CNS Low-grade Diffusely Infiltrative Tumors With INI1 Deficiency, Possessing a High Propensity to Progress to Secondary INI1-deficient Rhabdoid Tumors-Reference-Cited by-同舟云学术

CNS Low-grade Diffusely Infiltrative Tumors With INI1 Deficiency, Possessing a High Propensity to Progress to Secondary INI1-deficient Rhabdoid Tumors

Published:2020-06-23 Issue:11 Volume:44 Page:1459-1468
ISSN:0147-5185
Container-title:American Journal of Surgical Pathology
language:en
Short-container-title:

Author:

Nobusawa Sumihito,Nakata Satoshi,Nakano Yoshiko,Kawamura Atsufumi,Yoshida Makiko,Tamura Akihiro,Hasegawa Daiichiro,Kosaka Yoshiyuki,Ito Ichiro,Watanabe Reiko,Oishi Takuma,Hayashi Nakamasa,Ishikawa Eiichi,Sakamoto Noriaki,Okura Naoki,Murakami Chiaki,Ichimura Koichi,Hirato Junko,Yokoo Hideaki

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

Reference35 articles.

1. Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood;Rorke;J Neurosurg,1996

2. Atypical teratoid/rhabdoid tumors are comprised of three epigenetic subgroups with distinct enhancer landscapes;Johann;Cancer Cell,2016

3. Atypical teratoid/rhabdoid tumor (AT/RT) arising from ependymoma: a type of AT/RT secondarily developing from other primary central nervous system tumors;Nobusawa;J Neuropathol Exp Neurol,2016

4. Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study;Allen;Neuro Oncol,2006

5. Atypical teratoid/rhabdoid tumor arising in a ganglioglioma: genetic characterization;Kleinschmidt-DeMasters;Am J Surg Pathol,2011

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A 7‐year‐old boy presented with temporal lobe lesion;Brain Pathology;2024-02-14

2. An infantile pineal embryonal tumor showing pathological features of a CNS ganglioneuroblastoma and the methylation profiling of an atypical teratoid/rhabdoid tumor and SMARCA4 mutation;Journal of Neuropathology & Experimental Neurology;2023-06-20

3. A clinicopathological analysis of supratentorial ependymoma, ZFTA fusion-positive: utility of immunohistochemical detection of CDKN2A alterations and characteristics of the immune microenvironment;Brain Tumor Pathology;2023-06-16

4. A clinicopathological analysis of supratentorial ependymoma, ZFTA fusion-positive: Utility of immunohistochemical detection of CDKN2A alterations and characteristics of the immune microenvironment.;2023-03-10

5. SMARCB1-deficient and SMARCA4-deficient Malignant Brain Tumors With Complex Copy Number Alterations and TP53 Mutations May Represent the First Clinical Manifestation of Li-Fraumeni Syndrome;American Journal of Surgical Pathology;2022-04-22