Melanocytic Panfolliculoma: A Case Report of a Rare Benign Follicular Tumor

Allie Preston1, Cameron West2, Martha McCollough3

  • 1Department of Dermatology, Baylor Scott & White, Temple, TX.

Insights

A rare pigmented panfolliculoma (PF) on sun-damaged skin mimicked malignancy. This benign follicular tumor showed differentiation and heavy pigmentation, leading to a proposed new designation: melanocytic PF.

Area of Science:

  • Dermatopathology
  • Oncology
  • Hair Follicle Biology

Background:

  • Panfolliculomas (PF) are rare, benign neoplasms originating from hair follicle structures.
  • Several variants of PF have been documented, highlighting their diverse histopathological presentations.
  • Benign follicular tumors can sometimes present with clinical features that mimic malignant neoplasms.

Observation:

  • A case study of an 83-year-old male with a pigmented lesion on actinically damaged skin is presented.
  • The lesion was clinically suspicious for malignancy, necessitating thorough histopathological examination.
  • Histological analysis revealed a tumor with features of infundibular, outer root sheath, and matrical differentiation.

Findings:

  • The tumor exhibited significant melanin pigmentation and an increased number of melanocytes.
  • These findings suggest a dual differentiation pathway involving both follicular and melanocytic components.
  • The tumor was diagnosed as a rare pigmented variant of panfolliculoma.

Implications:

  • The proposed designation 'melanocytic panfolliculoma' accurately reflects the observed histopathological features.
  • This case expands the spectrum of known panfolliculoma variants.
  • Recognizing this variant is crucial for accurate diagnosis and appropriate clinical management, distinguishing it from cutaneous malignancies.