# Dissecting Cellulitis of the Scalp: Linking Pathogenesis to Therapy

**Authors:** Mislav Mokos, Mirna Šitum, Ines Sjerobabski Masnec

PMC · DOI: 10.3390/biomedicines14030570 · Biomedicines · 2026-03-02

## TL;DR

This paper reviews treatment options for dissecting cellulitis of the scalp, focusing on new biologic therapies and their effectiveness in managing severe cases.

## Contribution

The paper provides an updated synthesis of medical and emerging targeted therapies for DCS, emphasizing biologics and small-molecule inhibitors.

## Key findings

- Biologic agents targeting TNF-α, IL-17, and IL-23 show promise for treatment-resistant DCS.
- Systemic retinoids remain first-line therapy, while biologics are increasingly used for moderate-to-severe cases.
- Further controlled studies are needed to optimize treatment sequencing and combinations.

## Abstract

Dissecting cellulitis of the scalp (DCS) is a chronic, inflammatory follicular occlusion disorder characterized by painful nodules, abscesses, and sinus tracts that lead to scarring alopecia. The therapeutic goal is to limit disease progression and the extent of scarring. Although DCS is traditionally managed with systemic retinoids, antibiotics, and surgical interventions, therapeutic responses are variable and long-term remission remains challenging. Recent insights into the immunological overlap between DCS, hidradenitis suppurativa (HS), and other autoinflammatory follicular disorders have expanded therapeutic options, particularly with biologic agents targeting tumor necrosis factor alpha (TNF-α), interleukin (IL)-17, and IL-23 pathways, as well as Janus kinase (JAK) inhibitors. This review synthesizes the current evidence on medical, procedural, and emerging targeted therapies for DCS, incorporating data from case reports, case series, retrospective cohorts, and recent systematic reviews up to 2025. Special emphasis is placed on the evolving role of biologics and small-molecule inhibitors, which show growing promise for refractory or syndromic presentations. Current evidence supports a stepwise, phenotype-driven approach in which systemic retinoids remain first-line systemic therapy, while biologics represent a rational and increasingly evidence-supported option for moderate-to-severe, treatment-resistant, or syndromic disease. Further controlled studies are needed to define optimal sequencing, duration, and combination strategies for long-term management.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), IL17A (interleukin 17A), IL37 (interleukin 37)
- **Chemicals:** antibiotics (PubChem CID 46874763)
- **Diseases:** dissecting cellulitis of the scalp (MONDO:0009848), hidradenitis suppurativa (MONDO:0006559)

## Full-text entities

- **Genes:** IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** Cellulitis of the Scalp (MESH:C562486), autoinflammatory follicular disorders (MESH:D056660), DCS (MESH:C536560), scarring alopecia (MESH:D002921), HS (MESH:D017497), abscesses (MESH:D000038), inflammatory follicular occlusion disorder (MESH:D001157)
- **Chemicals:** retinoids (MESH:D012176)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13023782/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13023782/full.md

## References

129 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023782/full.md

---
Source: https://tomesphere.com/paper/PMC13023782