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

Atıf İçin Kopyala

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

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

Yayın Türü: Makale / Tam Makale
Cilt numarası: 55
Basım Tarihi: 2021
Doi Numarası: 10.1016/j.anndiagpath.2021.151809
Dergi Adı: ANNALS OF DIAGNOSTIC PATHOLOGY
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, EMBASE, MEDLINE
Anahtar Kelimeler: Poorly differentiated chordoma, INI1, SAMRCB1, Brachyury, Notochordal tumors, Rare bone tumors, BRACHYURY EXPRESSION, TUMORS, IMMUNOEXPRESSION, INVOLVEMENT, INI1, RARE
Hacettepe Üniversitesi Adresli: Evet

Özet

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.