# Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review

**Authors:** Pratiksha Patra, Sairekha Ravichandran, Nishit Patel, Paul Rodriguez-Waitkus, Wei-Shen Chen

PMC · DOI: 10.7759/cureus.98811 · Cureus · 2025-12-09

## TL;DR

This case report describes scarring hair loss in a patient with localized dystrophic epidermolysis bullosa, highlighting its similarity to a skin condition called lichen planopilaris.

## Contribution

The paper presents a rare case of scarring alopecia in localized dystrophic epidermolysis bullosa and emphasizes its clinical and histological features.

## Key findings

- The patient showed hair thinning and fibrosis around hair follicles consistent with scarring alopecia.
- Histology revealed features overlapping with dystrophic epidermolysis bullosa and lichen planopilaris.
- The case underscores the need to consider inflammatory causes alongside EB-related alopecia.

## Abstract

Alopecia is a recognized complication of the epidermolysis bullosa (EB) group of blistering diseases, with diffuse and scarring alopecia seen in severe generalized EB. However, there is a dearth of literature characterizing alopecia in localized EB, with few reports of scarring and non-scarring alopecia in dystrophic EB (DEB).

In this report, we present a case of a 58-year-old female with an eight-year history of pretibial DEB and a documented heterozygous COL7A1 mutation, who presented to the dermatology clinic with improving skin fragility after five months of topical beremagene geperpavec therapy, now noting gradual hair thinning on the vertex scalp over one year. Clinical examination revealed decreased hair density on the vertex and frontal scalp, with scattered sclerotic papules, without significant perifollicular scale or erythema. Two punch biopsies were obtained for histologic vertical and horizontal sections, revealing superficial and mid-dermal fibrosis encircling hair follicles at the infundibulum and isthmus, numerous fibrous stelae, a superficial perifollicular lymphocytic infiltrate with scattered follicular dyskeratotic keratinocytes, and preservation of sebaceous glands. Together, these findings were consistent with scarring alopecia with shared features of DEB and lichen planopilaris (LPP). We highlight the importance of recognizing scarring alopecia as a complication of DEB, with discernment for concomitant inflammatory etiologies that may co-occur, especially in a patient with a COL7A1 mutation.

## Linked entities

- **Genes:** COL7A1 (collagen type VII alpha 1 chain) [NCBI Gene 1294]
- **Diseases:** epidermolysis bullosa (MONDO:0006541), lichen planopilaris (MONDO:0018879)

## Full-text entities

- **Genes:** COL7A1 (collagen type VII alpha 1 chain) [NCBI Gene 1294] {aka EBD1, EBDCT, EBR1, NDNC8}
- **Diseases:** DEB (MESH:D016108), LPP (MESH:D008010), blistering diseases (MESH:D001768), Scarring Alopecia (MESH:D002921), EB (MESH:D004820), skin fragility (MESH:C536183), fibrosis (MESH:D005355), inflammatory (MESH:D007249), erythema (MESH:D004890), Alopecia (MESH:D000505)
- **Chemicals:** beremagene geperpavec (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12782298/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12782298/full.md

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Source: https://tomesphere.com/paper/PMC12782298