Abstract
Chromaffin tumors are defined as neoplasias composed of catecholamine-producing, -storing, and -secreting cells. They therefore develop not only in the adrenal medulla but also in sympathetic paraganglia. Regardless of their intra- or extra-adrenal localization, we shall use the term pheochromocytoma for all expansive growing forms of these tumors and the term pheochromoblastoma for all infiltrating and metastasizing forms (Table 1; Käser 1985). However, it must be emphasized that even the nonmalignant pheochromocytoma must be considered as lifethreatening disease. In fact, its endocrine activity may lead to death if the tumor remains unrecognized and untreated. However, if correctly diagnosed, this neural crest tumor can be removed by surgery, and most patients can thus be cured.
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Käser, H. (1990). Clinical and Diagnostic Findings in Patients with Chromaffin Tumors: Pheochromocytomas, Pheochromoblastomas. In: Beck, L., Grundmann, E., Ackermann, R., Röher, HD. (eds) Hormone-Related Malignant Tumors. Recent Results in Cancer Research, vol 118. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-83816-3_10
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DOI: https://doi.org/10.1007/978-3-642-83816-3_10
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