Cancer Diagnosis and Pathology Group, Kolling Institute of Medical Research, Royal North Shore Hospital, St Leonards, NSW, Australia.
University of Sydney, Sydney, NSW, Australia.
Histopathology. 2018 Jan;72(1):97-105. doi: 10.1111/his.13402.
Phaeochromocytoma and paraganglioma (PHEO/PGL) are rare tumours with an estimated annual incidence of 3 per million. Advances in molecular understanding have led to the recognition that at least 30-40% arise in the setting of hereditary disease. Germline mutations in the succinate dehydrogenase genes SDHA, SDHB, SDHC, SDHD and SDHAF2 are the most prevalent of the more than 19 hereditary genetic abnormalities which have been reported. It is therefore recommended that, depending on local resources and availability, at least some degree of genetic testing should be offered to all PHEO/PGL patients, including those with clinically sporadic disease. It is now accepted that that all PHEO/PGL have some metastatic potential; therefore, concepts of benign and malignant PHEO/PGL have no meaning and have been replaced by a risk stratification approach. Although there is broad acceptance that certain features, including high proliferative activity, invasive growth, increased cellularity, large tumour nests and comedonecrosis, are associated with an increased risk of metastasis, it remains difficult to predict the clinical behaviour of individual tumours and no single risk stratification scheme is endorsed or in widespread use. In this review, we provide an update on advances in the pathology and genetics of PHEO/PGL with an emphasis on the changes introduced in the WHO 2017 classification of endocrine neoplasia relevant to practising surgical pathologists.
嗜铬细胞瘤和副神经节瘤(PHEO/PGL)是罕见的肿瘤,估计每年的发病率为每百万分之三。分子理解的进步导致人们认识到,至少有 30-40%的肿瘤发生在遗传性疾病的背景下。琥珀酸脱氢酶基因 SDHA、SDHB、SDHC、SDHD 和 SDHAF2 的种系突变是报道的 19 种以上遗传性遗传异常中最常见的。因此,建议根据当地资源和可用性,向所有 PHEO/PGL 患者提供某种程度的基因检测,包括临床散发性疾病患者。现在人们普遍认为所有 PHEO/PGL 都有一定的转移潜力;因此,良性和恶性 PHEO/PGL 的概念没有意义,已被风险分层方法所取代。尽管人们普遍认为某些特征,包括高增殖活性、侵袭性生长、细胞增多、大肿瘤巢和坏死性囊变,与转移风险增加有关,但仍然难以预测个别肿瘤的临床行为,并且没有单一的风险分层方案得到认可或广泛使用。在这篇综述中,我们提供了 PHEO/PGL 病理学和遗传学进展的最新信息,重点介绍了与实践外科病理学家相关的 WHO 2017 年内分泌肿瘤分类中引入的变化。