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Fibrolamellar Carcinoma: A Rare Liver Neoplasm
Elily D Apumayta1, Aaron Kahlam2, Eloy F Ruiz2
1Department of Abdominal Surgery, Instituto Nacional de Enfermedades Neoplasicas, Lima, PER.
Fibrolamellar carcinoma, a rare liver tumor, often affects young adults. This case series highlights that liver resection is a primary treatment, but recurrence is common, with 60% of patients experiencing it within a year.
Area of Science:
- Hepatology
- Oncology
- Surgical Pathology
Background:
- Fibrolamellar carcinoma (FLC) is a rare subtype of hepatocellular carcinoma.
- FLC predominantly affects adolescents and young adults without underlying liver disease.
- Diagnosis often occurs incidentally due to nonspecific symptoms.
Observation:
- A case series of five patients with histologically confirmed FLC is presented.
- The median age at diagnosis was 24 years.
- Patients presented with nonspecific symptoms, normal health, and variable alpha-fetoprotein levels.
Findings:
- All patients underwent liver resection, primarily hemihepatectomy.
- Classical imaging, macroscopic, and microscopic features were observed.
- A high recurrence rate of 60% was noted within the first year post-resection.
Implications:
- Liver resection is a key treatment for FLC.
- The high recurrence rate underscores the need for vigilant surveillance and novel therapeutic strategies.
- Further research into FLC pathogenesis and management is warranted.
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