focal nodular hyperplasia/carbohydrate

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Hepatocellular carcinoma and focal nodular hyperplasia of the liver in a glycogen storage disease patient.

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Glycogen storage disease type Ia (GSD-Ia; also called von Gierke disease) is an autosomal recessive disorder of carbohydrate metabolism caused by glucose-6-phosphatase deficiency. There have been many reports describing hepatic tumors in GSD patients; however, most of these reports were of

Hepatic angiomyolipoma: clinical, imaging and pathological features in 178 cases.

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The aim of the study was to review the main clinical, imaging and pathological features of hepatic angiomyolipoma (HAML). We retrospectively analyzed the imaging, pathological and clinical features of 178 patients who underwent surgical resection for HAML. Forty-three males and 135 females with a

Perioperative management of benign hepatic tumors in patients with glycogen storage disease type Ia.

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Glycogen storage disease type Ia (GSD-Ia; von Gierke disease) is an inherited disorder caused by glucose-6-phosphatase deficiency, and there have been some reports of hepatic tumors in patients with this disease. We report two patients with benign hepatic tumors with GSD-Ia. One is a 19-year-old man

Evaluation of tumour markers as differential diagnostic tool in patients with suspicion of liver metastases from breast cancer.

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OBJECTIVE The liver is the site of breast cancer metastasis in 50% of patients with advanced disease. Tumour markers have been demonstrated as being useful in follow-up of patients with breast cancer, in early detection of recurrence of breast cancer after radical surgical treatments, and in

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