Primitive Cutaneous (P)erivascular (E)pithelioid (C)ell Tumour (PEComa): A New Case Report of a Rare Cutaneous Tumor

Genes (Basel). 2022 Jun 26;13(7):1153. doi: 10.3390/genes13071153.

Abstract

Perivascular epithelioid cell tumours (PEComas) are a growing family of tumours composed of histologically and immunohistochemically distinctive perivascular epithelioid cells. Cutaneous primitive PEComas (cPEComas) are very rare, with 65 cases described in the English literature, and occur as a painless lesion predominantly in female patients, with a wide age range. We present a new case of cPEComa found on the left thigh of a 53-year-old patient with histopathological, immunohistochemical, and molecular information. The lesion was positive for HMB-45 and focal for smooth muscle actin and desmin but negative for melan-A, S-100 protein, CD31, and CD34. Next generation sequencing (NGS) analysis demonstrated the presence of genomic aberration for baculoviral IAP repeats containing BIRC3 splice site 1622-27_1631del37. Although there are little molecular data regarding this entity, our case adds to this knowledge, considering the importance of detecting genomic aberrations in the context of specific therapies such as mTOR inhibitors.

Keywords: PEComa; clear cell; cutaneous; mesenchymal; primitive; skin; sugar tumour.

Publication types

  • Case Reports

MeSH terms

  • Epithelioid Cells / chemistry
  • Epithelioid Cells / metabolism
  • Epithelioid Cells / pathology
  • Female
  • Humans
  • Middle Aged
  • Perivascular Epithelioid Cell Neoplasms* / chemistry
  • Perivascular Epithelioid Cell Neoplasms* / metabolism
  • Perivascular Epithelioid Cell Neoplasms* / pathology
  • S100 Proteins
  • Skin Neoplasms* / genetics
  • Skin Neoplasms* / metabolism
  • Transcriptional Elongation Factors

Substances

  • ELL protein, human
  • S100 Proteins
  • Transcriptional Elongation Factors

Grants and funding

This research received no external funding.