Michałowska Ilona, Ćwikła Jarosław B, Pęczkowska Mariola, Furmanek Mariusz I, Buscombe John R, Michalski Wojciech, Prejbisz Aleksander, Szperl Małgorzata, Malinoc Angelica, Moczulski Dariusz, Szutkowski Zbigniew, Kawecki Andrzej, Antoniewicz Jolanta, Pęczkowski Piotr, Lewczuk Anna, Otto Maciej, Cichocki Andrzej, Bednarek-Tupikowska Grażyna, Kabat Marek, Janaszek-Sitkowska Hanna, Przybyłowska Katarzyna, Janas Jadwiga, Neumann Hartmut P H, Januszewicz Andrzej
Department of Radiology, Institute of Cardiology, Warsaw, Poland.
Neuroendocrinology. 2015;101(4):321-30. doi: 10.1159/000381458. Epub 2015 Mar 13.
The aim of this study was to assess the usefulness of somatostatin receptor scintigraphy (SRS) using (99m)Tc-[HYNIC, Tyr3]-octreotide (TOC) and 123I-metaiodobenzylguanidine (mIBG) in patients with SDHx-related syndromes in which paragangliomas were detected by computed tomography and to establish an optimal imaging diagnostic algorithm in SDHx mutation carriers.
All carriers with clinical and radiological findings suggesting paragangliomas were screened by SRS and 123I-mIBG. Lesions were classified by body regions, i.e. head and neck, chest, abdomen with pelvis and adrenal gland as well as metastasis.
We evaluated 46 SDHx gene mutation carriers (32 index cases and 14 relatives; 28 SDHD, 16 SDHB and 2 SDHC). In this group, 102 benign tumors were found in 39 studied patients, and malignant disease was diagnosed in 7 patients. In benign tumors, the sensitivity of SRS was estimated at 77% and of 123I-mIBG at 22.0%. The SRS and mIBG sensitivity was found to be clearly region dependent (p < 0.001). The highest SRS sensitivity was found in head and neck paragangliomas (HNP; 91.4%) and the lowest was found in abdominal paragangliomas and pheochromocytomas (40 and 42.9%, respectively). The highest 123I-mIBG sensitivity was found in pheochromocytomas (sensitivity of 100%) and the lowest in HNP (sensitivity of 3.7%). In metastatic disease, SRS was superior to mIBG (sensitivity of 95.2 vs. 23.8%, respectively).
SRS and 123I-mIBG single photon emission computed tomography (SPECT) sensitivity in SDHx patients is highly body region dependent. In malignant tumors, SRS is superior to 123I-mIBG SPECT.
本研究旨在评估使用(99m)Tc-[HYNIC,Tyr3]-奥曲肽(TOC)和123I-间碘苄胍(mIBG)的生长抑素受体闪烁显像(SRS)在通过计算机断层扫描检测到副神经节瘤的SDHx相关综合征患者中的实用性,并在SDHx突变携带者中建立最佳的成像诊断算法。
所有具有提示副神经节瘤的临床和影像学表现的携带者均通过SRS和123I-mIBG进行筛查。病变按身体部位分类,即头颈部、胸部、腹部及盆腔和肾上腺以及转移情况。
我们评估了46名SDHx基因突变携带者(32例索引病例和14名亲属;28例SDHD、16例SDHB和2例SDHC)。在该组中,39名研究患者共发现102个良性肿瘤,7名患者被诊断为恶性疾病。在良性肿瘤中,SRS的敏感性估计为77%,123I-mIBG的敏感性为22.0%。发现SRS和mIBG的敏感性明显依赖于身体部位(p<0.001)。SRS敏感性最高的是头颈部副神经节瘤(HNP;91.4%),最低的是腹部副神经节瘤和嗜铬细胞瘤(分别为40%和42.9%)。123I-mIBG敏感性最高的是嗜铬细胞瘤(敏感性为100%),最低的是HNP(敏感性为3.7%)。在转移性疾病中,SRS优于mIBG(敏感性分别为95.2%和23.8%)。
SDHx患者中SRS和123I-mIBG单光子发射计算机断层扫描(SPECT)的敏感性高度依赖于身体部位。在恶性肿瘤中,SRS优于123I-mIBG SPECT。