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原发性皮肤T细胞淋巴瘤:蕈样肉芽肿和塞扎里综合征。

Primary Cutaneous T-Cell Lymphomas: Mycosis Fungoides and Sezary Syndrome.

作者信息

Querfeld Christiane, Zain Jasmine, Rosen Steven T

机构信息

Division of Dermatology, City of Hope, 1500 E. Duarte Road, Duarte, CA, 91010, USA.

Department of Hematology/Hematopoietic Cell Transplantation, Duarte, USA.

出版信息

Cancer Treat Res. 2019;176:225-248. doi: 10.1007/978-3-319-99716-2_11.

Abstract

Mycosis fungoides and Sézary syndrome are the most common subtypes of all primary cutaneous lymphomas and represent complex diseases that require a multidisciplinary assessment by dermatologists, oncologists, and pathologists. Staging and work-up are critical to guarantee an optimal treatment plan that includes skin-directed and/or systemic regimens depending on the clinical stage, tumor burden, drug-related side effect profile, and patient comorbidities. However, there is no cure and patients frequently relapse, requiring repeated treatment courses for disease control. The study of the tumor microenvironment and molecular mechanisms of these rare neoplasms may assist in the development of new immune therapies providing promising treatment approaches tailored for patients with relapse/refractory disease.

摘要

蕈样肉芽肿和塞扎里综合征是所有原发性皮肤淋巴瘤中最常见的亚型,是复杂的疾病,需要皮肤科医生、肿瘤学家和病理学家进行多学科评估。分期和检查对于确保制定最佳治疗方案至关重要,该方案根据临床分期、肿瘤负荷、药物相关副作用情况和患者合并症,包括针对皮肤的和/或全身治疗方案。然而,无法治愈,患者常复发,需要反复进行治疗疗程以控制疾病。对这些罕见肿瘤的肿瘤微环境和分子机制的研究可能有助于开发新的免疫疗法,为复发/难治性疾病患者提供有前景的量身定制的治疗方法。

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