Sood Apurva, Singh Harpreet, Sood Ashwani, Basher Rajender Kumar, Mittal Bhagwant Rai
Department of Nuclear Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Indian J Nucl Med. 2017 Jul-Sep;32(3):224-226. doi: 10.4103/ijnm.IJNM_37_17.
Peptide receptor radionuclide therapy (PRRT) either using Lu-177 or Y-90 peptide radiopharmaceuticals has emerged as promising treatment modality in patients with inoperable metastatic neuroendocrine tumour (NET) including medullary thyroid cancer, because of overexpression of somatostatin receptor 2 (sstr-2) on these cells. The several investigators have used PRRT in non-iodine avid differentiated thyroid cancer patients with limited success, where other treatment modalities have failed, probably due to faint sstr-2 expression in these lesions. However Hurthle cell neoplasms being predominantly non-iodine avid lesions have shown sstr-2 over-expression. The present case of inoperable NET patient imaged and treated with radiolabelled somatostatin analogue showed incidentally detected thyroid lesion highlighting the its importance in imaging and treatment in these type of thyroid malignancies.
使用镥-177或钇-90肽放射性药物的肽受体放射性核素治疗(PRRT)已成为无法手术的转移性神经内分泌肿瘤(NET)患者(包括甲状腺髓样癌)的一种有前景的治疗方式,因为这些细胞上生长抑素受体2(sstr-2)的过度表达。几位研究者在其他治疗方式失败的非碘亲和性分化型甲状腺癌患者中使用PRRT,但成功率有限,这可能是由于这些病变中sstr-2表达微弱。然而,许特耳细胞肿瘤主要是非碘亲和性病变,已显示出sstr-2的过度表达。本例无法手术的NET患者用放射性标记的生长抑素类似物进行成像和治疗,偶然发现了甲状腺病变,突出了其在这类甲状腺恶性肿瘤成像和治疗中的重要性。