TY - JOUR
T1 - Malignant pheochromocytoma
T2 - A review
AU - Harari, Avital
AU - Inabnet, William B.
PY - 2011/5
Y1 - 2011/5
N2 - Background: Pheochromocytomas are rare catecholamine-secreting tumors. Approximately 10 percent of pheochromocytomas are malignant. Traditionally, there has been no reliable method available to predict the malignant potential of pheochromocytoma. However, recent research has increased focus on differentiating at the time of surgery/diagnosis those pheochromocytoma tumors which have malignant potential. In this review, we discuss the current information known of malignant pheochromocytomas. Data sources: The PubMed database was searched for articles on malignant pheochromocytoma published between 1993 and 2010. Conclusions: The difficult task of predicting the malignant potential of a pheochromocytoma has yet to be answered definitively. However, all the studies presented give an idea of what we may look for in these tumors at the time of diagnosis. We have provided an algorithm based on the most current information known. A much larger study should be performed to test many of these theories with enough power to determine a standard of care.
AB - Background: Pheochromocytomas are rare catecholamine-secreting tumors. Approximately 10 percent of pheochromocytomas are malignant. Traditionally, there has been no reliable method available to predict the malignant potential of pheochromocytoma. However, recent research has increased focus on differentiating at the time of surgery/diagnosis those pheochromocytoma tumors which have malignant potential. In this review, we discuss the current information known of malignant pheochromocytomas. Data sources: The PubMed database was searched for articles on malignant pheochromocytoma published between 1993 and 2010. Conclusions: The difficult task of predicting the malignant potential of a pheochromocytoma has yet to be answered definitively. However, all the studies presented give an idea of what we may look for in these tumors at the time of diagnosis. We have provided an algorithm based on the most current information known. A much larger study should be performed to test many of these theories with enough power to determine a standard of care.
KW - Endocrinology
KW - Malignant
KW - Oncology
KW - Paraganglioma
KW - Pheochromocytoma
KW - Review
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U2 - 10.1016/j.amjsurg.2010.04.012
DO - 10.1016/j.amjsurg.2010.04.012
M3 - Review article
C2 - 20870212
AN - SCOPUS:79955678783
SN - 0002-9610
VL - 201
SP - 700
EP - 708
JO - American Journal of Surgery
JF - American Journal of Surgery
IS - 5
ER -