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皮肤中CD30+ T细胞淋巴增殖性疾病的谱系

The spectrum of CD30+ T cell lymphoproliferative disorders in the skin.

作者信息

Kartan Saritha, Johnson William T, Sokol Kelsey, Alpdogan Onder, Gru Alejandro A, Nikbakht Neda, Porcu Pierluigi

机构信息

Division of Hematologic Malignancies and Hematopoietic Stem Cell Transplantation, Department of Medical Oncology, Thomas Jefferson University, Philadelphia, PA, USA.

Department of Pathology, University of Virginia, Charlottesville, VA, USA.

出版信息

Chin Clin Oncol. 2019 Feb;8(1):3. doi: 10.21037/cco.2018.12.03. Epub 2019 Jan 9.

Abstract

Primary cutaneous CD30+ T cell lymphoproliferative disorders (pcCD30+ T cell LPDs) are a spectrum of pre-malignant to frankly neoplastic lymphoproliferations that comprise lymphomatoid papulosis (LyP), primary cutaneous anaplastic large cell lymphoma (pcALCL), and borderline lesions. Although the atypical T cells that are the hallmark of these disorders share the expression of CD30, as the identifying marker, the clinical presentation, histological features and clinical course are vastly different. Furthermore, histopathologic features of pcCD30+ T cell LPDs may overlap with other cutaneous and systemic lymphomas. While most pcCD30+ T cell LPDs have an excellent prognosis, systemic lymphomas typically have a poorer outcome. CD30 has now been shown to be a reliable therapeutic target in pcCD30+ T cell LPDs. This review will emphasize the structure and function of CD30, along with the clinical and pathological spectrum of pcCD30+ T cell LPDs. It will also highlight other CD30+ lymphoproliferations that must be differentiated by careful clinical and pathological correlation.

摘要

原发性皮肤CD30 + T细胞淋巴增殖性疾病(pcCD30 + T细胞LPDs)是一系列从癌前病变到明显肿瘤性的淋巴增殖性疾病,包括淋巴瘤样丘疹病(LyP)、原发性皮肤间变性大细胞淋巴瘤(pcALCL)和交界性病变。尽管作为这些疾病标志的非典型T细胞都表达CD30这一识别标志物,但它们的临床表现、组织学特征和临床病程却大不相同。此外,pcCD30 + T细胞LPDs的组织病理学特征可能与其他皮肤和系统性淋巴瘤重叠。虽然大多数pcCD30 + T细胞LPDs预后良好,但系统性淋巴瘤通常预后较差。现已证明CD30是pcCD30 + T细胞LPDs中一个可靠的治疗靶点。本综述将重点介绍CD30的结构和功能,以及pcCD30 + T细胞LPDs的临床和病理谱。它还将强调其他必须通过仔细的临床和病理相关性进行鉴别的CD30 + 淋巴增殖性疾病。

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