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本文引用的文献

1
Castleman disease in pediatrics: Insights on presentation, treatment, and outcomes from a two-site retrospective cohort study.儿科Castleman 病:来自两院区回顾性队列研究的临床表现、治疗和结局相关见解。
Pediatr Blood Cancer. 2019 May;66(5):e27613. doi: 10.1002/pbc.27613. Epub 2019 Jan 24.
2
Recurrent PDGFRB mutations in unicentric Castleman disease.单中心Castleman病中的复发性血小板衍生生长因子受体B(PDGFRB)突变
Leukemia. 2019 Apr;33(4):1035-1038. doi: 10.1038/s41375-018-0323-6. Epub 2019 Jan 3.
3
Masked pemphigus among pediatric patients with Castleman's disease.Castleman病患儿中的隐匿性天疱疮。
Int J Rheum Dis. 2019 Jan;22(1):121-131. doi: 10.1111/1756-185X.13407. Epub 2018 Nov 8.
4
A novel mutation with variable expressivity in a family with unicentric and idiopathic multicentric Castleman disease.一个家族中存在单一中心型和特发性多中心型血管滤泡性淋巴结增生症的具有可变外显率的新型突变。
Blood Adv. 2018 Nov 13;2(21):2959-2963. doi: 10.1182/bloodadvances.2018023911.
5
The clinicopathological comparison among nodal cases of idiopathic multicentric Castleman disease with and without TAFRO syndrome.特发性多中心 Castleman 病伴与不伴 TAFRO 综合征的淋巴结病例的临床病理比较。
Hum Pathol. 2018 Jul;77:130-138. doi: 10.1016/j.humpath.2018.04.001. Epub 2018 Apr 21.
6
Renal failure in pediatric Castleman disease: Four French cases with thrombotic microangiopathy.小儿血管滤泡性淋巴结增生症致肾衰竭:4 例合并血栓性微血管病病例报告
Pediatr Blood Cancer. 2018 Jul;65(7):e27045. doi: 10.1002/pbc.27045. Epub 2018 Mar 30.
7
Next-generation sequencing of idiopathic multicentric and unicentric Castleman disease and follicular dendritic cell sarcomas.特发性多中心和单中心 Castleman 病及滤泡树突状细胞肉瘤的下一代测序。
Blood Adv. 2018 Mar 13;2(5):481-491. doi: 10.1182/bloodadvances.2017009654.
8
Clinical, laboratory and imaging findings in Castleman's disease - The subtype decides.Castleman 病的临床、实验室和影像学表现——亚型决定。
Blood Rev. 2018 May;32(3):225-234. doi: 10.1016/j.blre.2017.11.005. Epub 2017 Nov 29.
9
Unicentric Castleman Disease.单中心Castleman病
Hematol Oncol Clin North Am. 2018 Feb;32(1):65-73. doi: 10.1016/j.hoc.2017.09.006.
10
Diagnosis of Castleman Disease.Castleman病的诊断
Hematol Oncol Clin North Am. 2018 Feb;32(1):53-64. doi: 10.1016/j.hoc.2017.09.005.

儿童症状性和无症状性 Castleman 病的组织学和实验室特征。

Histologic and Laboratory Characteristics of Symptomatic and Asymptomatic Castleman Disease in the Pediatric Population.

机构信息

Department of Laboratories, Seattle Children's Hospital, Seattle, WA.

Department of Laboratory Medicine, University of Washington, Seattle.

出版信息

Am J Clin Pathol. 2020 May 5;153(6):821-832. doi: 10.1093/ajcp/aqaa011.

DOI:10.1093/ajcp/aqaa011
PMID:32112075
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7453143/
Abstract

OBJECTIVES

Compare the morphologic, laboratory, and clinical features of asymptomatic and symptomatic Castleman disease in the pediatric population.

METHODS

We reviewed clinical records and histopathology of patients with Castleman disease from 2 pediatric institutions.

RESULTS

Of 39 patients with pediatric Castleman disease, 37 had unicentric disease, all classified with the hyaline vascular variant of Castleman disease, 8 of which were clinically symptomatic. These 8 patients demonstrated abnormal laboratory findings, including microcytic anemia, elevated erythrocyte sedimentation rate and C-reactive protein, and hypoalbuminemia. In addition, histopathologic evaluation showed that the 8 symptomatic cases had more hyperplastic germinal centers, fewer atrophic or regressed germinal centers, fewer mantle zones containing multiple germinal centers, reduced "onion skinning" of mantle zones, and fewer "lollipop" formations compared with the asymptomatic cases.

CONCLUSIONS

This series of pediatric Castleman disease showed that lymph nodes from asymptomatic patients generally demonstrated the more classic hyaline vascular histology, whereas those with symptoms could lack or have only focal classic findings. As such, reactive lymph nodes with subtle Castleman-like features should prompt clinical correlation to ensure proper diagnosis.

摘要

目的

比较儿童人群中无症状和有症状的巨大淋巴结增生症的形态学、实验室和临床特征。

方法

我们回顾了 2 家儿科机构中患有巨大淋巴结增生症的患者的临床记录和组织病理学。

结果

39 例患有小儿巨大淋巴结增生症的患者中,37 例为单中心疾病,均归类为透明血管型巨大淋巴结增生症,其中 8 例为临床症状性。这 8 例患者表现出异常的实验室发现,包括小细胞性贫血、红细胞沉降率和 C 反应蛋白升高以及低白蛋白血症。此外,组织病理学评估显示,与无症状病例相比,8 例有症状病例具有更多的增生性生发中心、更少的萎缩或退化的生发中心、更少包含多个生发中心的套区、套区的“洋葱皮”减少以及更少的“棒棒糖”形成。

结论

本系列儿童巨大淋巴结增生症表明,无症状患者的淋巴结通常表现出更典型的透明血管组织病理学特征,而有症状的患者可能缺乏或仅有局灶性典型表现。因此,具有微妙巨大淋巴结增生样特征的反应性淋巴结应引起临床相关性以确保正确诊断。