti-liver-kidney microsomal, anti-liver cytosol and anti-soluble liver antigen). Her liver biopsy showed features of interface hepatitis with portal fibrosis. The diagnosis of seronegative autoimmune hepatitis was established. Treatment with corticosteroids and azathioprine led to clinical improvement with normalization of transaminases. Six months after initial presentation, at the age of 2 years, she was readmitted for fever. Staphylococcus aureus bacteremia was identified with multiple foci of infection (skin infection, arthritis of the right elbow, pneumonia, buttock abscess). The immunological workup revealed chronic granulomatous disease. The course was marked by a fatal outcome despite appropriate antibiotics and intensive care. Conclusion. Early diagnosis of the association between chronic granulomatous disease and autoimmune disorders allows for appropriate treatments, improves the quality of life for affected patients, and reduces the risk of mortality. (C) 2015 Elsevier Masson SAS. All rights reserved.

Consulter en ligne

Suggestions

Du même auteur

[Serratia marcescens osteomyelitis as the first manifestation of chronic granulomatous disease].. Granulomatose septique chronique révélée par une ostéomyélite à Serratia marcescens

Archive ouverte | Ben Abdallah Chabchoub, R. | CCSD

International audience. Chronic granulomatous disease is a rare, primary immunodeficiency disorder characterized by a defect in oxidative metabolism in phagocytes and recurrent bacterial and fungal infections. We re...

[Listeriosis in Tunis: seven cases reports].

Archive ouverte | Elbeldi, A. | CCSD

International audience. Listeria monocytogenesis a Gram positive facultative intracellular bacterium that can be responsible for severe infections, affecting essentially pregnant women, immunocompromised patients at...

Rare splicing defects of FAS underly severe recessive autoimmune lymphoproliferative syndrome.

Archive ouverte | Agrebi, N. | CCSD

International audience. Autoimmune lymphoproliferative syndrome (ALPS) is a prototypic disorder of impaired apoptosis characterized by autoimmune features and lymphoproliferation. Heterozygous germline or somatic FA...

Chargement des enrichissements...