Bethge N, Ahuja S, Diel F, Usadel K H
Institut für Pathologie, Universitätsklinikum Steglitz, Freie Universität Berlin, BRD.
Exp Clin Endocrinol. 1988 May;91(2):217-22. doi: 10.1055/s-0029-1210748.
The presence of somatostatin-immunoreactivity in tumor tissue of adrenal pheochromocytoma and thyroid medullary carcinoma identified by peroxidase-antiperoxidase technique is reported in one case of Sipple syndrome. This patient was found to have a high concentration of somatostatin-immunoreactivity in the peripheral blood (40 ng/l, normal 0-20 ng/l). After removal of the tumors, the plasma somatostatin-immunoreactivity fell within normal range (12.5 ng/l). This seems to be the first report of Sipple syndrome that produces somatostatin-immunoreactivity in both: pheochromocytoma and thyroid medullary carcinoma.
本文报道了1例多发性内分泌腺瘤病(Sipple综合征)患者,应用过氧化物酶-抗过氧化物酶技术,在肾上腺嗜铬细胞瘤和甲状腺髓样癌的肿瘤组织中发现了生长抑素免疫反应性。该患者外周血中生长抑素免疫反应性浓度较高(40 ng/l,正常范围0-20 ng/l)。肿瘤切除后,血浆生长抑素免疫反应性降至正常范围(12.5 ng/l)。这似乎是首例在嗜铬细胞瘤和甲状腺髓样癌中均产生生长抑素免疫反应性的Sipple综合征报告。