Opinion
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Panelists discuss how early-stage CTCL is defined using TNMB staging criteria, the typical presentation of patients at various stages, and the implications for treatment approaches.
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Early-stage mycosis fungoides diagnosis presents significant clinical challenges due to its ability to mimic common benign dermatologic conditions including atopic dermatitis, psoriasis, and other inflammatory skin disorders. The diagnostic process is often prolonged, with patients experiencing delays of 3-7 years before receiving accurate CTCL diagnosis. This delay occurs because early mycosis fungoides lacks specific pathognomonic features that clearly distinguish it from more common skin conditions.
Clinicians should maintain high suspicion for CTCL when skin presentations appear atypical or "bizarre," particularly when lesions show mixed pigmentation patterns, unusual distribution, or fail to respond to standard treatments for presumed benign conditions. The relationship between atopic dermatitis and CTCL is complex, with published data indicating that patients with atopic dermatitis have increased risk of developing CTCL, and CTCL patients showing higher rates of atopic history compared to the general population.
Early stage CTCL definition relies on TNM staging criteria from WHO-EORTC and ISCL guidelines, with early-stage disease characterized by skin-limited involvement presenting as patches or plaques. Stage IA involves less than 10% body surface area, while stage IB encompasses more than 10% involvement. Advanced stage features include tumor formation (thick, elevated lesions) or erythroderma affecting more than 80% of body surface area. Survival outcomes show significant differences between stage IA and more advanced stages, emphasizing the importance of accurate staging for prognosis and treatment planning.