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蕈样肉芽肿和塞扎里综合征。

Mycosis Fungoides and Sezary Syndrome.

作者信息

Foss Francine M, Girardi Michael

机构信息

Hematology and Bone Marrow Transplantation, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06510, USA.

Department of Dermatology, Yale University School of Medicine, New Haven, CT 06510, USA.

出版信息

Hematol Oncol Clin North Am. 2017 Apr;31(2):297-315. doi: 10.1016/j.hoc.2016.11.008.

Abstract

Mycosis fungoides and the Sezary syndrome (SS) are rare lymphomas of CD4 helper T cells. There is stagewise progression from patch/plaques to thicker tumor lesions/diffuse erythroderma. Blood involvement is a characteristic of SS. Outcomes are related to the extent of skin, blood, lymph node, and visceral organ involvement. Patients with limited patch and plaque disease are treated with skin-directed therapies. More advanced/refractory disease is treated with skin-directed therapies and oral or systemic immunomodulatory agents. Single-agent chemotherapies are used against tumors, refractory plaques, and lymph node and visceral involvement. Allogeneic stem cell transplantation is a potentially curative strategy for advanced/resistant disease.

摘要

蕈样肉芽肿和塞扎里综合征(SS)是罕见的CD4辅助性T细胞淋巴瘤。其病程呈阶段性进展,从斑片/斑块发展为更厚的肿瘤性病变/弥漫性红皮病。血液受累是SS的一个特征。预后与皮肤、血液、淋巴结和内脏器官的受累程度相关。局限性斑片和斑块状疾病患者采用针对皮肤的治疗方法。更晚期/难治性疾病则采用针对皮肤的治疗方法以及口服或全身性免疫调节药物进行治疗。单药化疗用于治疗肿瘤、难治性斑块以及淋巴结和内脏受累情况。异基因干细胞移植是晚期/耐药性疾病的一种潜在治愈策略。

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