How to standardize the diagnostic approach to pituitary neuroendocrine tumors.

IF 2.5 Q3 ENDOCRINOLOGY & METABOLISM
Sofia Asioli, Federica Guaraldi, M. Zoli, D. Mazzatenta, Chiara Villa
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Abstract

Pituitary tumors present heterogeneous biochemical, clinico-radiological, and histological features. Although histologically benign, a non-negligible number of cases present an unpredictable aggressive behavior with local invasiveness, partial/complete resistance to treatment and/or recurrence after surgery, and, rarely, metastasize, overall leading to a significant increase of morbidity, and, thus, requiring skilled multidisciplinary management in referral Centers. Histopathological diagnosis is essential to stratify cancer patient risk and uniform follow-up among Centers. Classification of pituitary neoplasia is continuously evolving in relation to the increased knowledge of mechanisms underlying adenohypophyseal cell tumorigenesis, and the attempts of combining clinico-radiological, biochemical, intraoperative, histological, and molecular elements, with the aim of identifying aggressive forms through. An integrated standardized histopathological report has been proposed in 2019 by the European Pituitary Pathology Group, based on the indications of the 2017 WHO classification of pituitary tumors. The last edition of the WHO Classification of Central Nervous System Tumors and of Endocrine and Neuroendocrine Tumors brought substantial novelties: 1) the replacement of the term "adenoma" with "Pituitary Neuroendocrine Tumor" (PitNET), and of "carcinoma" with "metastatic PitNET," and the consequent ICD-11 recoding from benign to malignant disease; and 2) the pivotal role of lineage restricted pituitary transcription factors for histological typing and subtyping. However, this approach does not reflect the spectrum of tumor phenotypes based on hormone secretion, nor include molecular features. Efforts of interdisciplinary groups of pituitary experts should be strongly encouraged to better understand factors involved in PitNETs evolution and, consequently, standardize diagnosis and reporting based on the most recent knowledges, essential to stratify cancer patient risk and uniform follow-up among centers.
如何规范垂体神经内分泌肿瘤的诊断方法。
垂体瘤具有不同的生化、临床放射学和组织学特征。虽然组织学上是良性的,但也有不可忽视的一部分病例表现出不可预测的侵袭性,具有局部侵袭性、部分/完全耐药和/或术后复发,极少数会发生转移,总体上导致发病率显著增加,因此需要转诊中心进行熟练的多学科管理。组织病理学诊断对癌症患者的风险分层和各中心的统一随访至关重要。随着人们对腺垂体细胞肿瘤发生机制认识的加深,以及将临床放射学、生化、术中、组织学和分子元素相结合的尝试,垂体肿瘤的分类也在不断发展,目的是通过这些元素来识别侵袭性肿瘤。欧洲垂体病理学组根据2017年世卫组织垂体瘤分类的指示,于2019年提出了综合标准化组织病理学报告。上一版《世界卫生组织中枢神经系统肿瘤及内分泌和神经内分泌肿瘤分类》带来了实质性的新变化:1)用 "垂体神经内分泌肿瘤"(PitNET)取代了 "腺瘤",用 "转移性垂体神经内分泌肿瘤 "取代了 "癌",并随之将 ICD-11 从良性疾病重新编码为恶性疾病;以及 2)系限制性垂体转录因子在组织学分型和亚型中的关键作用。然而,这种方法并不能反映基于激素分泌的肿瘤表型谱,也不包括分子特征。应大力鼓励垂体专家跨学科小组的努力,以更好地了解 PitNETs 演变的相关因素,从而根据最新知识规范诊断和报告,这对癌症患者的风险分层和各中心的统一随访至关重要。
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来源期刊
CiteScore
4.60
自引率
0.00%
发文量
146
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