Arasho B D, Schaller B, Sandu N, Zenebe G
Department of Neurology, Faculty of Medicine, Addis Ababa University, Ethiopia.
Exp Clin Endocrinol Diabetes. 2009 Nov;117(10):567-72. doi: 10.1055/s-0029-1202831. Epub 2009 Apr 16.
Pituitary adenomas account for about 10% of all intracranial neoplasms and for about 85% of all pituitary tumors. In addition, prospective studies of normal persons and postmortem examinations reveal pituitary adenomas in up to 10% of adults indicating that not all pituitary adenomas are clinically significant. With clinically significant pituitary adenomas, patients may present with hyper- or under-secretion of pituitary hormones or with symptoms and signs of space occupying intracranial tumor like headache and visual compromise. Like other differentiated neuroendocrine cells, the anterior pituitary displays remarkable plasticity in response to physiological demands, as exemplified by the lactotroph differentiation and proliferation of pregnancy or the thyrotroph hyperplasia of primary hypothyroidism. These reversible changes are mediated by a diverse array of signals that have been interpreted to support a role for hormonal stimulation in the pathogenesis of pituitary adenomas. Different investigators have shown a tendency to gender-related differences not only in surgical outcome, but also in the presenting symptoms and signs, duration of symptoms, tumor size, tumor histology, and restoration of normal pituitary function in patients who are surgically treated and histologically proven pituitary adenomas. In this review, we will try to give a systematic insight into gender related differences of pituitary adenomas. Special reference is given on potential different biology of these tumors as suggested by the gender related differences. The manuscript therefore gives new insights into the cellular understanding of the pituitary adenomas.
垂体腺瘤约占所有颅内肿瘤的10%,占所有垂体肿瘤的约85%。此外,对正常人的前瞻性研究和尸检显示,高达10%的成年人存在垂体腺瘤,这表明并非所有垂体腺瘤都具有临床意义。对于具有临床意义的垂体腺瘤,患者可能表现为垂体激素分泌过多或过少,或出现颅内占位性肿瘤的症状和体征,如头痛和视力受损。与其他分化的神经内分泌细胞一样,垂体前叶在应对生理需求时表现出显著的可塑性,例如妊娠时催乳素细胞的分化和增殖或原发性甲状腺功能减退时促甲状腺细胞增生。这些可逆变化由多种信号介导,这些信号被解释为支持激素刺激在垂体腺瘤发病机制中的作用。不同的研究者发现,对于接受手术治疗且经组织学证实为垂体腺瘤的患者,不仅在手术结果方面,而且在症状和体征、症状持续时间、肿瘤大小、肿瘤组织学以及垂体功能恢复方面,都存在与性别相关的差异倾向。在本综述中,我们将试图系统地深入了解垂体腺瘤的性别相关差异。特别参考了这些肿瘤可能因性别相关差异而具有不同生物学特性的情况。因此,本文稿为垂体腺瘤的细胞理解提供了新的见解。