TY - JOUR
T1 - [123I]metaiodobenzylguanidine and [111In]octreotide uptake in benign and malignant pheochromocytomas
AU - Van Der Harst, Erwin
AU - De Herder, Wouter W.
AU - Bruining, Hajo A.
AU - Bonjer, H. Jaap
AU - De Krijger, Ronald R.
AU - Lamberts, Steven W.J.
AU - Van De Meiracker, Anton H.
AU - Boomsma, Frans
AU - Stijnen, Theo
AU - Krenning, Eric P.
AU - Bosman, Fred T.
AU - Kwekkeboom, Dik J.
PY - 2001
Y1 - 2001
N2 - Selecting the appropriate approach for resection and follow-up of pheochromocytomas (PCCs) is highly dependent upon reliable localization and exclusion of multifocal, bilateral, or metastatic disease. Metaiodobenzylguanidine (MIBG) scintigraphy was developed for functional localization of catecholamine-secreting tissues. Somatostatin receptor imaging (SRI) has a high sensitivity for localizing head and neck paragangliomas, but studies of intraabdominal PCCs are rare. In this study we review our experience of [123I]MIBG and SRI, performed since 1983 and 1989, respectively, in the work-up of primary and recurrent PCCs. Scintigraphic results were correlated with catecholamine secretion, size and site, malignancy, associated tumor syndromes, and morphological features. [123I]MIBG scans were performed in a total of 75 patients, in 70 cases before resection of primary PCCs and in 5 cases because of recurrent disease. Ninety-one PCCs were resected. The overall detection rates were 83.3% and 89.8% for PCCs larger than 1.0 cm. Multifocal disease was detected in 4 patients with [123I]MIBG. [123I]MIBG uptake correlated with greater size of PCC (r = 0.33; P = 0.008) and greater concentration of plasma epinephrine (r = 0.32; P = 0.006). [123I]MIBG-negative PCCs (n = 14) had significantly (P = 0.01) smaller diameters than [123I]MIBG-positive tumors. Furthermore, [123I]MIBG uptake was significantly higher in unilateral (P = 0.02), benign (P = 0.02), sporadic (P = 0.02), intraadrenal (P = 0.02), and capsular invasive (P = 0.03) PCCs than in bilateral, malignant, MEN2A/2B-related, extraadrenal, and noninvasive PCCs, respectively. The detection rate of SRI was only 25% (8 of 32) for primary benign PCCs. In 14 patients metastases occurred, which were effectively visualized with [123I]MIBG in 8 of 14 cases. SRI was able to detect metastases in 7 of 8 cases, including 3 [123I]MIBG-negative metastatic cases. In addition, [123I]MIBG and SRI detected 2 recurrences. In conclusion, [123I]MIBG uptake is correlated with the size, epinephrine production, and site of PCCs. Its role in bilateral and MEN2A/2B-related PCCs seems limited. In cases of recurrent elevation of catecholamines, localization of metastases and/or recurrence should be attempted with [123I]MIBG scintigraphy. In suspicious metastatic PCCs, SRI might be considered to supplement [123I]MIBG scintigraphy.
AB - Selecting the appropriate approach for resection and follow-up of pheochromocytomas (PCCs) is highly dependent upon reliable localization and exclusion of multifocal, bilateral, or metastatic disease. Metaiodobenzylguanidine (MIBG) scintigraphy was developed for functional localization of catecholamine-secreting tissues. Somatostatin receptor imaging (SRI) has a high sensitivity for localizing head and neck paragangliomas, but studies of intraabdominal PCCs are rare. In this study we review our experience of [123I]MIBG and SRI, performed since 1983 and 1989, respectively, in the work-up of primary and recurrent PCCs. Scintigraphic results were correlated with catecholamine secretion, size and site, malignancy, associated tumor syndromes, and morphological features. [123I]MIBG scans were performed in a total of 75 patients, in 70 cases before resection of primary PCCs and in 5 cases because of recurrent disease. Ninety-one PCCs were resected. The overall detection rates were 83.3% and 89.8% for PCCs larger than 1.0 cm. Multifocal disease was detected in 4 patients with [123I]MIBG. [123I]MIBG uptake correlated with greater size of PCC (r = 0.33; P = 0.008) and greater concentration of plasma epinephrine (r = 0.32; P = 0.006). [123I]MIBG-negative PCCs (n = 14) had significantly (P = 0.01) smaller diameters than [123I]MIBG-positive tumors. Furthermore, [123I]MIBG uptake was significantly higher in unilateral (P = 0.02), benign (P = 0.02), sporadic (P = 0.02), intraadrenal (P = 0.02), and capsular invasive (P = 0.03) PCCs than in bilateral, malignant, MEN2A/2B-related, extraadrenal, and noninvasive PCCs, respectively. The detection rate of SRI was only 25% (8 of 32) for primary benign PCCs. In 14 patients metastases occurred, which were effectively visualized with [123I]MIBG in 8 of 14 cases. SRI was able to detect metastases in 7 of 8 cases, including 3 [123I]MIBG-negative metastatic cases. In addition, [123I]MIBG and SRI detected 2 recurrences. In conclusion, [123I]MIBG uptake is correlated with the size, epinephrine production, and site of PCCs. Its role in bilateral and MEN2A/2B-related PCCs seems limited. In cases of recurrent elevation of catecholamines, localization of metastases and/or recurrence should be attempted with [123I]MIBG scintigraphy. In suspicious metastatic PCCs, SRI might be considered to supplement [123I]MIBG scintigraphy.
UR - http://www.scopus.com/inward/record.url?scp=0037896855&partnerID=8YFLogxK
U2 - 10.1210/jc.86.2.685
DO - 10.1210/jc.86.2.685
M3 - Article
C2 - 11158032
AN - SCOPUS:0037896855
SN - 0021-972X
VL - 86
SP - 685
EP - 693
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 2
ER -