| Literature DB >> 28601660 |
Satoshi Kuwamoto1, Michiko Matsushita2, Kenichi Takeda3, Natsumi Tanaka3, Yukari Endo4, Akira Yamasaki3, Kenichi Kohashi5, Yoshinao Oda5, Yasushi Horie4.
Abstract
SMARCA4-deficient thoracic sarcoma is a recently proposed new entity of soft tissue sarcomas with an undifferentiated round cell morphology that is diagnostically challenging. Here we report a case of this tumor where the diagnosis was established using limited samples and resources. A woman in her early 30s developed two intrathoracic masses. Biopsies for these lesions showed sheets of undifferentiated round/rhabdoid cells that retained SMARCB1 expression. Further analysis revealed a reduced SMARCA4 expression and a complete loss of SMARCA2 expression in tumor cells. Subsequent Sanger sequencing identified a nonsense c.1546A>T (p.516Lys>Ter) mutation in SMARCA4 and confirmed the diagnosis. Our case highlighted clinicopathological correlation and rational use of tissue sections for immunohistochemistry may enable to diagnose this tumor even when only limited samples are available. Recognition of this new entity is important for further understanding of the disease and the future development of specific therapies.Entities:
Keywords: Immunohistochemistry; Mutation analysis; Rhabdoid cells; SMARCA4-deficient thoracic sarcoma; SWI/SNF complex
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Year: 2017 PMID: 28601660 DOI: 10.1016/j.humpath.2017.05.024
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466