The Imaging Appearance of EWSR1::PATZ1 Gene Fusion Central Nervous System Tumors.

Autor: Vanmarcke C; Department of Radiology, UZ Leuven, Leuven, Belgium., Marcelis L; Department of Pathology, UZ Leuven, Leuven, Belgium., Bempt IV; Department of Human Genetics, UZ Leuven and KU Leuven, Leuven, Belgium., Sciot R; Department of Pathology, UZ Leuven and KU Leuven, Leuven, Belgium., Devos J; Department of Radiology, UZ Leuven, Leuven, Belgium.; Department of Imaging & Pathology, Translational MRI, KU Leuven, Leuven, Belgium.
Jazyk: angličtina
Zdroj: Journal of the Belgian Society of Radiology [J Belg Soc Radiol] 2024 Nov 20; Vol. 108 (1), pp. 107. Date of Electronic Publication: 2024 Nov 20 (Print Publication: 2024).
DOI: 10.5334/jbsr.3431
Abstrakt: Ewing Sarcoma Breakpoint Region 1 and POZ/BTB And AT Hook Containing Zinc Finger 1 ( EWSR1::PATZ1 ) gene fusion central nervous system (CNS) tumors are increasingly recognized as a potential distinct entity, with only limited reported cases. The imaging characteristics of these tumors have not been well established. In this study, we provide a detailed radiological description of a case in a 24‑year‑old man and conduct a literature review to identify common imaging features. A total of seven cases, including our own, were evaluated. Histopathological diagnoses included two ependymomas, an infantile glioblastoma, an astroblastoma, a ganglioglioma, and two gliomas not otherwise specified. Common imaging patterns included avid contrast enhancement, intratumoral cysts, intraventricular location or extension leading to hydrocephalus, and sharp delineation. Additional frequently observed features included calcifications and hemorrhagic foci. In conclusion, although the histopathological appearance of EWSR1::PATZ1 gene fusion CNS tumors is diverse, there are consistent imaging features. Recognition of these features can be valuable in the diagnostic process, as radiologists can be the first to suggest the diagnosis.
Competing Interests: The authors have no competing interests to declare.
(Copyright: © 2024 The Author(s).)
Databáze: MEDLINE