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Primary Alveolar Soft Part Sarcoma of Cheek: Report of a Case and Review of the Literature.

Katsutoshi HiroseKohei NaniwaYu UsamiMasaharu KoharaToshihiro UchihashiSusumu TanakaSaori YamadaYuri IwamotoShumei MurakamiKaori OyaYasuo FukudaYumiko HoriEiichi MoriiSatoru Toyosawa
Published in: Head and neck pathology (2021)
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.
Keyphrases
  • poor prognosis
  • induced apoptosis
  • rare case
  • genome wide
  • cell cycle arrest
  • copy number
  • chronic pain
  • oxidative stress
  • signaling pathway
  • endoplasmic reticulum stress
  • cell proliferation
  • dna methylation
  • gene expression