Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Surg Pathol Clin. 2023 Mar;16(1):119-129. doi: 10.1016/j.path.2022.09.011.
There is increasing recognition of the high prevalence of hereditary predisposition syndromes in patients diagnosed with paraganglioma/pheochromocytoma. It is widely acknowledged that germline pathogenic alterations of the succinate dehydrogenase complex genes (SDHA, SDHB, SDHC, SDHD, SDHAF2) contribute to the pathogenesis of most of these tumors. Herein, we have provided an update on the biology and diagnosis of succinate dehydrogenase-deficient paraganglioma/pheochromocytoma, including the molecular biology of the succinate dehydrogenase complex, mechanisms and consequences of inactivation of this complex, the prevalence of pathogenic alterations, and patterns of inheritance.
越来越多的人认识到,患有副神经节瘤/嗜铬细胞瘤的患者中存在高发的遗传性倾向综合征。人们普遍认为,琥珀酸脱氢酶复合物基因(SDHA、SDHB、SDHC、SDHD、SDHAF2)的种系致病性改变导致了这些肿瘤中的大多数发生。本文就琥珀酸脱氢酶缺陷型副神经节瘤/嗜铬细胞瘤的生物学和诊断进行了更新,包括琥珀酸脱氢酶复合物的分子生物学、该复合物失活的机制和后果、致病性改变的发生率以及遗传模式。