We report on two cases of type I glycogen storage disease (GSD) complicated by malignant tumors. A 23-year-old man had GSD Ia with adenomatosis. He underwent transplantation for rapidly growing and radiologically changing adenomata. At histological examination, one adenoma had become a hepatocellular carcinoma. A 22-year-old, HBV-infected woman had GSD type Ib with adenomatosis. At follow-up, several tumors showed changing morphological characteristics. Pre-transplant laparotomy confirmed the presence of a metastatic cholangiocarcinoma. Liver transplantation should be considered in GSD type I patients with adenomatosis, especially when tumor characteristics change. Regular detailed Doppler ultrasound and magnetic nuclear resonance screening...
Type III glycogen storage disease (GSD) is a disorder of carbohydrate metabolism caused by a deficie...
Glycogen storage disease type I (GSD I) is a metabolic disorder resulting from defects in the glucos...
Glycogen storage disease type la (GSD la) is a rare metabolic disorder due to hepatic glucose-6-phos...
Glycogen storage diseases (GSD) are inherited metabolic disorders of glycogen metabolism due to intr...
The aim of this study was to collect data from patients who underwent liver transplantation (LT) for...
Glycogen storage disease (GSD) types I, III, and IV can be associated with severe liver disease. The...
The aim of this study was to collect data from patients who underwent liver transplantation (LT) for...
International audienceThe aim of this study was to collect data from patients who underwent liver tr...
Glycogen storage disease type Ia (GSDIa) is an inherited disorder of glucose metabolism, due to the ...
Background: Glycogenosis type I (von Gierke's disease) is an inherited hepatic glycogen storage dise...
INTRODUCTION: Glycogen storage disease type Ia (GSDIa) is due to the deficiency of glucose-6-phospha...
Type III glycogen storage disease (GSD) is a disorder of carbohydrate metabolism caused by a deficie...
The development of hepatocellular adenomas and – more rarely – carcinoma in the liver of patients wi...
Type 1a glycogen storage disease (GSD 1a), or von Gierke disease, is a rare, autosomal-recessive dis...
Glycogen storage disease type I (GSDI), an inborn error of carbohydrate metabolism, is caused by def...
Type III glycogen storage disease (GSD) is a disorder of carbohydrate metabolism caused by a deficie...
Glycogen storage disease type I (GSD I) is a metabolic disorder resulting from defects in the glucos...
Glycogen storage disease type la (GSD la) is a rare metabolic disorder due to hepatic glucose-6-phos...
Glycogen storage diseases (GSD) are inherited metabolic disorders of glycogen metabolism due to intr...
The aim of this study was to collect data from patients who underwent liver transplantation (LT) for...
Glycogen storage disease (GSD) types I, III, and IV can be associated with severe liver disease. The...
The aim of this study was to collect data from patients who underwent liver transplantation (LT) for...
International audienceThe aim of this study was to collect data from patients who underwent liver tr...
Glycogen storage disease type Ia (GSDIa) is an inherited disorder of glucose metabolism, due to the ...
Background: Glycogenosis type I (von Gierke's disease) is an inherited hepatic glycogen storage dise...
INTRODUCTION: Glycogen storage disease type Ia (GSDIa) is due to the deficiency of glucose-6-phospha...
Type III glycogen storage disease (GSD) is a disorder of carbohydrate metabolism caused by a deficie...
The development of hepatocellular adenomas and – more rarely – carcinoma in the liver of patients wi...
Type 1a glycogen storage disease (GSD 1a), or von Gierke disease, is a rare, autosomal-recessive dis...
Glycogen storage disease type I (GSDI), an inborn error of carbohydrate metabolism, is caused by def...
Type III glycogen storage disease (GSD) is a disorder of carbohydrate metabolism caused by a deficie...
Glycogen storage disease type I (GSD I) is a metabolic disorder resulting from defects in the glucos...
Glycogen storage disease type la (GSD la) is a rare metabolic disorder due to hepatic glucose-6-phos...