Srivastava Alok, Singh Manish, Yadav Awadhesh, Srivastava Chhitij, Chandra Anil, Srivastava Akanksha D
Department of Neurosurgery, Ganesh Shankar Vidyarthi Memorial Medical College, Kanpur, Uttar Pradesh, India.
Department of Neurosurgery, King George's Medical University, Lucknow, Uttar Pradesh, India.
Asian J Neurosurg. 2024 Jun 10;19(2):107-111. doi: 10.1055/s-0043-1777264. eCollection 2024 Jun.
The new World Health Organization nomenclature of pituitary tumors was introduced in the year 2022 after much deliberation. This nomenclature clearly demarcates the anterior lobe (adenohypophyseal), posterior lobe (neurohypophyseal), and hypothalamic tumors. There is also focus on other tumors arising in the sellar region. The nomenclature has also advocated the routine use of immunohistochemistry in describing the pituitary transcription factors that plays a fundamental role in distinguishing the cell lineage of these tumors. However, the nomenclature is complex in understanding due to inclusion of pathological correlates like transcription factors, hormones, biomarkers, and various controversies that have emerged regarding the renaming of pituitary adenomas (PA) as PiTNETs ("Pituitary Neuroendocrine tumors") because majority of the adenomas are benign and have rare metastatic behavior while classifying them as PiTNETs will create unnecessary misinterpretation of these as aggressive tumors that will lead to apprehension among the patients. The new classification gives deeper insight into the histological picture of the various pituitary tumors but other than contributing to the follow-up strategy and postsurgery management, this classification does not add anything new that could be advantageous for the neurosurgeons in clinical practice and decision making, especially in deciding the plan of action for surgery. Hence, there is need of a more comprehensive, integrated, neuroradiological-based classification with more emphasis on the invasiveness of these tumors that would assist the neurosurgeons in planning the treatment strategy and managing patients of pituitary tumors.
经过多方审议,世界卫生组织于2022年推出了垂体肿瘤的新命名法。该命名法明确划分了前叶(腺垂体)、后叶(神经垂体)和下丘脑肿瘤。同时也关注鞍区出现的其他肿瘤。该命名法还提倡在描述垂体转录因子时常规使用免疫组化,这些转录因子在区分这些肿瘤的细胞谱系方面起着至关重要的作用。然而,由于纳入了转录因子、激素、生物标志物等病理相关因素,以及垂体腺瘤(PA)重新命名为垂体神经内分泌肿瘤(PiTNETs)所引发的各种争议,该命名法理解起来较为复杂,因为大多数腺瘤是良性的,转移行为罕见,而将它们归类为PiTNETs会造成不必要的误解,让人们以为它们是侵袭性肿瘤,从而导致患者产生担忧。新的分类法能更深入地洞察各种垂体肿瘤的组织学情况,但除了有助于随访策略和术后管理外,该分类法并没有为神经外科医生在临床实践和决策中带来任何新的优势,尤其是在决定手术行动方案时。因此,需要一种更全面、综合、基于神经放射学的分类法,更加强调这些肿瘤的侵袭性,这将有助于神经外科医生规划治疗策略并管理垂体肿瘤患者。