BenignFibrousDFSP mimicICD-10 L91.0

Keloid scar

Cheloid; keloid scarring; abnormal fibrous scar

Keloid is a benign but disfiguring fibroproliferative scar that extends beyond the original wound margin — distinguishing it from a hypertrophic scar, which respects the original wound. It is far commoner and more severe in Fitzpatrick IV–VI skin (genetic predisposition; 5–15× higher prevalence than Fitzpatrick I–III). Earlobes, presternal chest, upper back, deltoid and posterior neck are predilection sites. A long-standing rapidly enlarging keloid is occasionally biopsied as suspected dermatofibrosarcoma protuberans — the major skin-oncology differential. Treatment is multimodal — intralesional steroid + 5-fluorouracil, silicone, cryotherapy, surgical excision with adjuvant radiotherapy. Recurrence is the norm; setting expectations is essential.

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

Clinical features

  • Firm, raised, shiny, pink-violet to brown scar extending beyond the original wound or injury margin.
  • Onset weeks to years after initial wound (acne, piercing, surgery, vaccination, trauma).
  • Pruritus and pain common; spontaneous regression is rare.
  • Common sites — earlobes (piercings), presternum, upper back / shoulder (acne), deltoid, posterior neck. Mid-face / scalp / eyelids rarely affected.
  • Fitzpatrick IV–VI substantially over-represented; family history strong.

Hypertrophic scar vs keloid vs DFSP

  • Hypertrophic scar — confined to the original wound margin; often regresses over 1–2 years; less symptomatic.
  • Keloid — extends beyond the original wound; persistent; bothersome.
  • DFSP — primary indolent mesenchymal tumour; nodules within an indurated scar-like plaque; often on trunk; CD34+, COL1A1-PDGFB fusion. Biopsy any keloid that becomes nodular, rapidly enlarges, or develops in an atypical site.
  • Lobomycosis, dermatofibroma, hypertrophic lichen planus, keloid acne — other DDx in selected contexts.

Management

  • Multimodal combination is more effective than monotherapy. Common combinations:
    • Intralesional triamcinolone 10–40 mg/mL every 4–6 weeks for 3–6 cycles.
    • Intralesional 5-fluorouracil 50 mg/mL (alone or mixed with triamcinolone 90:10 ratio) — improved efficacy with reduced steroid atrophy.
    • Silicone sheets / gel — daily for ≥ 12 hours, for at least 3 months.
    • Pressure therapy — particularly for earlobe keloids (pressure earring).
    • Cryotherapy — intralesional or surface; reduces volume.
    • Surgical excision — only when combined with adjuvant intralesional triamcinolone + 5-FU or with adjuvant radiotherapy (single dose 12 Gy within 24 hours). Recurrence without adjuvant is > 50%.
    • Laser — pulsed dye laser for erythema; fractional ablative laser for texture.
  • Persistent / recurrent keloid — refractory; combination IL-bleomycin, imiquimod 5% post-excision, or specialist scar service.
  • Counselling — set realistic expectations: improvement, not necessarily resolution; recurrence common; ongoing maintenance.

Prevention in at-risk patients

  • Avoid elective surgery / piercings on high-risk sites (presternum, deltoid, earlobe) in keloid-prone patients.
  • Optimise wound healing — tension-free closure, layered closure, antiseptic care, infection prevention.
  • Silicone sheet / gel prophylactically on healing wounds for 3 months.
  • Post-surgical pressure therapy for at-risk sites.
  • Steroid injection at suture removal in selected high-risk cases.

References

  1. Mustoe TA et al. International clinical recommendations on scar management. Plast Reconstr Surg; 2002.
  2. Berman B et al. Keloid and hypertrophic scar — review. J Am Acad Dermatol; 2017.
  3. Ogawa R. Keloid and hypertrophic scars — current understanding and treatment. Plast Reconstr Surg; 2010.

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