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HAV Infection Associated with Hemophagocytic Syndrome

Aamri, H. ; Elqadiry, R. ; Nassih, H. ; Bourrahouat, A. ; Ait Sab, I. Marangoni, Antonella ; Antonella Marangoni

Case reports in infectious diseases, 2023-01, Vol.2023, p.7799252-2 [Periódico revisado por pares]

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Título:
HAV Infection Associated with Hemophagocytic Syndrome
Autor: Aamri, H. ; Elqadiry, R. ; Nassih, H. ; Bourrahouat, A. ; Ait Sab, I.
Marangoni, Antonella ; Antonella Marangoni
Assuntos: Asymptomatic ; Blood ; Bone marrow ; Case Report ; Case reports ; Cytokines ; Cytomegalovirus ; Epstein-Barr virus ; Fever ; Hematology ; Hemoglobin ; Hepatitis A ; HIV ; Human immunodeficiency virus ; Immune system ; Immunoglobulins ; Infections ; Laboratories ; Lymphatic system ; Lymphocytes ; Patients ; Pediatrics ; Steroids ; Triglycerides ; Viral infections
É parte de: Case reports in infectious diseases, 2023-01, Vol.2023, p.7799252-2
Notas: Academic Editor: Antonella Marangoni
Descrição: Hemophagocytic syndrome is a rare disease that can cause severe illness and death. This condition is caused by the presence of antibodies against the hepatitis A virus. A positive anti-IGM antibody was identified in our 7-year-old patient with severe hepatitis A. A week after the hepatitis A was diagnosed, the patient experienced pancytopenia, which was worsened by prolonged fever. He was then diagnosed with macrophage activation syndrome. The treatment with steroids improved the clinical and biological evolution of the condition.
Editor: Egypt: Hindawi
Idioma: Inglês

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