Department of Laboratories, Seattle Children's Hospital, Seattle, WA.
Department of Laboratory Medicine, University of Washington, Seattle.
Am J Clin Pathol. 2020 May 5;153(6):821-832. doi: 10.1093/ajcp/aqaa011.
Compare the morphologic, laboratory, and clinical features of asymptomatic and symptomatic Castleman disease in the pediatric population.
We reviewed clinical records and histopathology of patients with Castleman disease from 2 pediatric institutions.
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.
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.
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。
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。
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。
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。