Whorling cellular perineurioma: A previously undescribed variant closely mimicking monophasic fibrous synovial

Michael Michal1, Dmitry V Kazakov2, Abbas Agaimy3

  • 1Department of Pathology, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 80, 304 60 Pilsen, Czech Republic; Biomedical Center of the Faculty of Medicine in Pilsen, Alej Svobody 80, 304 60 Pilsen, Czech Republic.

Insights

A new perineurioma (PN) variant, termed "whorling cellular perineurioma," mimics monophasic fibrous synovial sarcoma (MSS). This distinctive PN subtype exhibits bland morphology and perineurial features, aiding in crucial differential diagnosis.

Area of Science:

  • Surgical Pathology
  • Oncology
  • Dermatopathology

Background:

  • Perineurioma (PN) is a nerve sheath tumor.
  • A rare variant of PN can mimic other soft tissue tumors.
  • Distinguishing PN variants from mimics is critical for accurate diagnosis and patient management.

Purpose of the Study:

  • To describe a distinctive perineurioma variant.
  • To highlight its morphological resemblance to monophasic fibrous synovial sarcoma (MSS).
  • To propose a new term and emphasize diagnostic considerations.

Main Methods:

  • Morphological analysis of four tumors.
  • Immunohistochemical staining for EMA, Claudin-1, GLUT-1, S100 protein, CD34, OSCAR, CK7, and TLE-1.
  • Fluorescence in situ hybridization (FISH) for SYT gene.
  • Electron microscopy in one case.

Main Results:

  • Tumors showed monotonous, densely cellular whorls/sheets with perineurial differentiation.
  • Immunohistochemistry was positive for EMA, Claudin-1, GLUT-1 and negative for S100, CD34, OSCAR, CK7, TLE-1.
  • FISH for SYT gene was negative; electron microscopy confirmed perineurial features. Ki-67 was low (1-3%).

Conclusions:

  • A novel, highly cellular perineurioma variant is described, termed "whorling cellular perineurioma."
  • This entity morphologically resembles monophasic fibrous synovial sarcoma but has distinct immunohistochemical and genetic profiles.
  • Recognition of this variant is crucial for differentiating it from synovial sarcoma, ensuring appropriate clinical management.

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