{"title":"Regenerative Nodule as a Diagnostic Dilemma in the Neonate With Acute Liver Failure and a Focal Liver Lesion.","authors":"Claire Castaneda, Jessica Gulliver, Katryn Furuya, Shelly Cook, Eumenia Castro, Crystal Bockoven, Sarangarajan Ranganathan","doi":"10.1177/10935266261427176","DOIUrl":null,"url":null,"abstract":"<p><p>Acute liver failure in the neonate generates a broad differential diagnosis of varying etiology including inborn errors of metabolism, infections, cholestatic disorders, gestational alloimmune liver disease (GALD), alpha-1 antitrypsin deficiency, total parenteral nutrition-related injury, malignancy, and others. We present a case of a neonate born at 39 weeks' gestational age who presented on day 5 of life with coxsackievirus (part of the enterovirus family) encephalitis and COVID-19 infection and was subsequently found to be in acute liver failure (INR 1.7 up to 2.8 [not correctable with parenteral vitamin K], ammonia 87 umol/L up to 142 umol/L, AST 1864 IU/L, ALT 535 IU/L) with increasing alpha-fetoprotein. Evaluation for possible liver transplantation included an abdominal MRI, which showed a 2.4 × 1.7 × 2.1 cm round mass-like lesion in segment 2 of the liver, raising a differential diagnosis which included hepatoblastoma. This lesion and the background liver were biopsied. A nonspecific hepatitic pattern of injury was identified within the lesion and the background liver showed nodular post-necrotic changes with collapse of lobular architecture. While clinical case reports exist of acute hepatitis in neonates with COVID-19 alone and coxsackievirus alone, the role dual infection may play in causing severe liver injury is unique to our case and provides territory for continued investigation.</p>","PeriodicalId":520743,"journal":{"name":"Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society","volume":" ","pages":"561-565"},"PeriodicalIF":1.3000,"publicationDate":"2026-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/10935266261427176","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/3/19 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Acute liver failure in the neonate generates a broad differential diagnosis of varying etiology including inborn errors of metabolism, infections, cholestatic disorders, gestational alloimmune liver disease (GALD), alpha-1 antitrypsin deficiency, total parenteral nutrition-related injury, malignancy, and others. We present a case of a neonate born at 39 weeks' gestational age who presented on day 5 of life with coxsackievirus (part of the enterovirus family) encephalitis and COVID-19 infection and was subsequently found to be in acute liver failure (INR 1.7 up to 2.8 [not correctable with parenteral vitamin K], ammonia 87 umol/L up to 142 umol/L, AST 1864 IU/L, ALT 535 IU/L) with increasing alpha-fetoprotein. Evaluation for possible liver transplantation included an abdominal MRI, which showed a 2.4 × 1.7 × 2.1 cm round mass-like lesion in segment 2 of the liver, raising a differential diagnosis which included hepatoblastoma. This lesion and the background liver were biopsied. A nonspecific hepatitic pattern of injury was identified within the lesion and the background liver showed nodular post-necrotic changes with collapse of lobular architecture. While clinical case reports exist of acute hepatitis in neonates with COVID-19 alone and coxsackievirus alone, the role dual infection may play in causing severe liver injury is unique to our case and provides territory for continued investigation.