Mycosis fungoides with a CD56+ immunophenotype

被引:37
作者
Wain, EM
Orchard, GE
Mayou, S
Atherton, DJ
Misch, KJ
Russell-Jones, R
机构
[1] St Thomas Hosp, St Johns Inst Dermatol, Skin Tumor Unit, London SE1 7EH, England
[2] St Thomas Hosp, St Johns Inst Dermatol, Dept Dermatopathol, London SE1 7EH, England
[3] Chelsea & Westminster Hosp, Dept Dermatol, London, England
[4] Great Ormond St Hosp Sick Children, London WC1N 3JH, England
[5] Kingston Hosp, Kingston upon Thames, Surrey, England
关键词
D O I
10.1016/j.jaad.2005.01.133
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
We report 3 cases of mycosis fungoides (MF) with a CD56(+) cytotoxic immunophenotype. Each patient presented with a different clinical phenotype: one exhibited limited poikilodermatous patches (skin stage T1); one, widespread hypopigmented lesions (skin stage T2); and one, poikiloderma with a single cutaneous tumor (skin stage T3). MF was confirmed both histologically and by the presence of a T-cell receptor clone in lesional skin in all cases. CD56 and T-cell intracellular antigen-1 were expressed by the malignant lymphocytes in all patients and two expressed CD8. No sample demonstrated loss of the pan T-cell markers CD2 or CD3. None of the 3 developed systemic disease and T-cell receptor gene analysis of peripheral blood was polyclonal in all cases. Only 3 cases of CD56(+) MF have been reported previously, none of which exhibited tumor-stage disease. Currently, the disease in our patients appears to be behaving in a manner similar to that predicted for MF with a normal immunophenotype but the prognosis has to he guarded in view of the rarity of this subtype.
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收藏
页码:158 / 163
页数:6
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