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Hepatocellular Carcinoma of Fibrolamellar Type in an Adolescent: Case Report and Literature Review.

Authors :
Santiago-Reynoso J
Zamaripa-Martínez KS
Dorantes-Loya JM
Gaytán-Fernández GJ
Apolinar-Jiménez E
Paz-Gómez F
Farias-Serratos F
Maldonado-Vega M
Source :
Gastrointestinal tumors [Gastrointest Tumors] 2019 Aug; Vol. 6 (1-2), pp. 43-50. Date of Electronic Publication: 2019 May 27.
Publication Year :
2019

Abstract

We present a female patient, 13 years old, with diagnosis of hepatocellular carcinoma of fibrolamellar type, which was rapidly evolving. The fibrolamellar hepatocellular carcinoma invaded more than 80% of the hepatic parenchyma without surgical possibility or liver transplantation. Measures applied corresponded to chemotherapy of 1 cycle of cisplatin 40 mg/s/5 days + vincristine 1.5 mg/m <superscript>2</superscript> /day, 5-fluorouracil, doxorubicin, and dexrazoxane. The case presented aggressive evolution of hepatocellular carcinoma, which led to acute liver failure, with hyperammonemia, sepsis, pulmonary focus plus septic shock, grade III-IV encephalopathy, portal hypertension, and ascites with intra-abdominal hypertension. Death occurred due to multiple organ failure, which involved respiratory failure type KDIGO 1 and 2, acute liver failure, severe pneumonia, pericardial effusion, AKIN 2 acute kidney injury, carcinoma, and pulmonary metastasis. This type of ailment is infrequent in children and adolescents, and the first symptoms are crucial to achieve treatment possibilities.<br />Competing Interests: The authors have no conflicts of interest to declare.<br /> (Copyright © 2019 by S. Karger AG, Basel.)

Details

Language :
English
ISSN :
2296-3774
Volume :
6
Issue :
1-2
Database :
MEDLINE
Journal :
Gastrointestinal tumors
Publication Type :
Report
Accession number :
31602376
Full Text :
https://doi.org/10.1159/000499581