Relation Between Atypical Fibroxanthoma and Pleomorphic Dermal Sarcoma: Histopathologic Features and Review of the Literature

Actas Dermosifiliogr (Engl Ed). 2021 May;112(5):392-405. doi: 10.1016/j.ad.2020.11.018. Epub 2020 Dec 7.
[Article in English, Spanish]

Abstract

The relation between atypical fibroxanthoma and pleomorphic dermal sarcoma has led to confusion and debate in the literature. Both tumors present on sun-exposed skin, typically on the head and neck, in patients of advanced age. Both are comprised of a variable mix of histiocytoid, spindle, epithelioid, and/or giant multinucleated cells with pleomorphic nuclei. No immunohistochemical diagnostic techniques have emerged to distinguish these tumors. Diagnosis is by exclusion. Histologically, atypical fibroxanthoma is seen as a well-circumscribed dermal nodule but there will be no evidence of extensive subcutaneous invasion, tumor necrosis, or lymphovascular or perineural invasion. Therefore, if any of the aforementioned features is present, the diagnosis would be pleomorphic dermal sarcoma. This narrative review of the literature aims to identify the distinguishing and overlapping histopathologic features of these 2 tumors as they have been described in case series.

Keywords: Atypical fibroxanthoma; Fibroxantoma atípico; Histopathologic relationship; Pleomorphic dermal sarcoma; Relación histopatológica; Review; Revisión; Sarcoma pleomórfico dérmico.

Publication types

  • Review

MeSH terms

  • Diagnosis, Differential
  • Humans
  • Sarcoma* / diagnosis
  • Skin Neoplasms* / diagnosis