TY - JOUR
T1 - EWSR1::POU2AF3(COLCA2) Sarcoma: An Aggressive, Polyphenotypic Sarcoma With a Head and Neck Predilection
AU - Koshyk, Olena
AU - Dehner, Carina A.
AU - van den Hout, Mari F.C.M.
AU - Bempt, Isabelle Vanden
AU - Sciot, Raf
AU - Huang, Hsuan Ying
AU - Agaimy, Abbas
AU - Din, Nasir Ud
AU - Klubíčková, Natálie
AU - Mosaieby, Elaheh
AU - Skálová, Alena
AU - Michalová, Květoslava
AU - Schöffski, Patrick
AU - Oliveira, Andre M.
AU - Halling, Kevin C.
AU - Gupta, Sounak
AU - Gross, John M.
AU - Nin, Johanna W.M.
AU - Michal, Michal
AU - Folpe, Andrew L.
AU - Kosemehmetoglu, Kemal
AU - Torres-Mora, Jorge
AU - Michal, Michael
N1 - Publisher Copyright:
© 2023 United States & Canadian Academy of Pathology
PY - 2023/12
Y1 - 2023/12
N2 - EWSR1::POU2AF3 (COLCA2) sarcomas are a recently identified group of undifferentiated round/spindle cell neoplasms with a predilection for the head and neck region. Herein, we report our experience with 8 cases, occurring in 5 men and 3 women (age range, 37-74 years; median, 60 years). Tumors involved the head/neck (4 cases), and one each the thigh, thoracic wall, fibula, and lung. Seven patients received multimodal therapy; 1 patient was treated only with surgery. Clinical follow-up (8 patients; range, 4-122 months; median, 32 months) showed 5 patients with metastases (often multifocal, with a latency ranging from 7 to 119 months), and 3 of them also with local recurrence. The median local recurrence–free and metastasis-free survival rates were 24 months and 29 months, respectively. Of the 8 patients, 1 died of an unknown cause, 4 were alive with metastatic disease, 1 was alive with unresectable local disease, and 2 were without disease. The tumors were composed of 2 morphologic subgroups: (1) relatively bland tumors consisting of spindled to stellate cells with varying cellularity and fibromyxoid stroma (2 cases) and (2) overtly malignant tumors composed of nests of “neuroendocrine-appearing” round cells surrounded by spindled cells (6 cases). Individual cases in the second group showed glandular, osteogenic, or rhabdomyoblastic differentiation. Immunohistochemical results included CD56 (4/4 cases), GFAP (5/8), SATB2 (4/6), keratin (AE1/AE3) (5/8), and S100 protein (4/7). RNA sequencing identified EWSR1::POU2AF3 gene fusion in all cases. EWSR1 gene rearrangement was confirmed by fluorescence in situ hybridization in 5 cases. Our findings confirm the head/neck predilection and aggressive clinical behavior of EWSR1::POU2AF3 sarcomas and widen the morphologic spectrum of these rare lesions to include relatively bland spindle cell tumors and tumors with divergent differentiation.
AB - EWSR1::POU2AF3 (COLCA2) sarcomas are a recently identified group of undifferentiated round/spindle cell neoplasms with a predilection for the head and neck region. Herein, we report our experience with 8 cases, occurring in 5 men and 3 women (age range, 37-74 years; median, 60 years). Tumors involved the head/neck (4 cases), and one each the thigh, thoracic wall, fibula, and lung. Seven patients received multimodal therapy; 1 patient was treated only with surgery. Clinical follow-up (8 patients; range, 4-122 months; median, 32 months) showed 5 patients with metastases (often multifocal, with a latency ranging from 7 to 119 months), and 3 of them also with local recurrence. The median local recurrence–free and metastasis-free survival rates were 24 months and 29 months, respectively. Of the 8 patients, 1 died of an unknown cause, 4 were alive with metastatic disease, 1 was alive with unresectable local disease, and 2 were without disease. The tumors were composed of 2 morphologic subgroups: (1) relatively bland tumors consisting of spindled to stellate cells with varying cellularity and fibromyxoid stroma (2 cases) and (2) overtly malignant tumors composed of nests of “neuroendocrine-appearing” round cells surrounded by spindled cells (6 cases). Individual cases in the second group showed glandular, osteogenic, or rhabdomyoblastic differentiation. Immunohistochemical results included CD56 (4/4 cases), GFAP (5/8), SATB2 (4/6), keratin (AE1/AE3) (5/8), and S100 protein (4/7). RNA sequencing identified EWSR1::POU2AF3 gene fusion in all cases. EWSR1 gene rearrangement was confirmed by fluorescence in situ hybridization in 5 cases. Our findings confirm the head/neck predilection and aggressive clinical behavior of EWSR1::POU2AF3 sarcomas and widen the morphologic spectrum of these rare lesions to include relatively bland spindle cell tumors and tumors with divergent differentiation.
KW - COLCA2
KW - EWSR1::POU2AF3
KW - gene fusion
KW - neuroendocrine-like
KW - sarcoma
KW - sinonasal tract
KW - soft tissues
KW - spindle cell sarcoma
UR - http://www.scopus.com/inward/record.url?scp=85181178172&partnerID=8YFLogxK
U2 - 10.1016/j.modpat.2023.100337
DO - 10.1016/j.modpat.2023.100337
M3 - Article
C2 - 37742928
AN - SCOPUS:85181178172
SN - 0893-3952
VL - 36
JO - Modern Pathology
JF - Modern Pathology
IS - 12
M1 - 100337
ER -