Oldfield Edward H, Merrill Marsha J
1Department of Neurological Surgery, University of Virginia Health Sciences Center, University of Virginia, Charlottesville, Virginia; and.
2Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland.
J Neurosurg. 2015 Jun;122(6):1444-9. doi: 10.3171/2014.10.JNS141720. Epub 2015 Apr 10.
Pituitary adenomas occasionally undergo infarction, apoplexy, which often destroys much of the tumor. It is well known that apoplexy can be precipitated by several acute factors, including cardiac surgery, other types of surgery, trauma, insulin infusion, and stimulation with administration of hypothalamic releasing factors.
The prior focus on mechanisms underlying pituitary apoplexy has been on these acute events. Less attention has been given to the endogenous features of pituitary tumors that make them susceptible to spontaneous infarction, despite that most pituitary apoplexy occurs in the absence of a recognized precipitating event. The authors examine intrinsic features of pituitary adenomas that render them vulnerable to apoplexy-features such as high metabolic demand, paucity of angiogenesis, and sparse vascularity, qualities that have previously not been linked with apoplexy-and argue that it is these features of adenomas that underlie their susceptibility to spontaneous infarction. The sensitivity of freshly cultured pituitary adenomas to hypoglycemia is assessed.
Adenomas have high metabolic demand, limited angiogenesis, and reduced vessel density compared with the normal gland. Pituitary adenoma cells do not survive in the presence of reduced or absent concentrations of glucose.
The authors propose that the frequent ischemic infarction of pituitary adenomas is the product of intrinsic features of these tumors. These endogenous qualities create a tenuous balance between high metabolic demand and marginal tissue perfusion. Thus, the tumor is vulnerable to spontaneous infarction or to acute ischemia by any event that acutely alters the balance between tumor perfusion and tumor metabolism, events such as acute systemic hypotension, abruptly decreased supply of nutrients, hypoglycemia with insulin administration, or increase in the tumor's metabolic demand due to administration of hypothalamic releasing factors. It may be possible to take advantage of these intrinsic features of pituitary adenomas by using aspects of this vulnerability for development of new approaches for treatment.
垂体腺瘤偶尔会发生梗死,即卒中,这通常会破坏大部分肿瘤组织。众所周知,卒中可由多种急性因素诱发,包括心脏手术、其他类型的手术、创伤、胰岛素输注以及下丘脑释放因子的刺激。
以往对垂体卒中潜在机制的关注主要集中在这些急性事件上。尽管大多数垂体卒中发生在没有公认诱发事件的情况下,但垂体肿瘤使其易发生自发性梗死的内在特征却较少受到关注。作者研究了垂体腺瘤使其易发生卒中的内在特征,如高代谢需求、血管生成不足和血管稀疏等,这些特征以前并未与卒中相关联,并认为正是腺瘤的这些特征导致了它们易发生自发性梗死。评估了新鲜培养的垂体腺瘤对低血糖的敏感性。
与正常腺体相比,腺瘤具有高代谢需求、有限的血管生成和降低的血管密度。垂体腺瘤细胞在葡萄糖浓度降低或缺乏的情况下无法存活。
作者提出垂体腺瘤频繁发生缺血性梗死是这些肿瘤内在特征的产物。这些内在特性在高代谢需求和边缘组织灌注之间形成了脆弱的平衡。因此,肿瘤容易发生自发性梗死或因任何急性改变肿瘤灌注与肿瘤代谢之间平衡的事件而发生急性缺血,这些事件如急性全身性低血压、营养物质供应突然减少、胰岛素给药导致的低血糖或下丘脑释放因子给药导致肿瘤代谢需求增加。利用垂体腺瘤的这些内在特征,有可能通过利用这种易损性来开发新的治疗方法。