Microreticular perineurioma: A new morphological subtype of a rare entity

Haneen T Salah1, Julieta A D'ardis1, Tyler Enos2

  • 1Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.

Insights

A rare microreticular perineuroma, a benign nerve sheath tumor, was identified in an 11-year-old male. This unique variant, presenting as a finger lesion, highlights the importance of recognizing unusual morphologies in peripheral nerve sheath tumors.

Area of Science:

  • Dermatopathology
  • Surgical Pathology
  • Oncology

Background:

  • Perineurioma is a rare, benign peripheral nerve sheath tumor.
  • Known subtypes include plexiform, reticular, and sclerosing variants.
  • The reticular subtype exhibits a characteristic net-like growth pattern.

Observation:

  • An 11-year-old male presented with a slowly enlarging tan-white finger lesion over two years.
  • Microscopic examination revealed a lesion with spindle-shaped cells exhibiting ovoid nuclei and delicate cytoplasmic processes.
  • The cells were arranged in a distinct microreticular pattern.

Findings:

  • The lesional cells demonstrated strong positivity for epithelial membrane antigen (EMA) and claudin-1.
  • The unique microscopic features led to the classification of this case as a microreticular perineuroma.
  • This represents the first reported case of this specific morphologic variant.

Implications:

  • Recognition of microreticular perineuroma is crucial for accurate diagnosis and appropriate patient management.
  • This finding expands the spectrum of known perineuroma subtypes.
  • Complete surgical excision resulted in no recurrence at nine months, suggesting a favorable prognosis for this variant.