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促纤维增生型和黏液乳头型星形细胞瘤的病理和遗传学研究进展。

Recent Progress in the Pathology and Genetics of Pilocytic and Pilomyxoid Astrocytomas.

机构信息

Division of Neuropathology, Department of Pathology, UCSF School of Medicine, California, USA

Department of Pathology, Tan Tock Seng Hospital, Novena, Singapore

出版信息

Balkan Med J. 2019 Jan 1;36(1):3-11. doi: 10.4274/balkanmedj.2018.1001. Epub 2018 Jul 9.

Abstract

Pilocytic and pilomyxoid astrocytomas are some of the most common gliomas in children and young adults. These gliomas are indolent neoplasms with long overall survival probability. The genetic characteristics of these neoplasms are well known, and our deepened understanding of their associated molecular alterations has led to the development of novel treatment strategies and approaches. Currently, we can account for some of the unusual behavior, such as oncogene-induced senescence, associated spontaneous regression, anaplastic transformation, and cerebrospinal dissemination, of these gliomas. Nevertheless, enigmatic issues continue to surround these chronic tumors. Here, we review the classical and uncommon clinical pathological and genetic features of these indolent gliomas.

摘要

毛细胞型星形细胞瘤和毛细胞黏液型星形细胞瘤是儿童和青少年中最常见的胶质瘤之一。这些胶质瘤是惰性肿瘤,总体生存概率较长。这些肿瘤的遗传特征已被充分了解,我们对其相关分子改变的深入理解导致了新的治疗策略和方法的发展。目前,我们可以解释这些胶质瘤的一些异常行为,如癌基因诱导的衰老、自发性消退、间变转化和脑脊液播散等。然而,这些慢性肿瘤仍存在一些悬而未决的问题。在这里,我们回顾了这些惰性胶质瘤的经典和罕见的临床病理及遗传学特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc83/6335931/a6ddccb3ec9a/BMJ-36-3-g1.jpg

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