Cutaneous syncytial myoepithelioma with folliculocentric growth and EWSR1 gene rearrangement: A case report

Author:

Nagayasu Mayumi Akaki12ORCID,Tanaka Hiroyuki3,Nogami Kyoko4,Kukita Yoji5,Nakamura Harumi5,Motoi Toru6,Manabe Toshiaki7,Kataoka Hiroaki2

Affiliation:

1. Clinical Laboratory University of Miyazaki Hospital Miyazaki Japan

2. Section of Oncopathology and Regenerative Biology, Department of Pathology, Faculty of Medicine University of Miyazaki Miyazaki Japan

3. Department of Diagnostic Pathology University of Miyazaki Hospital Miyazaki Japan

4. Department of Dermatology University of Miyazaki Hospital Miyazaki Japan

5. Laboratory of Genomic Pathology Osaka International Cancer Institute Osaka Japan

6. Department of Pathology Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital Tokyo Japan

7. Sakaimachi‐Oike Pathology Clinic Kyoto Japan

Abstract

AbstractCutaneous syncytial myoepithelioma is a tumor type that was initially reported in 2013 as a syncytial variant of cutaneous myoepithelioma characterized by intradermal nodular proliferation of oval to spindle‐shaped tumor cells in solid and syncytial patterns. Fusion of genes Ewing sarcoma breakpoint region 1 / EWS RNA binding protein 1 (EWSR1) and pre‐B cell leukemia homeobox 3 (PBX3) is found in approximately 90% of the cases. We report a case of cutaneous syncytial myoepithelioma with diagnostic difficulty due to folliculocentric morphology and atypical immunohistochemical results, including diffuse positivity of α‐smooth muscle actin and claudin 4 and negative immunoreactions for epithelial membrane antigen and S100 protein. In the present case, fluorescence in situ hybridization study demonstrated EWSR1 rearrangement. We further provide a discussion of differential diagnoses with a review of relevant literature.

Publisher

Wiley

Subject

Dermatology,Histology,Pathology and Forensic Medicine

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