Bevan J S, Asa S L, Rossi M L, Esiri M M, Adams C B, Burke C W
Department of Endocrinology, Radcliffe Infirmary, Oxford, UK.
Clin Endocrinol (Oxf). 1989 Mar;30(3):213-24. doi: 10.1111/j.1365-2265.1989.tb02229.x.
A 74-year-old acromegalic found to have an intrasellar gangliocytocytoma and GH-secreting pituitary adenoma is described. The gangliocytoma contained immunoreactive gastrin and, to a lesser extent, GHRH, and the adenoma immunostained for GH. Gastrin has not been previously reported in hypothalamic gangliocytomas. Since this peptide has been demonstrated in normal hypothalamus and pituitary, and provokes GH release when administered intraventricularly, it may have caused GHRH release from the gangliocytoma by a local paracrine action and led to adenoma formation and acromegaly.
本文描述了一名74岁的肢端肥大症患者,发现其患有鞍内神经节细胞瘤和分泌生长激素的垂体腺瘤。神经节细胞瘤含有免疫反应性胃泌素,程度较轻的还有生长激素释放激素(GHRH),而腺瘤对生长激素呈免疫染色阳性。此前下丘脑神经节细胞瘤中尚未有胃泌素的报道。由于这种肽已在正常下丘脑和垂体中得到证实,并且脑室内给药时可刺激生长激素释放,它可能通过局部旁分泌作用导致神经节细胞瘤释放生长激素释放激素,并进而导致腺瘤形成和肢端肥大症。