手术前利妥昔单抗治疗单中心Castleman病:临床病理结果

IF 2.4 3区 医学 Q2 HEMATOLOGY
Marco Paulli, Giuseppe Neri, Francesca Antoci, Edoardo D'Este, Marco Minetto, Federico Carpi, Martina La Fauci, Marcello Gambacorta, Marco Lucioni, Luca Arcaini
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引用次数: 0

摘要

Castleman病(CD)是一种罕见的淋巴细胞增生性疾病,具有独特的临床病理特征,包括单中心型(UCD)和多中心型(MCD)两种不同的临床亚型。UCD通常累及单个淋巴结,无或极少局部症状。组织学上,大多数UCD病例表现为退行性透明的血管生发中心,以穿透性血管、树突状增生/发育不良、滤泡间血管增多为特征。虽然完全手术切除是UCD的标准治疗方法,但也有用新辅助抗cd20治疗的病例报道。在这里,我们描述了一个用抗cd20治疗的UCD病例,它只显示出部分反应。我们详细介绍了治疗后手术标本的临床表现和组织学变化,并讨论了局部微环境对抗cd20治疗效果的潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unicentric Castleman disease treated with rituximab before surgery: clinicopathologic findings.

Castleman disease (CD) is a rare lymphoproliferative disorder with unique clinicopathological features, including two distinct clinical subtypes categorized as unicentric (UCD) and multicentric (MCD). UCD usually involves a single lymph node site presenting with no or minimal local symptoms. Histologically, most UCD cases exhibit regressive hyaline vascular germinal centers, characterized by penetrating vessels, dendritic hyperplasia/dysplasia, and increased interfollicular vascularity. While complete surgical excision is the standard treatment for UCD, cases treated with neoadjuvant anti-CD20 therapy have been reported. Here, we describe a UCD case treated with anti-CD20, that showed only a partial response. We detail the clinical findings and the histological changes observed in the surgical specimen following therapy, and discuss the potential influence of the local microenvironment on the therapeutic efficacy of anti-CD20.

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来源期刊
Annals of Hematology
Annals of Hematology 医学-血液学
CiteScore
5.60
自引率
2.90%
发文量
304
审稿时长
2 months
期刊介绍: Annals of Hematology covers the whole spectrum of clinical and experimental hematology, hemostaseology, blood transfusion, and related aspects of medical oncology, including diagnosis and treatment of leukemias, lymphatic neoplasias and solid tumors, and transplantation of hematopoietic stem cells. Coverage includes general aspects of oncology, molecular biology and immunology as pertinent to problems of human blood disease. The journal is associated with the German Society for Hematology and Medical Oncology, and the Austrian Society for Hematology and Oncology.
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