Keratoacanthoma ICD-10: L85.8
Often searched as: bump on face that grew fast, skin lump with hole in center, fast growing skin nodule, dome shaped bump on face, crater in skin bump, growth on face that appeared quickly, wart like growth on hands or face, sun damage bump skin…
Clinical urgency level
Systems Affected
Severity Levels
mild
Classic keratoacanthoma on a low-risk site (arm, trunk) following typical rapid growth and spontaneous regression cycle — can be monitored with close follow-up.
moderate
Large or persistent keratoacanthoma on the face, nose, or ear not showing signs of regression — surgical removal recommended to prevent disfigurement.
severe
Locally aggressive variant, perineural invasion, or keratoacanthoma centrifugum marginatum (rapidly expanding peripheral type) — requires urgent wide excision and histologic confirmation to rule out SCC.
Red Flags
- A bump that grows very rapidly over 4–8 weeks to 1–2cm (distinguishing feature of KA)
- Lesion on the face, nose, lip, or ear where local tissue destruction can cause disfigurement
- Lesion not regressing after 3–4 months as expected
- Ulceration or bleeding within the lesion
- Multiple keratoacanthomas appearing simultaneously (possible Ferguson-Smith syndrome or Muir-Torre syndrome)
- Lesion in an immunocompromised patient — higher risk of aggressive behavior
Clinical Presentation
Keratoacanthoma — dome-shaped nodule with central keratin-filled crater on the face
Source: Wikimedia Commons (CC BY-SA 3.0 )
Keratoacanthoma image gallery — DermNet NZ
View gallery on DermNet NZ (image gallery reference)When to See a Doctor
See a dermatologist promptly for any rapidly growing skin nodule — especially one with a central plug or crater on the face, hands, or sun-exposed areas. Because keratoacanthoma looks nearly identical to squamous cell carcinoma clinically and histologically, a professional evaluation and often a biopsy are needed to distinguish them. Don't wait to see if it regresses on a cosmetically sensitive area.
Differential Diagnosis
- Squamous cell carcinoma (primary and critical differential — histology needed)
- Basal cell carcinoma (nodular variant)
- Molluscum contagiosum (smaller, central dimple)
- Wart / verruca (rougher surface, slower growth)
- Merkel cell carcinoma (rare — aggressive)
- Dilated pore of Winer (single large open comedone — no keratin plug dome)
Comorbidities
- Chronic UV damage and actinic keratosis
- Muir-Torre syndrome (multiple KAs + sebaceous tumors + internal malignancy — genetic)
- Ferguson-Smith syndrome (multiple self-healing KAs — rare genetic)
- Immunosuppression (organ transplant, HIV — higher risk)
- Prior SCC or other non-melanoma skin cancers
Prognosis
Classic keratoacanthoma is considered benign and often regresses spontaneously within 3–6 months, leaving a depressed scar. However, most dermatologists advocate for surgical removal rather than watchful waiting because: (1) clinical distinction from SCC is unreliable, (2) spontaneous regression leaves a scar regardless, and (3) some lesions are locally aggressive. Surgical excision or Mohs surgery achieves complete cure. Recurrence after removal is uncommon. The rare giant or centrifugum variants may require more aggressive treatment.
Detailed Overview
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