Myxoid pleomorphic liposarcoma—a clinicopathologic, immunohistochemical, molecular genetic and epigenetic study of 12 cases, suggesting a possible relationship with conventional pleomorphic liposarcoma-Reference-Cited by-同舟云学术

Myxoid pleomorphic liposarcoma—a clinicopathologic, immunohistochemical, molecular genetic and epigenetic study of 12 cases, suggesting a possible relationship with conventional pleomorphic liposarcoma

Published:2021-06-24 Issue:11 Volume:34 Page:2043-2049
ISSN:0893-3952
Container-title:Modern Pathology
language:en
Short-container-title:Mod Pathol

Author:

Creytens David,Folpe Andrew L.,Koelsche Christian^ORCID,Mentzel Thomas,Ferdinande Liesbeth,van Gorp Joost M.,Van der Linden Malaïka,Raman Lennart^ORCID,Menten Björn,Fritchie Karen^ORCID,von Deimling Andreas^ORCID,Van Dorpe Jo^ORCID,Flucke Uta

Funder

Deutsche Krebshilfe

Publisher

Springer Science and Business Media LLC

Subject

Pathology and Forensic Medicine

Link

https://www.nature.com/articles/s41379-021-00862-2.pdf

Reference45 articles.

1. Alaggio R, Coffin CM, Weiss SW, Bridge JA, Issakov J, Oliveira AM, et al. Liposarcomas in young patients. A study of 82 cases occurring patients younger than 22 years of age. Am J Surg Pathol. 2009;33:645–58.

2. WHO Classification of Tumours Editorial Board. WHO Classification of Tumours of Soft Tissue and Bone. 5th ed. Lyon, France: IARC Press; 2020

3. Alaggio R, Creytens D. Myxoid pleomorphic liposarcoma. In: WHO Classification of Tumours of Soft tissue and Bone. 5th ed. Lyon, France: IARC; 2020