Article
Pheochromocytoma: A Clinicopathologic and Molecular Study of 390 Cases From a Single Center.
The American journal of surgical pathology - 1 Sept 2021
Liu Zhonghua, Ma Junsheng, Jimenez Camilo, Zhang Miao
Abstract excerpt
Pheochromocytomas are rare neuroendocrine tumors arising from chromaffin cells in the adrenal medulla. They may occur sporadically or in the context of hereditary syndromes. All pheochromocytomas are considered to have malignant potential (defined as risk of metastasis, not local invasion). The use of grading systems with incorporated clinical and histopathologic parameters can help but not definitively predict...
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