A Case Report of an Unusual Presentation of Plexiform Epithelioid Schwannoma
Fatima S Almohannadi, Rami A Mesk, Omar M Braizat, Mohamed B Ahmed, Abeer Alsherawi

TL;DR
A 46-year-old man had a rare benign tumor on his chin diagnosed as plexiform epithelioid schwannoma after surgery and testing.
Contribution
This case report adds to the limited literature on plexiform epithelioid schwannoma with a unique clinical presentation.
Findings
The tumor was confirmed as plexiform epithelioid schwannoma through histopathology and immunohistochemistry.
The patient showed no signs of recurrence after surgical excision.
S-100 and SOX10 markers were strongly positive, supporting the diagnosis.
Abstract
Plexiform epithelioid schwannoma (PES) is a rare, benign nerve sheath tumor that can resemble malignant tumors, making diagnosis challenging. We present the case of a 46-year-old Filipino man with a slow-growing mass on his chin. After surgical excision, histopathology confirmed it as PES. Immunohistochemistry supported the diagnosis, showing strong S-100 and SOX10 positivity. The patient recovered well, with no signs of local recurrence. This case highlights the importance of thorough pathological evaluation when diagnosing rare tumors like PES.
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Click any figure to enlarge with its caption.
Figure 1
Figure 2
Figure 3Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsNeurofibromatosis and Schwannoma Cases · Meningioma and schwannoma management · Soft tissue tumors and treatment
