Poorly differentiated chordoma showing loss of SMARCB1/INI1: Clinicopathological and radiological spectrum of nine cases, including uncommon features of a relatively under-recognized entity

Rekhi, Bharat; Michal, Michael; ERGEN, FATMA; Roy, Paromita; Puls, Florian; Haugland, Hans; Soylemezoglu, Figen; KÖSEMEHMETOĞLU, KEMAL

doi:10.1016/j.anndiagpath.2021.151809

Poorly differentiated chordoma showing loss of SMARCB1/INI1: Clinicopathological and radiological spectrum of nine cases, including uncommon features of a relatively under-recognized entity

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Rekhi B., Michal M., ERGEN F. B., Roy P., Puls F., Haugland H. K., ...More

ANNALS OF DIAGNOSTIC PATHOLOGY, vol.55, 2021 (SCI-Expanded)

Publication Type: Article / Article
Volume: 55
Publication Date: 2021
Doi Number: 10.1016/j.anndiagpath.2021.151809
Journal Name: ANNALS OF DIAGNOSTIC PATHOLOGY
Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, EMBASE, MEDLINE
Keywords: Poorly differentiated chordoma, INI1, SAMRCB1, Brachyury, Notochordal tumors, Rare bone tumors, BRACHYURY EXPRESSION, TUMORS, IMMUNOEXPRESSION, INVOLVEMENT, INI1, RARE
Hacettepe University Affiliated: Yes

Abstract

Poorly differentiated chordoma is a newly recognized entity in the recent World Health Organization (WHO) classification of tumors of soft tissue and bone. Slightly over 60 such cases have been documented.