有色皮肤患者皮肤t细胞淋巴瘤的免疫发病机制。第二部分:ssamzary综合征

Nina C. Nwade , Sachi I. Desse , Akanksha Nagarkar , Nia E.R. James , Ryan Svoboda , Ginette A. Okoye , Jillian M. Richmond , Angel S. Byrd
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摘要

皮肤T细胞淋巴瘤(CTCL)是许多存在于皮肤中或在皮肤中循环的淋巴瘤的总称。其中一种系统性淋巴瘤是Sézary综合征(SS)。尽管SS在有色人种皮肤(SOC)中并不常见,但少数患者的表现确实与白人患者不同。在这篇图表综述中,我们提供了SS免疫发病机制和不同表现的概述。此外,还提供了当前治疗方案的摘要,重点介绍了正在进行的临床试验以及纳入SOC患者以促进健康公平的机会。SOC患者往往由于生物学差异和健康差异导致诊断延迟而预后较差。这体现了精准医疗实施的潜在优势和有前景的解决方案。为此,总结了精准医疗的影响和效益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunopathogenesis of cutaneous T-cell lymphoma in skin of color patients part 2: Sézary syndrome

Cutaneous T-cell lymphoma (CTCL) serves as an umbrella term for numerous lymphomas that reside in or recirculate through the skin. One such systemic lymphoma is Sézary Syndrome (SS). Although SS is not as common in Skin of Color (SOC), minority patients presenting with the condition do have a different presentation than their White counterparts. In this graphical review, we provide an overview of SS immunopathogenesis and varying presentations. Additionally, a summary of current treatment options is provided, highlighting ongoing clinical trials and opportunities to include SOC patients to promote health equity. SOC patients often have poorer prognosis due to biological differences and health disparities resulting in delayed diagnosis. This exemplifies the potential advantages and promising solutions of precision medicine implementation. To this end, the impact and benefits of precision medicine are summarized.

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