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Pheochromocytomas and Ganglioneuromas in the Aging Rats: Morphological and Immunohistochemical CharacterizationNovartis Pharma AG, Preclinical Safety, Toxicology/Pathology, Basle, Switzerland, virgilio.pace{at}dompe.it
Novartis Pharma AG, Preclinical Safety, Toxicology/Pathology, Basle, Switzerland
Novartis Pharma AG, Preclinical Safety, Toxicology/Pathology, Basle, Switzerland We investigated, morphologically and immunohistochemically, 74 medullary adrenal tumors, including 64 pheochromocytomas (14 malignant and 50 benign), 9 ganglioneuromas, and 1 malignant schwannoma. The tumors were detected in 2-year-old Wistar and Sprague—Dawley rats from carcinogenicity studies. Morphologically, benign pheochromocytomas were characterized by monomorphic, small, basophilic cells with almost absence of mitoses. Malignant pheochromocytomas presented a low grade of pleomorphism, higher rate of mitoses, necrosis, infiltrative growth and in 1 case metastases in the lung. Ganglioneuromas were characterized by ganglion and neuron-like cells embedded in an eosinophilic matrix containing neurites, Schwann cells, and scant fibrovascular elements. All pheochromocytomas were strongly immunoreactive for tyrosine hydroxylase (TH), the rate-limiting enzyme in catecholamine synthesis. Subpopulations of chromaffin cells expressed chromogranin A (CGA) positivity. Matrix and Schwann cells were positive for S-100 and for glial fibrillary acidic protein (GFAP). In focal areas of the tumors, ganglion cells and axons were positive for neurofilament proteins (NFP) and synaptophysin. Ganglion cells exhibited peripherin and ß-tubulin. Proliferative activity of the tumors was assessed by immunostaining the endogenous cell proliferation associated-antigen Ki-67 and the proliferating cell nuclear antigen (PCNA). As expected, cell proliferation indeces were much higher in malignant pheochromocytomas than in benign, yet ganglioneuromas remained immunonegative. Considering that Ki-67 antigen is more specific for cell proliferation, it should be regarded as marker of choice for supporting the differential diagnosis between benign and malignant pheochromocytomas.
Key Words: Pheochromocytomas • ganglioneuromas • rats • Ki-67 • peripherin • ß-tubulin • proliferating cell nuclear antigen (PCNA) • adrenal gland.
Toxicologic Pathology, Vol. 30, No. 4,
492-500 (2002) This article has been cited by other articles:
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