Granular Cell (Granular-type) Fibrous Papule of the Face
Case Report and Literature Review Emphasizing Morphologic and Immunohistochemical Pitfalls.
Vance PK, Martin HL
American Journal of DermatopathologyIn the feed 21 Aug 2026, published online 21 Aug 2026, issue 2026 Aug 21, added to PubMed 21 Aug 2026
Topics: Skin cancer & tumorsOther tumors & cystsDermatopathology
Abstract
Granular cell (granular-type) fibrous papule is a rare variant of facial fibrous papule/solitary angiofibroma in which lesional stromal cells show prominent cytoplasmic granularity. Because granular cytoplasm is a nonspecific phenotype shared by tumors of diverse lineage, granular-type fibrous papule may be misdiagnosed as granular cell tumor or other granular-cell lesions. We present a case of granular-type fibrous papule in an adult patient, highlight key histopathologic and immunohistochemical findings, and provide a focused review of published cases. In the literature, reported lesions most often occur on the nose and show periodic acid-Schiff-positive diastase-resistant granules with immunoreactivity for lysosomal markers (eg, CD68, NKI/C3) and absence of schwannian markers (S100/SOX10) in cases where these are documented.
Abstract from PubMed
PMID 42628508 · DOI 10.1097/DAD.0000000000003409