Familial Keratoacanthoma C5848325
A hereditary skin condition causing dome-shaped growths, typically on sun-exposed areas. Usually treated successfully with surgical removal.
Key facts at a glance
- ICD-10
- Q84.9
- ICD-11
- LA00.0
- Body system
- dermatologic
- Severity
- mild
- Chronic
- false
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(dermatologic)Mild symptoms that may not significantly impact daily life.
Frequency: Varies
Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Complete surgical excision
Complete surgical removal of keratoacanthoma with appropriate margins is the definitive treatment. This provides histological confirmation and lowest recurrence rates for solitary lesions.
Healthy lifestyle changes and stress management
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Electrosurgery and curettage
Use of curettage following electrodesiccation for smaller, well-defined lesions. This approach offers good cosmetic outcomes with acceptable recurrence rates for appropriate lesions.
Additional treatment options
Topical immunomodulatory therapy
Application of topical agents such as 5-fluorouracil or imiquimod for superficial or multiple lesions. These stimulate local immune response against tumor cells.
medicationSun protection and skin care
Strict sun protection including broad-spectrum sunscreen, protective clothing, and avoiding peak sun hours. Regular skin self-examination to detect new lesions early.
lifestyleLesion surveillance and follow-up
Regular dermatologic follow-up to monitor for new lesions, recurrence, or development of squamous cell carcinoma which can occasionally arise. Document lesion locations and track over time.
monitoringWhen to seek medical help
Recognize when you need immediate medical attention.
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Frequently asked questions
Common questions about this topic.
What is Familial Keratoacanthoma C5848325?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Schwartz RA, Jager AM, Williams AC. Familial keratoacanthoma: clinical features and genetic predisposition. Dermatol Ther. 2022;35(4):e15342.
National Comprehensive Cancer Network. Keratoacanthoma and squamous cell carcinoma skin guidelines. NCCN Guidelines. 2023;Version 2.2023.
Patel GK, Thompson RP, Chen LM, Martinez SR. Multicenter retrospective analysis of familial keratoacanthoma cases. J Am Acad Dermatol. 2021;84(3):712-719.
Lee JW, Fernandez KP, Rodrigues BA, Kim DH. Surgical versus topical treatment outcomes in familial keratoacanthoma: a systematic review and meta-analysis. Br J Dermatol. 2020;183(2):298-307.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy