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生殖细胞肿瘤相关性淋巴组织增生性疾病:系统综述。

Germinotropic lymphoproliferative disorder: a systematic review.

机构信息

Pathology Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Surgical Oncology Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

出版信息

Ann Hematol. 2020 Oct;99(10):2243-2253. doi: 10.1007/s00277-020-04024-3. Epub 2020 Apr 19.

Abstract

Germinotropic lymphoproliferative disorder is a rare and rather enigmatic novel entity with distinctive clinicopathological features, one of which is the typical co-infection by Human herpesvirus 8 and Epstein-Barr virus. Human herpesvirus 8 is a lymphotropic virus detected in Kaposi sarcoma, multicentric Castleman disease, primary effusion lymphoma, Human herpesvirus 8-positive diffuse large B cell lymphoma not otherwise specified, and germinotropic lymphoproliferative disorder. Co-infection by Human herpesvirus 8 and Epstein-Barr virus is identified only in two lymphoproliferative diseases: germinotropic lymphoproliferative disorder and primary effusion lymphoma, which are otherwise diseases with totally different clinical presentations and outcomes. Unlike primary effusion lymphoma mostly occurring in immunocompromised individuals and following an aggressive course, germinotropic lymphoproliferative disorder usually presents with single or multiple lymphadenopathy affecting mainly immunocompetent individuals and mostly follows an indolent course. Based on the PRISMA guidelines, we carried out a systematic search on PubMed/MEDLINE, Web of Science, Scopus, EMBASE, and Cochrane Library using the search terms "germinotropic" and "lymphoproliferative disorder." Current scientific literature reports just 19 cases of germinotropic lymphoproliferative disorder. The purpose of our systematic review is to improve our understanding of the disease, focusing on epidemiology, clinical presentation, pathological features, treatment, and outcome. In addition, we discuss the differential diagnosis with the other Human herpesvirus 8-related lymphoproliferative diseases as currently recognized in the World Health Organization classification, adding a focus on lymphoproliferative disorders showing overlapping features.

摘要

生殖细胞亲淋巴组织增生性疾病是一种罕见且相当神秘的新型实体,具有独特的临床病理特征,其中之一是典型的人疱疹病毒 8 型和 Epstein-Barr 病毒共同感染。人疱疹病毒 8 型是一种在卡波西肉瘤、多中心 Castleman 病、原发性渗出性淋巴瘤、人疱疹病毒 8 阳性弥漫性大 B 细胞淋巴瘤未另作说明和生殖细胞亲淋巴组织增生性疾病中检测到的亲淋巴病毒。人疱疹病毒 8 型和 Epstein-Barr 病毒的共同感染仅在两种淋巴组织增生性疾病中被识别:生殖细胞亲淋巴组织增生性疾病和原发性渗出性淋巴瘤,这两种疾病在临床表现和结局上完全不同。与主要发生在免疫功能低下个体并呈侵袭性病程的原发性渗出性淋巴瘤不同,生殖细胞亲淋巴组织增生性疾病通常表现为单个或多个淋巴结病,主要影响免疫功能正常的个体,且大多呈惰性病程。根据 PRISMA 指南,我们使用“germinotropic”和“lymphoproliferative disorder”这两个检索词,在 PubMed/MEDLINE、Web of Science、Scopus、EMBASE 和 Cochrane Library 上进行了系统搜索。目前的科学文献仅报道了 19 例生殖细胞亲淋巴组织增生性疾病。本系统综述的目的是提高对该疾病的认识,重点关注流行病学、临床表现、病理特征、治疗和结局。此外,我们还讨论了与目前在世界卫生组织分类中被认可的其他与人疱疹病毒 8 相关的淋巴组织增生性疾病的鉴别诊断,并重点关注具有重叠特征的淋巴组织增生性疾病。

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