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Short communication Fusion of the FUS and CREB3L2 genes in a supernumerary ring chromosome in low-grade fibromyxoid sarcoma

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TLDR
The genetic findings of a supernumerary ring chromosome from an LGFMS from a 77-year-old man showed that the ring contained material from chromosomes 7 and 16, that the FUS gene was present in two rearranged copies, and that it expressed the F US/CREB3L2 fusion gene.
Abstract
Low-grade fibromyxoid sarcoma (LGFMS) is a rare, low-grade malignant soft tissue tumor that is often mistaken for either benign or more malignant tumor types. Commonly, this tumor affects young adults and typically arises in the deep proximal extremities or trunk with frequent recur- rences and can metastasize to the lungs many years later. Most cases have a recurrent balanced translocation involving chromosomes 7 and 16, t(7;16)(q32-34;p11), which leads to the fusion of the FUS and CREB3L2 genes. However, supernumerary ring chromosomes have been identified in a subset of FUS/CREB3L2-positive LGFMS, but it has not yet been formally demonstrated that such ring chromosomes harbor the FUS/CREB3L2 fusion gene. Here, we report the genetic findings of a supernumerary ring chromosome from an LGFMS from a 77-year-old man. Chromosome banding analysis revealed a supernumerary ring chromosome, and further studies with fluorescence in situ hybridization and reverse transcriptaseepolymerase chain reaction (RT-PCR) showed that the ring contained material from chromosomes 7 and 16, that the FUS gene was present in two rearranged copies, and that it expressed the FUS/CREB3L2 fusion gene. Moreover, an assessment of previously reported cases showed that tumors with ring chromosomes relapsed more often than tumors with a balanced t(7;16), suggesting that ring formation in LGFMS is correlated with tumor

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Journal ArticleDOI

MUC4 is a highly sensitive and specific marker for low-grade fibromyxoid sarcoma.

TL;DR: MUC4 is a highly sensitive and quite specific immunohistochemical marker for LGFMS, and can be helpful to distinguish this tumor type from histologic mimics.
Journal ArticleDOI

Desmoid Tumors: Clinical Features and Treatment Options for Advanced Disease

TL;DR: Treatment options and management strategies for patients with desmoid tumors with a focus on advanced disease are described and watchful waiting may be the most appropriate management in selected asymptomatic patients.
Journal ArticleDOI

MUC4 Is a Highly Sensitive and Specific Marker for Low-Grade Fibromyxoid Sarcoma

TL;DR: MUC4 is a highly sensitive and quite specific immunohistochemical marker for LGFMS, and can be helpful to distinguish this tumor type from histologic mimics.
Journal ArticleDOI

FUS-CREB3L2/L1-Positive Sarcomas Show a Specific Gene Expression Profile with Upregulation of CD24 and FOXL1.

TL;DR: The gene expression profile of LGFMS is distinct from that of soft tissue tumors with similar morphology, and MUC4 was identified as a potential diagnostic marker forLGFMS by gene expression and IHC analysis.
Journal ArticleDOI

Low-grade fibromyxoid sarcoma: Clinical, morphologic and genetic features

TL;DR: A potential relationship between LGFMS and sclerosing epithelioid fibrosarcoma (SEF), a rare fibroblastic neoplasm that most commonly arises in the deep soft tissues of the lower extremities, limb girdles or trunk, has been suggested and is reviewed.
References
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ISCN 2009 - An International System for Human Cytogenetic Nomenclature

TL;DR: ISCN 2009 - An International System for Human Cytogenetic Nomenclature - Libros de Medicina - Genetica - 28,97
Journal ArticleDOI

Low-grade Fibromyxoid Sarcoma. A Report of Two Metastasizing Neoplasms Having a Deceptively Benign Appearance

TL;DR: Two deceptively benign-appearing, unclassifiable but very similar fibromyxoid sarcomas characterized histologically by bland, innocuous-appearance fibroblastic cells and a swirling, whorled growth pattern are presented.
Journal ArticleDOI

Low-grade fibromyxoid sarcoma: a clinicopathologic study of 33 cases with long-term follow-up.

TL;DR: The most common tumor locations were the shoulder area (5), thigh (5, and inguinal area (4) as discussed by the authors, where the tumor size varied from 1.5 to 16 cm (median, 9.4 cm) in those cases in which it was known.
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