| Literature DB >> 33840045 |
Katsutoshi Hirose1, Kohei Naniwa1, Yu Usami1, Masaharu Kohara2, Toshihiro Uchihashi3,4, Susumu Tanaka3, Saori Yamada3, Yuri Iwamoto5, Shumei Murakami5, Kaori Oya6, Yasuo Fukuda6, Yumiko Hori2, Eiichi Morii2, Satoru Toyosawa7.
Abstract
Alveolar soft part sarcoma (ASPS) is a rare soft tissue sarcoma characterized by an alveolar or organoid arrangement of polygonal tumour cells separated by fibrovascular septa. A specific fusion gene [ASPS critical region 1 (ASPSCR1)-TFE3] was detected in ASPS. Despite being a slow-growing tumour without pain and dysfunction, ASPS is characterized by early metastasis, which leads to poor prognosis. Herein, we report a rare case of primary ASPS of the cheek harbouring ASPSCR1 (exon 7)-TFE3 (exon 5) fusion gene in a 21 year-old woman. This tumour was a well-circumscribed, smooth, round mass that was clinically suspected as a benign tumour. However, histologically, it was observed that the polygonal tumour cells were arranged in solid and alveolar growth patterns. Post-operative examination of the whole body excluded the possibility of metastasis at other sites. Thus, careful immunohistochemical and genetic analyses, as well as whole-body examination, demonstrated that the tumour was a primary ASPS of the cheek.Entities:
Keywords: ASPS; ASPSCR1; Alveolar soft part sarcoma; Cheek tumour; TFE3
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Year: 2021 PMID: 33840045 PMCID: PMC8633199 DOI: 10.1007/s12105-021-01324-6
Source DB: PubMed Journal: Head Neck Pathol ISSN: 1936-055X