Low‐grade diffusely infiltrative tumour (LGDIT), SMARCB1‐mutant: A clinical and histopathological distinct entity showing epigenetic similarity with ATRT‐MYC-Reference-Cited by-同舟云学术

Low‐grade diffusely infiltrative tumour (LGDIT), SMARCB1‐mutant: A clinical and histopathological distinct entity showing epigenetic similarity with ATRT‐MYC

Published:2022-02-18 Issue:4 Volume:48 Page:
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathology Appl Neurobio

Author:

Hasselblatt Martin¹^ORCID,Thomas Christian¹,Federico Aniello²³,Bens Susanne⁴,Hellström Mats⁵,Casar‐Borota Olivera⁵⁶^ORCID,Kordes Uwe⁷,Neumann Julia E.⁸⁹^ORCID,Dottermusch Matthias⁸⁹,Rodriguez Fausto J.¹⁰^ORCID,Lo Andrea C.¹¹,Cheng Sylvia¹²,Hendson Glenda¹³,Hukin Juliette¹²,Hartmann Christian¹⁴,Koch Arend¹⁵,Capper David¹⁵¹⁶,Siebert Reiner⁴,Paulus Werner¹,Nemes Karolina¹⁷,Johann Pascal D.²³¹⁷,Frühwald Michael C.¹⁷,Kool Marcel²³¹⁸

Affiliation:

1. Institute of Neuropathology University Hospital Münster Münster Germany

2. Hopp Children's Cancer Center (KiTZ) Heidelberg Germany

3. Division of Paediatric Neurooncology German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK) Heidelberg Germany

4. Institute of Human Genetics Ulm University and Ulm University Medical Center Ulm Germany

5. Department of Immunology, Genetics and Pathology, Rudbeck Laboratory Uppsala University Uppsala Sweden

6. Department of Clinical Pathology Uppsala University Hospital Uppsala Sweden

7. Department of Pediatric Hematology and Oncology University Medical Center Hamburg Germany

8. Institute of Neuropathology University Medical Center Hamburg Germany

9. Center for Molecular Neurobiology Hamburg (ZMNH) University Medical Center Hamburg‐Eppendorf Hamburg Germany

10. Department of Pathology The Johns Hopkins University School of Medicine Baltimore Maryland USA

11. Radiation Oncology British Columbia Cancer and University of British Columbia Vancouver Canada

12. Division of Hematology, Oncology and BMT, Department of Pediatrics University of British Columbia Vancouver Canada

13. Department of Pathology BC Women and Children's Hospital Vancouver Canada

14. Department of Neuropathology, Institute of Pathology Hannover Medical School Hannover Germany

15. Department of Neuropathology Charité ‐ Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt‐Universität zu Berlin Berlin Germany

16. German Cancer Consortium (DKTK), Partner Site Berlin German Cancer Research Center (DKFZ) Heidelberg Germany

17. Pediatric and Adolescent Medicine, Swabian Childrens' Cancer Center University Childrens' Hospital Medical Center Augsburg and EU‐RHAB Registry Augsburg Germany

18. Princess Máxima Center for Pediatric Oncology Utrecht Netherlands

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nan.12797

Reference13 articles.

1. Atypical teratoid/rhabdoid tumors—current concepts, advances in biology, and potential future therapies

2. Molecular subgrouping of atypical teratoid/rhabdoid tumors—a reinvestigation and current consensus

3. Sellar Region Atypical Teratoid/Rhabdoid Tumors (ATRT) in Adults Display DNA Methylation Profiles of the ATRT-MYC Subgroup

4. Atypical Teratoid/Rhabdoid Tumor (AT/RT) With Molecular Features of Pleomorphic Xanthoastrocytoma

5. Atypical Teratoid/Rhabdoid Tumor Arising in a Ganglioglioma

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