Losa M, Magnani P, Mortini P, Persani L, Acerno S, Giugni E, Songini C, Fazio F, Beck-Peccoz P, Giovanelli M
Department of Neurosurgery, IRCCS San Raffaele, University of Milan, Italy.
Eur J Nucl Med. 1997 Jul;24(7):728-31. doi: 10.1007/BF00879659.
Few data are available on the visualization of somatostatin receptors in vivo in patients with thyrotropin (TSH)-secreting adenoma. We studied five patients with TSH-secreting adenomas using single-photon emission tomography (SPET) after administration of indium-111 pentetreotide. The intensity of 111In-pentetreotide uptake by the tumours was correlated with the degree of TSH suppression after a single administration of 100 microg octreotide s. c. Five patients (three women and two men) aged 27-46 years were investigated. Except for one patient with acromegaly, all had pure TSH-secreting tumours. One patient was previously untreated, while two had received octreotide, one antithyroid drugs, and one radioiodine. In all patients SPET demonstrated increased uptake of 111In-pentetreotide by the pituitary adenoma. The target to non-target ratio (T/nT) of 111In-pentetreotide uptake was higher than 10 in three patients. Administration of 100 microg octreotide s. c. caused a significant reduction in TSH levels from 4.8+/-1.4 mU/l to a nadir of 3.1+/-1.1 mU/l after 6 h (P<<0.001 by ANOVA). Suppression of TSH secretion ranged from 30% to 60% of the baseline value. The T/nT ratio showed a trend toward a direct relationship with the degree of TSH inhibition after acute octreotide administration (r=0.67; P=NS). Our study showed that 111In-pentetreotide scan visualized somatostatin receptors in all five of the patients with TSH-secreting pituitary adenomas, confirming the frequent presence of somatostatin receptors in these rare tumours, even though the correlation with the TSH inhibition after a single administration of octreotide did not reach significance.
关于促甲状腺激素(TSH)分泌性腺瘤患者体内生长抑素受体可视化的可用数据很少。我们对5例TSH分泌性腺瘤患者在给予铟-111喷替肽后使用单光子发射断层扫描(SPET)进行了研究。肿瘤对111In-喷替肽的摄取强度与单次皮下注射100μg奥曲肽后TSH的抑制程度相关。对5例年龄在27至46岁之间的患者(3名女性和2名男性)进行了调查。除1例肢端肥大症患者外,所有患者均为单纯TSH分泌性肿瘤。1例患者此前未接受过治疗,2例接受过奥曲肽治疗,1例接受过抗甲状腺药物治疗,1例接受过放射性碘治疗。在所有患者中,SPET均显示垂体腺瘤对111In-喷替肽的摄取增加。3例患者的111In-喷替肽摄取的靶与非靶比值(T/nT)高于10。皮下注射100μg奥曲肽使TSH水平从4.8±1.4mU/L显著降低至6小时后的最低点3.1±1.1mU/L(方差分析,P<<0.001)。TSH分泌的抑制范围为基线值的30%至60%。急性给予奥曲肽后,T/nT比值显示出与TSH抑制程度呈直接关系的趋势(r = 0.67;P = 无显著性差异)。我们的研究表明,111In-喷替肽扫描在所有5例TSH分泌性垂体腺瘤患者中均使生长抑素受体可视化,证实了这些罕见肿瘤中生长抑素受体的频繁存在,尽管单次给予奥曲肽后与TSH抑制的相关性未达到显著性。