# Successful Use of Dupilumab in the Treatment of Acquired Perforating Dermatosis Associated with Atopic Dermatitis

**Authors:** Niccolò Gori, Eleonora De Luca, Andrea Chiricozzi, Stefania Sfregola, Alessandro Di Stefani, Ketty Peris

PMC · DOI: 10.1155/2024/6265608 · Case Reports in Dermatological Medicine · 2024-06-19

## TL;DR

A patient with a rare skin condition linked to atopic dermatitis was successfully treated with dupilumab after conventional treatments failed.

## Contribution

This case report demonstrates the novel use of dupilumab to treat acquired perforating collagenosis associated with atopic dermatitis.

## Key findings

- Dupilumab led to complete resolution of clinical signs and symptoms in a patient resistant to conventional treatments.
- Chronic pruritus from atopic dermatitis likely contributed to the development of acquired perforating collagenosis.
- Dupilumab's inhibition of IL-4 and IL-13 signaling may be effective for type 2-driven pruritic dermatoses.

## Abstract

Acquired reactive perforating collagenosis is a rare cutaneous disorder characterised by the extrusion of abnormal connective tissue trough epidermidis and/or follicular units. Reactive perforating collagenosis is often associated with systemic diseases in which pruritus is a common symptom (e.g., diabetes and chronic kidney disease). Less commonly, it has been associated with chronic inflammatory dermatoses, including atopic dermatitis, as in this case. In this report, we describe the exceptional case of a 35-year-old man affected by acquired reactive perforating collagenosis associated with atopic dermatitis who was resistant to conventional topical and systemic treatment and experienced complete resolution of clinical signs and symptoms after 12 weeks of treatment with dupilumab. In our patient, the severe pruritus induced by atopic dermatitis likely contributed to the development of acquired perforating collagenosis lesions, which are thought to be a reactive response to chronic scratching and repetitive injury to the skin. Chronic pruritus in atopic dermatitis is known to be driven by type 2 cytokines, including IL-4 and IL-13, and dupilumab, a monoclonal antibody inhibiting IL-4 and IL-13 signalling, has been shown to be effective in the treatment of moderate to severe atopic dermatitis as well as other type 2-driven pruritic dermatological conditions. This case supports the potential use of dupilumab for the treatment of reactive perforating dermatosis.

## Linked entities

- **Diseases:** atopic dermatitis (MONDO:0004980), diabetes (MONDO:0005015), chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}
- **Diseases:** cutaneous disorder (MESH:D018366), Perforating Dermatosis (MESH:D012871), diabetes (MESH:D003920), Acquired reactive perforating collagenosis (MESH:C565687), Chronic pruritus (MESH:D011537), Atopic Dermatitis (MESH:D003876), pruritic dermatological conditions (MESH:D000168), systemic diseases (MESH:D034721), chronic kidney disease (MESH:D051436)
- **Chemicals:** Dupilumab (MESH:C582203)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11208807/full.md

## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC11208807/full.md

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Source: https://tomesphere.com/paper/PMC11208807