Hepatic adenomata with type 1 glycogen storage disease
- 27 September 1976
- journal article
- research article
- Published by American Medical Association (AMA) in JAMA
- Vol. 236 (13) , 1481-1484
- https://doi.org/10.1001/jama.236.13.1481
Abstract
In older patients with G-6-Pase deficiency, adenomatous nodules develop within the liver parenchyma. Investigation of 8 such patients, age 3-28 yr, using radioisotopic scans, demonstrated areas of depressed isotope uptake in the liver in all except the 1 preteenaged child. Three patients were further studied with hepatic angiograms and liver biopsy specimens. A diffuse nodularity, more widespread than apparent on isotopic scans, was demonstrated on angiograms. Although initial histologic study in each case showed adenomatous tissue without evidence of neoplasm, the development of hepatocellular carcinoma in 1 patient and in others from the literature suggests that the nodules may be premalignant.This publication has 2 references indexed in Scilit:
- Studies in Glycogen Storage Diseases. I. Intestinal Glucose-6-Phosphatase Activity in Patients with Von Gierke's Disease and Their Parents*Journal of Clinical Investigation, 1965
- Gout and Glycogen Storage DiseaseAnnals of Internal Medicine, 1963