肾上腺肿瘤的放射性核素显像诊断。

W H Beierwaltes, J C Sisson, B Shapiro
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引用次数: 0

摘要

1969年,放射性标记胆固醇作为肾上腺皮质类固醇生产的前体的发展,使肾上腺皮质的第一次无创成像成为可能。FDA-NDA于1984年批准,允许在大多数医院常规使用这些药物。NP-59最常用于库欣综合征的诊断和治疗;第二常用的是原发性醛固酮增多症的诊断。它也有助于肾上腺和卵巢雄激素分泌过多和多毛症的鉴别诊断,并且是检测单侧肾上腺皮质功能减退的唯一无创方法。最新和最流行的应用是在CT扫描中偶然发现的肾上腺区域无症状肿块(“偶发瘤”)的鉴别诊断。在这种情况下,NP-59扫描可以确定肿瘤是否在肾上腺以及它是功能性的还是非功能性的。我们相信,在未来,放射性标记酶抑制剂可能提供更好的肾上腺皮质诊断成像,尽管这些药物可能在一段时间内无法常规使用。我们开发的放射性碘化胍乙啶类似物131I-MIBG,可以在高血压或心动过速、血浆或尿儿茶酚胺增加或异常CT扫描出现之前,将正常肾上腺髓质功能与双侧肾上腺髓质增生区分开来。寻找嗜铬细胞瘤应从131I-MIBG显像开始。虽然超过90%的原发性嗜铬细胞瘤发生在腹部,但腹部的检查或单个肿瘤的发现都不应结束研究。CT扫描只能发现肿块,而MIBG扫描不仅能发现肿块,还能证明肿块是否为嗜铬细胞瘤。在所有其他局部研究正常的情况下,我们发现了小的或复发性的pheos。目前的药物和x线治疗在治疗肾上腺髓质转移性癌方面相对无效。5例患者的初步结果首次表明,一种复杂的有机分子可以在治疗有效剂量的照射下可重复地携带131I进入肾上腺肿瘤。我们也可以选择哪些患者对治疗剂量的131I-MIBG有反应,哪些患者没有反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnosis of adrenal tumors with radionuclide imaging.

The development of radiolabeled cholesterols in 1969 as precursors of adrenocortical steroid production allowed the first noninvasive imaging of the adrenal cortices. FDA-NDA approval in 1984 should allow routine use of these agents in most hospitals. NP-59 is most commonly used in the diagnosis and management of Cushing syndrome; the second most common use is in the diagnosis of primary aldosteronism. It is also helpful in the differential diagnosis of adrenal and ovarian hyperandrogenism and hirsutism, and is the only noninvasive method of detecting unilateral adrenocortical hypofunction. The newest and most popular use is in the differential diagnosis of asymptomatic masses in the region of the adrenal gland discovered incidentally with CT scan ("incidentalomas"). In this situation, the NP-59 scan can define whether the tumor is in the adrenal gland and if it is functional or nonfunctional. We believe that, in the future, radiolabeled enzyme inhibitors might offer better diagnostic imaging of the adrenal cortex, although these agents will probably not be available for routine use for some time. Our development of a radioiodinated guanethidine analog, 131I-MIBG, has allowed differentiation of normal adrenal medullary function from bilateral adrenal medullary hyperplasia before the development of hypertension or tachycardia, diagnostic increases in plasma or urinary catecholamines, or abnormal CT scans. The search for a pheochromocytoma should begin with 131I-MIBG scintigraphy. While over 90% of primary pheochromocytomas occur in the abdomen, neither a survey of the abdomen nor the finding of a single tumor should conclude the search. Whereas the CT scan can only detect a mass, the MIBG scan not only detects the mass but proves whether the mass is a pheochromocytoma. We have detected small or recurrent pheos when all other localizing studies were normal. Present drug and X-ray therapy is relatively ineffective in treating metastatic cancer of the adrenal medulla. Preliminary results in five patients indicate that, for the first time, a complex organic molecule can carry 131I into adrenal neoplasms reproducibly and in therapeutically effective doses of irradiation. We may also be able to select which patients will respond to therapeutic doses of 131I-MIBG and which patients will not respond.

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