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Keratoacanthoma: Update on the Debate.
Alexander Nirenberg1, Howard Steinman2,3, Anthony Dixon1,4
1Australasian College of Cutaneous Oncology, Docklands, VIC, Australia.
The American Journal of Dermatopathology
|January 4, 2021
Summary
Keratoacanthoma (KA), a skin tumor, grows rapidly then involutes, often on sun-damaged skin. While debated, KA may be a low-grade squamous cell carcinoma variant with distinct genetic differences.
Area of Science:
- Dermatology
- Oncology
- Pathology
Background:
- Keratoacanthoma (KA) is a common cutaneous tumor characterized by rapid growth followed by spontaneous involution.
- KA typically affects sun-exposed skin and has numerous potential causative associations, including certain therapeutic agents.
- The classification of KA remains contentious, with ongoing debate regarding its relationship to squamous cell carcinoma (SCC).
Purpose of the Study:
- To review the current understanding of Keratoacanthoma (KA) and its relationship with Squamous Cell Carcinoma (SCC).
- To explore the reasons for inconsistent reporting and diagnosis between KA and SCC.
- To highlight genetic and pathogenetic differences and similarities between KA and SCC.
Main Methods:
- Review of existing literature on Keratoacanthoma (KA) and Squamous Cell Carcinoma (SCC).
- Analysis of microscopic criteria and clinical behavior of KA.
- Examination of genetic studies and pathogenetic factors, including apoptotic pathways and viral involvement.
Main Results:
- Inconsistent reporting of KA versus SCC is attributed to overlapping microscopic features, aggressive KA variants, and potential medicolegal factors.
- Genetic studies reveal distinctions between KA and SCC, with evidence of activated apoptotic pathways in KA.
- Human polyomavirus 6 is implicated in the pathogenesis of some KA cases.
Conclusions:
- Keratoacanthoma (KA) can be considered a low-grade variant of Squamous Cell Carcinoma (SCC) due to overlapping features and some shared genetic underpinnings.
- Despite similarities, distinct genetic differences and pathogenetic factors support a nuanced classification.
- Accurate differentiation between KA and SCC is crucial for appropriate patient management and treatment strategies.
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