Cutaneous SCC in Epidermolysis Bullosa: Closure with DBP

November 19, 20254 min read
Medipyxis Mobile Wound Care Software

Cutaneous SCC in Epidermolysis Bullosa: Primary Wound Closure Using a Decellularized Bovine Pericardium Scaffold

Disclaimer: Educational only; not a substitute for patient‑specific medical advice.

Executive summary (for busy clinicians)

(A patient with epidermis bullosa on their initial visit)

Patient with epidermis bullosa, initial visit

Clinical problem: RDEB patients face aggressive, recurrent cutaneous SCC and closing the oncologic defect is hard—fragile skin, infection risk, and donor‑site morbidity complicate standard options. [1, 2]

Innovation: After wide local excision down to fascia, a decellularized bovine pericardium (DBP) scaffold was used for primary coverage of leg defects in three RDEB patients. The scaffold acted as a biointegrable, temporary ECM, absorbing gradually while supporting epithelialization. [1, 2]

(The same patient after 40 days of treatment)

Progress of wound healing from patient after 40 days

Outcomes: With twice‑weekly applications over ~3 months, each DBP layer degraded over ~10 days, integrated with the wound bed, and all patients achieved full wound healing without staged reconstruction, with fewer dressing changes and improved comfort. [5, 6]

Why it matters: In a niche, high‑risk population where grafts and secondary intention are problematic, DBP enabled reliable, infection‑sparing closure after oncologic surgery. (Case series; n=3.) [5, 6]


Background: Why EB‑related SCC defects are uniquely difficult

Epidermolysis bullosa (EB) causes extreme skin fragility, chronic wounding, and scarring. In its severe recessive dystrophic form (RDEB), patients have a high risk of aggressive mucocutaneous SCC, often requiring surgical excision. Yet closing the post‑excision defect can be more challenging than tumor removal—traditional approaches (secondary intention, autograft, dermal substitutes, keratinocyte suspensions) are hampered by fragile skin, infection risk, and donor‑site morbidity. [1, 2]


How DBP helped where other options struggle

  • Secondary intention can be prolonged and infection‑prone in EB. DBP shortened the path to epithelial cover while minimizing manipulation. [5, 6]

  • Autografts/“autodermoplasty” add donor wounds and can fail in fragile skin; DBP avoids donor‑site morbidity and potential flap/graft rejection scenarios. [5, 6]

  • Artificial dermal substitutes and keratinocyte suspensions remain options, but the series suggests DBP as a cost‑conscious alternative that delivered predictable coverage in these complex cases. (Author‑reported; n=3.) [5, 6]


Practical workflow you can replicate (clinic & OR)

  1. Confirm diagnosis & plan margins. Use punch biopsy to confirm cSCC and map resection margins in RDEB skin. [1, 2]

  1. Excise oncologic tissue with >1 cm margin, down to fascia for a clean, vascularized bed. [3, 4]

  1. Place DBP as a primary scaffold; ensure intimate contact with viable tissue. [5, 6]

  1. Dress gently: silicone mesh + non‑adhesive foam, change q48 h to reduce shear/friction. [9, 10]

  1. Re‑apply DBP twice weekly as needed—each layer absorbs ≈10 days while integrating and supporting epithelialization. [5, 6]

  1. Monitor for closure and signs of infection; in this series, no staged reconstruction was required. [7, 14]


Where this approach fits (and limits)

Best‑fit scenarios

  • RDEB/cSCC defects on the leg where donor‑site creation or prolonged open management is undesirable. [1, 2]

  • Patients at high infection risk or with fragile periwound skin where adhesive trauma must be minimized. [7]

Caveats

  • Evidence level: small case series (n=3); no comparator arm. Findings are practice‑informing, not definitive.

  • Oncologic principles first: margin control and appropriate depth of excision are prerequisites; scaffold does not replace cancer care. [3, 4]


FAQ

What is a decellularized bovine pericardium scaffold?
A biologic matrix derived from bovine pericardium with cellular components removed, leaving a biointegrable ECM scaffold that gradually absorbs while the patient’s tissue re‑epithelializes.
[5, 6]

How often is it applied and how long does it last?
In this series, clinicians applied DBP twice weekly; each application degraded over ≈10 days while integrating into the wound bed.
[5, 6]

Did patients need skin grafts or flaps later?
No—all three achieved full healing without staged reconstruction, which is notable in RDEB.
[1, 2]

What dressings are used on top?
A silicone mesh interface and non‑adhesive foam cover dressing; changed every 48 hours to limit shear.
[9, 10]

How does this compare to other options?
Compared with secondary intention, autografting, or artificial dermal substitutes / keratinocyte suspensions, DBP provided dependable primary coverage without donor‑site morbidity in this small series.
[5, 6]


Bottom line

For RDEB patients undergoing cSCC excision, decellularized bovine pericardium offered primary coverage that integrated, protected, and closed defects—without additional reconstructive stages—while simplifying dressing logistics in extremely fragile skin. Consider this approach when graft morbidity or prolonged secondary intention would be especially risky. [1, 2]


References

[1] Fine JD. Life‑threatening cSCC in RDEB. J Am Acad Dermatol, 2009. — https://pubmed.ncbi.nlm.nih.gov/19026465/

[2] Harries C, et al. Aggressive behaviour of cSCC in RDEB‑severe. Br J Dermatol, 2022. — https://academic.oup.com/bjd/article/187/5/824/6966416

[3] AAD Guidelines of care for management of cutaneous SCC, 2018. — https://pmc.ncbi.nlm.nih.gov/articles/PMC6652228/

[4] Nahhas AF, et al. Review of global guidelines on cSCC surgical margins. 2017. — https://pmc.ncbi.nlm.nih.gov/articles/PMC5404779/

[5] Solarte‑David VA, et al. Decellularized tissues for wound healing (review). Front Bioeng Biotech, 2022. — https://www.frontiersin.org/articles/10.3389/fbioe.2022.821852/full

[6] Di Francesco D, et al. Hydrogel from decellularized bovine pericardium ECM (characterization). Front Bioeng Biotech, 2024. — https://www.frontiersin.org/articles/10.3389/fbioe.2024.1452965/full

[7] Alizadeh S, et al. Bilayer antibacterial dressing from decellularized bovine pericardium (materials study). 2024. — https://www.sciencedirect.com/science/article/abs/pii/S0141813024078644

[9] Wounds International. Soft silicone dressings — Made Easy. 2012. — https://woundsinternational.com/wp-content/uploads/2023/02/c6c17c8108884b42545f060eabc1d29f.pdf

[10] DermNet. Silicone dressings overview (atraumatic contact layers). — https://dermnetnz.org/topics/silicone-dressings

[11] Pope E, et al. A consensus approach to wound care in epidermolysis bullosa. 2012. — https://pmc.ncbi.nlm.nih.gov/articles/PMC3655403/

[12] Pabón‑Carrasco M, et al. EB wound care management—atraumatic dressings recommended. Healthcare (Basel), 2024. — https://www.mdpi.com/2227-9032/12/2/261

[14] Ann Plast Surg 2009. Cadaveric allograft for wound closure after SCC resection in RDEB (case series). — https://journals.lww.com/annalsplasticsurgery/abstract/2009/09000/cadaveric_allograft_for_wound_closure_after.15.aspx

Medipyxis Mobile Wound Care Software

Back to Blog