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[单中心Castleman病。症状、诊断与治疗]

[Unicentric Castlemans disease. Symptoms, diagnostics and therapy].

作者信息

Adam Zdeněk, Řehák Zdeněk, Adamová Zuzana, Koukalová Renata, Pour Luděk, Krejčí Marta, Boichuk Ivanna, Krejčí Martin, Štork Martin, Ševčíková Sabina, Král Zdeněk

出版信息

Vnitr Lek. 2021 Winter;67(8):465-473.

PMID:35459366
Abstract

Castleman disease (CD) includes a group of rare and heterogeneous disorders with characteristic lymph node histopathological abnormalities. CD can occur in a single lymph node station, which is referred to as unicentric CD (UCD). CD can also involve multicentric lymphadenopathy and inflammatory symptoms - multicentric Castleman disease. The first-ever diagnostic and treatment guidelines were recently developed for UCD and published 2020. Complete surgical resection is often curative and is therefore the preferred first-line therapy, if possible. The management of unresectable UCD is more challenging. Existing evidence supports that asymptomatic unresectable UCD may be observed. The anti-interleukin-6 monoclonal antibody siltuximab should be considered for unresectable UCD patients with an inflammatory syndrome. Unresectable UCD that is symptomatic because of compression of vital neighbouring structures may be rendered amenable to resection by medical therapy (rituximab, steroids), radiotherapy, or embolization. In this article, we report about the symptoms of this disease and about the diagnostics recommendation published in the International, evidence-based consensus diagnostic criteria for HHV-8-negative/ idiopathic multicentric Castleman disease and about the therapeutic recommendation published in International evidence-based consensus diagnostic and treatment guidelines for unicentric Castleman disease published in the year 2020.

摘要

Castleman病(CD)包括一组罕见且异质性的疾病,具有特征性的淋巴结组织病理学异常。CD可发生于单个淋巴结部位,称为单中心Castleman病(UCD)。CD也可累及多中心淋巴结病及炎症症状,即多中心Castleman病。最近首次制定了UCD的诊断和治疗指南,并于2020年发布。完整的手术切除通常可治愈,因此如果可能,是首选的一线治疗方法。不可切除的UCD的管理更具挑战性。现有证据支持,对于无症状的不可切除UCD可进行观察。对于有炎症综合征的不可切除UCD患者,应考虑使用抗白细胞介素-6单克隆抗体司妥昔单抗。因邻近重要结构受压而出现症状的不可切除UCD,可通过药物治疗(利妥昔单抗、类固醇)、放疗或栓塞使其适合切除。在本文中,我们报告了这种疾病的症状、国际上基于循证的HHV-8阴性/特发性多中心Castleman病共识诊断标准中发布的诊断建议,以及2020年发布的国际基于循证的单中心Castleman病共识诊断和治疗指南中发布的治疗建议。

相似文献

1
[Unicentric Castlemans disease. Symptoms, diagnostics and therapy].[单中心Castleman病。症状、诊断与治疗]
Vnitr Lek. 2021 Winter;67(8):465-473.
2
International evidence-based consensus diagnostic and treatment guidelines for unicentric Castleman disease.国际循证共识性单中心Castleman 病诊断与治疗指南。
Blood Adv. 2020 Dec 8;4(23):6039-6050. doi: 10.1182/bloodadvances.2020003334.
3
[Multicentric Castlemans disease. Symptoms, diagnostics and therapy].[多中心性Castleman病。症状、诊断与治疗]
Vnitr Lek. 2022 Winter;68(1):41-53.
4
International, evidence-based consensus treatment guidelines for idiopathic multicentric Castleman disease.特发性多中心 Castleman 病的国际、循证共识治疗指南。
Blood. 2018 Nov 15;132(20):2115-2124. doi: 10.1182/blood-2018-07-862334. Epub 2018 Sep 4.
5
Clinical and pathological characteristics of HIV- and HHV-8-negative Castleman disease.HIV和HHV-8阴性的Castleman病的临床和病理特征
Blood. 2017 Mar 23;129(12):1658-1668. doi: 10.1182/blood-2016-11-748855. Epub 2017 Jan 18.
6
Recent Advances in Castleman Disease.卡斯特曼病的最新进展。
Oncol Res Treat. 2022;45(11):693-704. doi: 10.1159/000526640. Epub 2022 Oct 11.
7
[Not Available].[无可用内容]
Rev Med Interne. 2022 Dec;43(10S1):10S4-10S9. doi: 10.1016/S0248-8663(23)00019-X.
8
Castleman Disease: A Multicenter Case Series from Turkey.血管滤泡性淋巴结增生症:来自土耳其的多中心病例系列。
Turk J Haematol. 2022 Jun 1;39(2):130-135. doi: 10.4274/tjh.galenos.2022.2021.0670. Epub 2022 Feb 18.
9
The French paediatric cohort of Castleman disease: a retrospective report of 23 patients.法国小儿血管滤泡性淋巴结增生症队列研究:23 例患儿的回顾性报告。
Orphanet J Rare Dis. 2020 Apr 17;15(1):95. doi: 10.1186/s13023-020-1345-5.
10
Virome capture sequencing does not identify active viral infection in unicentric and idiopathic multicentric Castleman disease.病毒组捕获测序不能在局灶性和特发性多中心 Castleman 病中识别出活跃的病毒感染。
PLoS One. 2019 Jun 26;14(6):e0218660. doi: 10.1371/journal.pone.0218660. eCollection 2019.

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