ProcedureBCC / SKOPCS-4 S09

Curettage and cautery

C&C; curettage and electrodesiccation; ED&C; curettage and electrocautery

Curettage and cautery is a fast, low-cost, scar-tolerable destructive technique for low-risk skin lesions — particularly low-risk basal cell carcinoma on the trunk and proximal extremities, seborrhoeic keratoses requested for cosmesis, and selected actinic keratoses or warts. Carefully selected, BCC C&C has 5-year recurrence rates of 5–10%; poorly selected it can rise to 20% or more. Site, subtype and operator skill are the three determinants of outcome. C&C is not appropriate for any lesion in the H-zone of the face, for morphoeic / infiltrative BCC, recurrent lesions, immunosuppressed patients, or anywhere histology is mandatory.

CurrentLast reviewed 15 May 2026
Clinical image of Curettage and cautery
Curettage and cautery. Image sourced from DermNet New Zealand. Used under CC BY-NC-ND 4.0. No endorsement implied.

Indications

  • Low-risk BCC — nodular or superficial subtype, < 2 cm, on the trunk or proximal extremities, well-circumscribed, primary (not recurrent).
  • Seborrhoeic keratoses for cosmesis after clinical confirmation.
  • Solar lentigines (light pass).
  • Selected hyperkeratotic actinic keratoses.
  • Verruca vulgaris.
  • Always confirm diagnosis clinically (or by prior biopsy) before destructive treatment — C&C destroys the specimen for histology.

Contraindications

  • Any lesion where definitive histology is needed.
  • BCC of the head / neck "H-zone" — central face, periorbital, periauricular, nasal, lip — site associated with elevated recurrence.
  • Morphoeic, infiltrative, micronodular, basosquamous BCC subtypes.
  • Recurrent or incompletely treated BCC.
  • cSCC of any grade — risks under-treatment; use excision.
  • Pigmented lesions where melanoma is possible.
  • Immunosuppressed patients (transplant recipients) — recurrence and progression risk too high.
  • BCC in the setting of Gorlin syndrome — RT exclusion zones, multiplicity make C&C unsuitable.

Technique

  • Mark the lesion with a 2–3 mm cuff of surrounding clinically normal skin.
  • Infiltrate with 1% lidocaine + adrenaline.
  • Firm curettage with a sharp dermal curette (4, 5 or 7 mm) — tumour tissue feels softer ("gritty / butter") than surrounding dermis; this difference guides the depth.
  • Electrodesiccation of the base and a 1–2 mm rim of surrounding normal skin.
  • Repeat curette + cautery cycles (traditionally three) — the "C-E-C-E-C-E" sequence.
  • Haemostasis; dressing.
  • Heal by secondary intention over 2–4 weeks; cosmetic outcome on the trunk usually good; flat or slightly hypopigmented scar.

Outcomes and recurrence

  • BCC 5-year recurrence rate:
    • Low-risk site (trunk) — 5–10% with appropriate selection.
    • High-risk site (head/neck H-zone) — 15–25% — do not use.
    • Recurrent BCC — 40–50% — do not use.
  • Cosmesis is acceptable on most non-facial sites; pigmented scars are common in Fitzpatrick IV–VI skin — counsel about post-inflammatory hyper/hypopigmentation.
  • Histology not generated — incomplete excision cannot be detected; clinical surveillance is essential.

Aftercare and follow-up

  • Daily soap-and-water cleansing; petroleum jelly to maintain moist healing; non-adherent dressing.
  • Avoid sun exposure to the healing wound for 6 months to limit dyschromia.
  • Skin examination at 6 months and annually for 2 years to monitor for recurrence.
  • Counsel on photoprotection and self-examination.

References

  1. Rodriguez-Vigil T et al. Recurrence rates of primary BCC treated by C&C — systematic review. J Am Acad Dermatol; 2007.
  2. Nasr I, McGrath EJ, Harwood CA et al. British Association of Dermatologists guidelines for the management of adults with basal cell carcinoma 2021. Br J Dermatol. 2021;185(5):899-920.

Spot a correction?

If any clinical statement, citation or link on this page needs updating, please email admin@skinoncology.net with the page name, the proposed correction and the supporting source.