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[Hepatopulmonary syndrome: a rare manifestation of cirrhosis in patient with diencephalic obesity and nonalcoholic fatty liver disease after surgery for craniopharyngioma].

Authors :
Mazerkina NA
Savateev AN
Gorelyshev SK
Mariashev SA
Beregovskaya SA
Konovalov AN
Source :
Problemy endokrinologii [Probl Endokrinol (Mosk)] 2021 Oct 03; Vol. 67 (5), pp. 58-66. Date of Electronic Publication: 2021 Oct 03.
Publication Year :
2021

Abstract

We describe a 15-year girl, who developed panhypopituitarism and diencephalic obesity after surgical excision of craniopharyngioma, followed by nonalcoholic fatty liver disease and cirrhosis 5 years after surgery. Cirrhosis in this case manifested by hypoxia due to hepatopulmonary syndrome, and despite cure of craniopharyngioma by surgery and radiosurgery treatment and adequate hormonal substitution therapy patient died 9 years after surgery. Growth hormone substitutional therapy in patients with hypopituitarism, and steatohepatitis may decrease liver triglyceride accumulation and prevent end-stage liver disease.

Details

Language :
Russian
ISSN :
2308-1430
Volume :
67
Issue :
5
Database :
MEDLINE
Journal :
Problemy endokrinologii
Publication Type :
Academic Journal
Accession number :
34766492
Full Text :
https://doi.org/10.14341/probl12723