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EWSR1::POU2AF3(COLCA2) Sarcoma: An Aggressive, Polyphenotypic Sarcoma With a Head and Neck Predilection

  • Olena Koshyk
  • , Carina A. Dehner
  • , Mari F.C.M. van den Hout
  • , Isabelle Vanden Bempt
  • , Raf Sciot
  • , Hsuan Ying Huang
  • , Abbas Agaimy
  • , Nasir Ud Din
  • , Natálie Klubíčková
  • , Elaheh Mosaieby
  • , Alena Skálová
  • , Květoslava Michalová
  • , Patrick Schöffski
  • , Andre M. Oliveira
  • , Kevin C. Halling
  • , Sounak Gupta
  • , John M. Gross
  • , Johanna W.M. Nin
  • , Michal Michal
  • , Andrew L. Folpe
  • Kemal Kosemehmetoglu, Jorge Torres-Mora, Michael Michal
  • Charles University
  • Ltd
  • Mayo Clinic Rochester, MN
  • Indiana University Bloomington
  • Maastricht University
  • KU Leuven
  • Chang Gung University
  • Friedrich-Alexander University Erlangen-Nürnberg
  • Aga Khan University
  • Ltd
  • Johns Hopkins University

Araştırma sonucu: Dergiye katkıMakalebilirkişi

15 Alıntılar (Scopus)

Özet

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.

Orijinal dilİngilizce
Makale numarası100337
DergiModern Pathology
Hacim36
Basın numarası12
DOI'lar
Yayın durumuYayınlandı - Ara 2023

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