A clinicopathologic study of primary hepatic carcinoid tumors
Open Access
- 1 March 1990
- Vol. 65 (5) , 1211-1218
- https://doi.org/10.1002/1097-0142(19900301)65:5<1211::aid-cncr2820650530>3.0.co;2-m
Abstract
Six cases of primary hepatic carcinoid tumors were studied with combined immunocytochemical and electron microscopic techniques. Positive tumor immunostaining with PHE5, LK2H10, neuron‐specific enolase (NSE), serotonin, gastrin, and insulin antibodies was observed. At the ultrastructural level, cytoplasmic dense granules were seen in all the cases tested. This finding supports a putative origin of these carcinoids found in the liver from a pluripotential stem cell. The clinical course and follow‐up of these cases suggests that this unusual hepatic neoplasm has a more favorable prognosis than other forms of hepatic cancer.This publication has 13 references indexed in Scilit:
- Endocrine liver tumour differential diagnosis from hepatocellular carcinomaHistopathology, 1985
- Significance of intestinal metaplasia for the evolution of cancer in the biliary tractCancer, 1984
- Hepatocellular carcinoma with carcinoid featuresHuman Pathology, 1984
- Ulrastructure of Liver Cell and Bile Duct CarcinomasUltrastructural Pathology, 1983
- Ectopic ACTH Syndrome in APUD TumorsOncology, 1982
- Pancreatic-polypeptide-producing apudoma of the liverCancer, 1980
- Malignant apudoma of the liver with symptomatic intractable hypoglycemiaCancer, 1978
- CholangiocarcinomaA clinicopathologic study of five cases with ultrastructural observationsHuman Pathology, 1974
- Hepatocellular carcinoma with the carcinoid syndromeCancer, 1971
- Three Cases Illustrating the Presence of Argentaffin (Kultschitzky) Cells in the Human Gall-bladderJournal of Clinical Pathology, 1954