Mahta Ali, Haghpanah Vahid, Lashkari Anahita, Heshmat Ramin, Larijani Bagher, Tavangar Seyed Mohammad
Dr. Shariati Hospital, North Kargar Avenue, Tehran, Iran.
Folia Neuropathol. 2007;45(2):72-7.
Pituitary adenomas without clinically active hypersecretion are summarized under the term non-functioning pituitary adenoma (NFPA). Since there are no specific serum markers, the differential diagnosis and treatment imply special difficulties. By using immunohistochemical methods we will have new insight into the nature and pathogenesis of these tumours. Ki-67 is a nuclear antigen detected by the monoclonal antibody MIB-1 and its labelling index (LI) is considered a marker of normal and abnormal cell proliferation. The aim of this study was to investigate the possible role of immunohistochemistry and MIB1-LI determination in NFPAs to predict tumoural behaviour and better management. In this clinicopathological study, 85 cases of NFPAs were analysed immunohistochemically. MIB1-LI was also determined in studied cases. Clinical presentation, treatment and follow-up data were also reviewed and the correlation between clinical and pathologic findings was established. Eighteen adenomas (21.2%) were immunoreactive to one or two adenohypophysial hormones of which 4 GH positive adenomas had aggressive behaviour (2 significant juxtasellar extensions and 2 recurrences). MIB-1 LI was more than 5% in only 5 cases including 2 invasive adenomas but with no evidence of recurrence. No significant statistical difference between clinical presentations in immunoreactive and non-immunoreactive NFPAs was observed except for unilateral temporal hemianopia which was more common in immunoreactive adenomas (P=0.022). NFPAs comprise several pathologically different types of tumours, some of which are potentially hormone producing, but some defects in hormone secretion or production of biologically inactive or insufficient amount of hormone may be the culprit in the lack of evidence of rising serum hormone levels. MIB-1 LI may be indicative of invasiveness but not a predictor of recurrence. Silent somatotropinomas may have more aggressive behaviour in comparison with other NFPAs.
无临床活性分泌亢进的垂体腺瘤被归纳在无功能垂体腺瘤(NFPA)这一术语之下。由于没有特异性血清标志物,其鉴别诊断和治疗存在特殊困难。通过免疫组化方法,我们将对这些肿瘤的性质和发病机制有新的认识。Ki-67是一种由单克隆抗体MIB-1检测的核抗原,其标记指数(LI)被认为是正常和异常细胞增殖的标志物。本研究的目的是探讨免疫组化和MIB1-LI测定在NFPA中预测肿瘤行为及更好管理方面的可能作用。在这项临床病理研究中,对85例NFPA进行了免疫组化分析。还在研究病例中测定了MIB1-LI。回顾了临床表现、治疗及随访数据,并建立了临床与病理结果之间的相关性。18例腺瘤(21.2%)对一种或两种腺垂体激素呈免疫反应性,其中4例生长激素阳性腺瘤具有侵袭性行为(2例有明显的鞍旁扩展,2例复发)。仅5例MIB-1 LI超过5%,包括2例侵袭性腺瘤,但无复发证据。除了单侧颞侧偏盲在免疫反应性腺瘤中更常见(P=0.022)外,免疫反应性和非免疫反应性NFPA的临床表现之间未观察到显著统计学差异。NFPA包括几种病理上不同类型的肿瘤,其中一些可能潜在地产生激素,但激素分泌缺陷或产生无生物活性或量不足的激素可能是血清激素水平升高缺乏证据的原因。MIB-1 LI可能提示侵袭性,但不是复发的预测指标。与其他NFPA相比,静默性生长激素瘤可能具有更具侵袭性的行为。