Clinical Trials Study
Copyright ©The Author(s) 2022.
World J Clin Cases. Jan 7, 2022; 10(1): 166-176
Published online Jan 7, 2022. doi: 10.12998/wjcc.v10.i1.166
Figure 1
Figure 1 Randomization and allocation of patients to the study groups. 5-FU: 5-fluorouracil; TA: triamcinolone.
Figure 2
Figure 2 Representative images of localized chronic eczema lesions before and 2 wk after treatment. Skin lesion of a patient in the intralesional 5-FU+TA treatment group (A) at baseline and (B) 2 wk after 5-FU+TA treatment. Skin lesion of a patient in the intralesional TA treatment group (C) at baseline and (D) 2 wk after TA treatment. 5-FU: 5-fluorouracil; TA: triamcinolone.
Figure 3
Figure 3 Clinical responses of the localized lesions of chronic eczema to intralesional treatment with low-dose 5-FU+TA and TA at 2 wk after treatment. (A) Mean atopic dermatitis severity index (ADSI) scores before and 2 wk after treatment. (B) A number of patients who achieved cure, excellent response, and good response 2 wk after treatment with 5-FU+TA or TA. (C) A number of patients who experienced relapse after treatment with 5-FU+TA (n = 4) or TA (n = 25) during 1-year follow-up. (bP < 0.01). 5-FU: 5-fluorouracil; TA: triamcinolone.
Figure 4
Figure 4  Histopathology and immunohistochemistry of localized lesions of chronic eczema to intralesional treatment with 5-FU+TA and TA before and 2 wk after treatment. (A) Representative histologic images of biopsy specimens from localized lesions of chronic eczema were collected before and at 2 wk after treatment. Tissue samples (n = 15 for each group) were stained with HE and antibodies against CD4, CD8, or CD103 to detect T-cell infiltration in the lesional skin. (B) CD4+, CD8+, and CD103+ T cell counts were quantified in high-power field images of lesions biopsied before and 2 wk after treatment. Blue points: 5-FU + TA group; Red points: TA group. aP < 0.05, bP < 0.01. 5-FU, 5-fluorouracil; TA, triamcinolone.