Holloway K B, Flowers F P, Ramos-Caro F A
Department of Medicine, University of Florida College of Medicine, Gainesville.
J Am Acad Dermatol. 1992 Sep;27(3):367-78. doi: 10.1016/0190-9622(92)70202-q.
Mycosis fungoides and Sézary syndrome, collectively referred to as cutaneous T-cell lymphoma, are non-Hodgkin's lymphomas that initially appear in the skin. Early-stage disease, limited to the skin, is best treated with sequential topical therapies such as topical nitrogen mustard, psoralen phototherapy (PUVA), or total-skin electron beam therapy. Photopheresis is the first line of therapy for the patient with erythroderma. Systemic therapy is generally reserved for patients with refractory disease and patients who initially present with extracutaneous involvement. Although there are several treatment options for cutaneous T-cell lymphoma, there have been few randomized comparative trials.
蕈样肉芽肿和 Sézary 综合征统称为皮肤 T 细胞淋巴瘤,是非霍奇金淋巴瘤,最初出现在皮肤中。局限于皮肤的早期疾病,最好采用序贯局部治疗,如局部使用氮芥、补骨脂素光化学疗法(PUVA)或全身皮肤电子束疗法。光分离置换疗法是红皮病患者的一线治疗方法。全身治疗通常适用于难治性疾病患者和最初表现为皮肤外受累的患者。虽然皮肤 T 细胞淋巴瘤有几种治疗选择,但很少有随机对照试验。