# Verruciform Xanthoma Within the Cyst Lining of Hidradenitis Suppurativa

**Authors:** Deaquan Nichols, Aref Moshayedi, Ja Hea Gu, David M. Milgraum, Mark C. Mochel

PMC · DOI: 10.1111/cup.70042 · Journal of Cutaneous Pathology · 2025-12-16

## TL;DR

A rare skin lesion called verruciform xanthoma was found within a cyst in a patient with hidradenitis suppurativa, suggesting chronic inflammation may cause such changes.

## Contribution

This is the first reported case of verruciform xanthoma occurring in the context of hidradenitis suppurativa.

## Key findings

- VX-like changes were identified in 10% of a follicular cyst lining in a patient with HS.
- Chronic inflammation, rather than genetic factors, is suggested as the cause of the VX-like changes.
- The finding helps distinguish VX from squamous cell carcinoma in chronic inflammatory dermatoses.

## Abstract

Verruciform xanthoma (VX) is a rare lesion most often seen in the oral mucosa or anogenital region, most commonly characterized histologically by verrucous epithelial hyperplasia and foamy histiocytes in the papillary dermis. While VX has been reported in association with inflammatory dermatoses such as lichen planus and lichen sclerosus, its occurrence in the context of hidradenitis suppurativa (HS) has not been previously documented. In this case we present a 56‐year‐old man with long‐standing, Hurley Stage 3 HS affecting the gluteal region. Following surgical excision of a draining sinus tract, histopathology revealed a squamous‐lined follicular cyst consistent with HS, with approximately 10% of the cyst lining displaying features characteristic of VX, including papillomatous acanthosis, parakeratosis with neutrophils, and underlying foamy macrophages. Retrospective review of prior HS specimens did not show similar changes. This case expands the histologic spectrum of HS and suggests that chronic inflammation may promote secondary verruciform xanthomatous changes within follicular cysts. Although mutations in the cholesterol biosynthesis gene NSDHL have been linked to VX, no lichenoid or syndromic features were observed in our patient, supporting an inflammatory rather than genetic etiology. Recognition of VX‐like changes in HS is important to avoid misdiagnosis as squamous cell carcinoma and further elucidates the complex epithelial remodeling in chronic inflammatory dermatoses.

## Linked entities

- **Genes:** NSDHL (NAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL) [NCBI Gene 50814]
- **Diseases:** hidradenitis suppurativa (MONDO:0006559), verruciform xanthoma (MONDO:0003640), lichen planus (MONDO:0006572), lichen sclerosus (MONDO:0007899), squamous cell carcinoma (MONDO:0005096)

## Full-text entities

- **Genes:** NSDHL (NAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL) [NCBI Gene 50814] {aka H105E3, SDR31E1, XAP104}
- **Diseases:** lichen planus (MESH:D008010), lichen sclerosus (MESH:D018459), HS (MESH:D017497), lichenoid (MESH:D017512), chronic (MESH:D002908), squamous cell carcinoma (MESH:D002294), verrucous epithelial hyperplasia (MESH:D017573), Cyst (MESH:D003560), inflammation (MESH:D007249), papillomatous acanthosis (MESH:D058066), inflammatory dermatoses (MESH:D012871), VX (MESH:D014973), follicular cysts (MESH:D005497)
- **Chemicals:** cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC12953008/full.md

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Source: https://tomesphere.com/paper/PMC12953008