Mucin‐poor follicular mycosis fungoides

    Mustafa Abdullah Özdemir, Cüyan Demirkesen, Nurcan Arzuhal, Yalçýn Tüzün
    TLDR The patient's symptoms improved with treatment but recurred when the steroid dose was reduced, requiring ongoing therapy.
    A 49-year-old woman with a 4-year history of generalized pruritus developed symptoms including erythema, alopecia totalis, and follicular hyperkeratoses. Histological examination revealed folliculocentric infiltration by atypical T-cells, primarily CD3(+) and CD4(+), with minimal mucin presence. Initial treatment with PUVA led to partial symptom improvement, while subsequent oral methyl prednisolone further alleviated symptoms and normalized beta 2 microglobulin levels. However, symptoms recurred after reducing the steroid dose, necessitating increased steroid dosage and resumption of PUVA therapy. The patient continued to receive both treatments, with follicular papules observed on the upper extremities.
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