Root A W, Martinez C R
Department of Pediatrics, Department of Biochemistry and Molecular Biology, University of South Florida College of Medicine, Tampa, FL 33612, USA.
Trends Endocrinol Metab. 1992 Oct;3(8):283-7. doi: 10.1016/1043-2760(92)90138-q.
In patients with hypopituitarism, magnetic resonance (MR) imaging of the hypothalamus and pituitary has disclosed a high incidence of hypoplasia of the anterior pituitary lobe, attenuation or transection of the pituitary stalk, and formation of an "ectopic" posterior pituitary lobe at the base of the hypothalamus. These anatomic abnormalities may be associated with other congenital malformations of the central nervous system, or may be due to an in utero toxic or infectious insult, perinatal trauma, neonatal asphyxia and hypoxia, head injury, or hemorrhage into a pituitary adenoma. The progressive development of defects in pituitary hormone secretion in such patients is probably due to continued atrophy of an anterior pituitary remnant with a limited vascular supply unstimulated by hypothalamic neuropeptides. By contrast, in patients with isolated hypogonadotropic hypogonadism, hypothalamic pituitary anatomy is normal, although abnormalities of the olfactory sulcus are present in patients with anosmia and hypogonadotropism (Kallmann syndrome). In most patients with central diabetes insipidus, the neurohypophysis is absent on MR scan.
在垂体功能减退患者中,下丘脑和垂体的磁共振成像显示垂体前叶发育不全、垂体柄变细或中断以及下丘脑底部出现“异位”垂体后叶的发生率很高。这些解剖学异常可能与中枢神经系统的其他先天性畸形有关,也可能是由于子宫内的毒性或感染性损伤、围产期创伤、新生儿窒息和缺氧、头部受伤或垂体腺瘤出血所致。这类患者垂体激素分泌缺陷的逐渐发展可能是由于垂体前叶残余部分持续萎缩,其血管供应有限,未受到下丘脑神经肽的刺激。相比之下,在孤立性促性腺激素缺乏性性腺功能减退患者中,下丘脑垂体的解剖结构是正常的,尽管嗅觉减退和促性腺激素缺乏患者(卡尔曼综合征)存在嗅沟异常。在大多数中枢性尿崩症患者中,磁共振扫描显示神经垂体缺如。