{"title":"免疫性血小板减少性紫癜:甲型肝炎合并急性肝衰竭的罕见表现","authors":"Pranab Kumar Dey, Eshita Das, Nairit De","doi":"10.18502/ijpho.v13i4.13774","DOIUrl":null,"url":null,"abstract":"
 
 
 
 
 
 
 
 
 
 
 Hepatitis A Virus (HAV) infection is a benign, self-limited gastrointestinal infection of children. Autoimmune hematological manifestation is very rare in children. Here, we report an 11-year-old male child having HAV infection with acute liver failure, complicated with persistent thrombocytopenia and haematuria during the course of illness and eventually diagnosed as a case of HAV infection associated with immune thrombocytopenic purpura. The child was treated successfully with a short course of steroid therapy.
 
 
 
 
 
 
 
 
 
 
 
 
 
","PeriodicalId":44212,"journal":{"name":"Iranian Journal of Pediatric Hematology and Oncology","volume":null,"pages":null},"PeriodicalIF":0.4000,"publicationDate":"2023-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Immune Thrombocytopenic Purpura: An uncommon manifestation of Hepatitis A with acute liver failure\",\"authors\":\"Pranab Kumar Dey, Eshita Das, Nairit De\",\"doi\":\"10.18502/ijpho.v13i4.13774\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"
 
 
 
 
 
 
 
 
 
 
 Hepatitis A Virus (HAV) infection is a benign, self-limited gastrointestinal infection of children. Autoimmune hematological manifestation is very rare in children. Here, we report an 11-year-old male child having HAV infection with acute liver failure, complicated with persistent thrombocytopenia and haematuria during the course of illness and eventually diagnosed as a case of HAV infection associated with immune thrombocytopenic purpura. The child was treated successfully with a short course of steroid therapy.
 
 
 
 
 
 
 
 
 
 
 
 
 
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Immune Thrombocytopenic Purpura: An uncommon manifestation of Hepatitis A with acute liver failure
Hepatitis A Virus (HAV) infection is a benign, self-limited gastrointestinal infection of children. Autoimmune hematological manifestation is very rare in children. Here, we report an 11-year-old male child having HAV infection with acute liver failure, complicated with persistent thrombocytopenia and haematuria during the course of illness and eventually diagnosed as a case of HAV infection associated with immune thrombocytopenic purpura. The child was treated successfully with a short course of steroid therapy.