Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA.
Endocr Relat Cancer. 2012 Feb 13;19(1):83-93. doi: 10.1530/ERC-11-0243. Print 2012 Feb.
The purpose of this study was to present the characteristics and outcome of patients with proven pheochromocytoma or paraganglioma who had false-negative iodine-123 metaiodobenzylguanidine single photon emission computed tomography ((123)I-MIBG SPECT). Twenty-one patients with false-negative (123)I-MIBG SPECT (7 males, 14 females), aged 13-55 years (mean: 41.40 years), were included. We classified them as nonmetastatic or metastatic according to the stage of the disease at the time of false-negative (123)I-MIBG SPECT study, the location and size of the tumor, plasma and urinary catecholamine and metanephrine levels, genetic mutations, and outcome in terms of occurrence and progression of metastases and death. Thirteen patients were evaluated for metastatic tumors, while the remaining eight were seen for nonmetastatic disease. All primary tumors and multiple metastatic foci did not show avid (123)I-MIBG uptake regardless of the tumor diameter. The majority of patients had extraadrenal tumors with hypersecretion of normetanephrine or norepinephrine. SDHB mutations were present in 52% (n=11) of cases, RET mutation in 4% (n=1), and the rest were apparently sporadic. Twenty-four percent (n=5) had metastatic disease on initial presentation. Fourteen patients were followed for 3-7 years. Of them, 71% (n=10) had metastatic disease and the majority had SDHB mutations. Nine are still alive, while five (four with SDHB) died due to metastatic disease. We concluded that false-negative (123)I-MIBG SPECT is frequently related to metastatic tumors and usually due to SDHB mutations with unfavorable prognosis. We therefore recommend that patients with false-negative (123)I-MIBG SPECT be tested for SDHB mutations and undergo more regular and close follow-up.
本研究旨在介绍碘-123 间碘苄胍单光子发射计算机断层扫描(123I-MIBG SPECT)假阴性的嗜铬细胞瘤或副神经节瘤患者的特征和结局。21 例 123I-MIBG SPECT 假阴性患者(7 名男性,14 名女性),年龄 13-55 岁(平均:41.40 岁),纳入本研究。根据 123I-MIBG SPECT 假阴性时的疾病分期、肿瘤位置和大小、血浆和尿儿茶酚胺和甲氧基肾上腺素水平、基因突变以及转移和死亡的发生和进展情况,我们将其分为非转移性或转移性。13 例患者评估了转移性肿瘤,其余 8 例患者为非转移性疾病。所有原发性肿瘤和多个转移性病灶均未显示浓聚(123)I-MIBG 摄取,无论肿瘤直径大小如何。大多数患者有嗜铬细胞瘤,表现为去甲肾上腺素或去甲变肾上腺素的过度分泌。SDHB 突变见于 52%(n=11)的病例,RET 突变见于 4%(n=1),其余病例为散发性。24%(n=5)在初次就诊时就有转移性疾病。14 例患者随访 3-7 年。其中,71%(n=10)有转移性疾病,大多数有 SDHB 突变。9 例仍存活,5 例(4 例伴有 SDHB)因转移性疾病死亡。我们得出结论,假阴性(123)I-MIBG SPECT 常与转移性肿瘤有关,通常与 SDHB 突变有关,预后不良。因此,我们建议对假阴性(123)I-MIBG SPECT 患者进行 SDHB 突变检测,并进行更定期和密切的随访。