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Probl Endokrinol (Mosk) ; 67(5): 58-66, 2021 10 03.
Article in Russian | MEDLINE | ID: mdl-34766492

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.


Subject(s)
Craniopharyngioma , Hepatopulmonary Syndrome , Non-alcoholic Fatty Liver Disease , Pituitary Neoplasms , Craniopharyngioma/complications , Craniopharyngioma/surgery , Female , Hepatopulmonary Syndrome/complications , Hepatopulmonary Syndrome/surgery , Humans , Liver Cirrhosis/complications , Liver Cirrhosis/surgery , Non-alcoholic Fatty Liver Disease/complications , Non-alcoholic Fatty Liver Disease/surgery , Obesity/complications , Pituitary Neoplasms/complications , Pituitary Neoplasms/surgery
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