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间碘苄胍(MIBG)扫描未能检测出患有琥珀酸脱氢酶B(SDHB)基因突变的小儿转移性嗜铬细胞瘤的转移灶。

Failure of MIBG scan to detect metastases in SDHB-mutated pediatric metastatic pheochromocytoma.

作者信息

Sait Sameer, Pandit-Taskar Neeta, Modak Shakeel

机构信息

Department of Pediatrics, Memorial Sloan Kettering Cancer Centre, New York, New York.

Departments of Pediatrics and Radiology, Memorial Sloan Kettering Cancer Centre, New York, New York.

出版信息

Pediatr Blood Cancer. 2017 Nov;64(11). doi: 10.1002/pbc.26549. Epub 2017 Apr 14.

Abstract

I-meta-iodo benzyl guanidine (MIBG) scans are considered the gold standard imaging in neuroblastoma; however, flouro deoxy glucose positron emission tomography (FDG-PET) scans have increased sensitivity in adults with pheochromocytoma/paraganglioma. We describe a pediatric patient initially considered to have localized neuroblastoma based on anatomical imaging and I-MIBG scan, but subsequent investigations revealed germline succinate dehydrogenase complex iron sulfur subunit B (SDHB) mutation-associated pheochromocytoma with multiple FDG-avid skeletal metastases. We then compared I-MIBG and FDG-PET scans in children with metastatic pheochromocytoma/paraganglioma. FDG-PET was superior to I-MIBG scan for the detection of skeletal metastases (median number of skeletal lesions detected 10 [range 1-30] vs. 2 [range 1-26], respectively; P = 0.005 by t-test). FDG-PET should be considered the functional scan of choice in children with pheochromocytoma/paraganglioma.

摘要

间碘苄胍(MIBG)扫描被认为是神经母细胞瘤的金标准成像;然而,氟代脱氧葡萄糖正电子发射断层扫描(FDG-PET)扫描对成人嗜铬细胞瘤/副神经节瘤的敏感性更高。我们描述了一名儿科患者,最初根据解剖成像和I-MIBG扫描被认为患有局限性神经母细胞瘤,但随后的检查发现其患有与种系琥珀酸脱氢酶复合物铁硫亚基B(SDHB)突变相关的嗜铬细胞瘤,并伴有多处FDG摄取的骨转移。然后,我们比较了转移性嗜铬细胞瘤/副神经节瘤患儿的I-MIBG和FDG-PET扫描。FDG-PET在检测骨转移方面优于I-MIBG扫描(检测到的骨病变中位数分别为10[范围1-30]和2[范围1-26];经t检验,P=0.005)。FDG-PET应被视为嗜铬细胞瘤/副神经节瘤患儿的首选功能扫描。

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