| Volumen 20 números 1 y 2 - 2023 | 
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            ISSN 0718-0918  | 
           
          
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            | Tabla de Contenidos > Caso Clínico | 
           
          
            HALLAZGO INCIDENTAL LUEGO DE UN TRAUMA ABDOMINAL: CARCINOMA  HEPATOCELULAR FIBROLAMELAR REPORTE DE CASO EN UN PACIENTE PEDIÁTRICO 
Natalia Peñaloza Barrios1, Marcela Osorio Santos2 Sharon Romero  Vergara3, María Camila Arévalo Pérez1, Carolina María Díaz Guerra1,  Heidy María Marsiglia Armella1 2, Andrea Carolina Zárate Vergara4,  Irina Suley Tirado Pérez5 
1 Servicio de  Hemato Oncología Pediátrica, Hospital Infantil Napoleón Franco Pareja (CTG, CO) 
2 Especialización  en Pediatría, Facultad de Medicina, Universidad de Cartagena (CTG, CO) 
3 Especialización  en Pediatría, Facultad de Ciencias de la Salud, Universidad de Libre (BAQ, CO) 
4 Especialista en  cuidado intensivo pediátrico, Clínica especializada la Concepción (SJO, CO) 
5 Médica epidemióloga, Máster cuidado paliativo  pediátrico, Especialización en Pediatría, Facultad de Ciencias de la Salud,  Corporación Universitaria Remington (CUR), (MED, CO) 
 
Resumen |Abstract | Texto completo | Descargar cuerpo en pdf  | 
           
          
            Introduction: Primary malignant tumors of the liver are  extremely rare. It represents only 1% of all malignancies in the pediatric age  group, with less than 1.5 cases per million children under 18 years of age.  Hepatoblastoma is the most common primary hepatic neoplasm (48%);  Hepatocellular carcinoma is the second most common primary liver neoplasm in  childhood (27%), and the rest are vascular tumors and sarcomas. The type of  fibrolamellar hepatocellular carcinoma is rare, usually seen in the older age  group (median age 26 ,4 years).  
              Clinical case: The case report is made since there are few  cases reported in the literature, it is an 11-year-old patient who suffers  trauma to the abdomen due to a fall on a bicycle, which is why she consults,  draws attention with no previous history, totally asymptomatic, but with  increased hepatomegaly and abdominal pain during hospitalization, for which  extension studies were performed, with evidence by contrast magnetic resonance,  of a tumor lesion that involved the entire right hepatic lobe with confirmation  by biopsy of a fibrolamellar variant.  
              Conclusion: Liver tumors are infrequent, the  fibrolamellar variant is even more unusual, the typical age of presentation is  young adults, for which its presentation in pediatric age is very scarce;  Initially, its management is based on surgical resection, depending on the  stage presented at the time of diagnosis. 
              Key words: Fibrolamellar hepatocellular carcinoma, hepatocellular carcinoma,  carcinoma, hepatic neoplasia, pediatric  | 
           
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