Post Ginell R, Bell Robert C, Rjoop Anwar, Lobo Rodolfo Henrich, Yuan Youzhong, Post Steven R
Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Ann Clin Lab Sci. 2016 Sep;46(5):474-9.
The objective of the study was to evaluate the expression pattern of interleukin-6 (IL-6) to determine its utility in differentiating Castleman Disease subtypes and reactive lymphadenopathies. Paraffin-embedded tissue blocks from 20 cases referred for assessment of Castleman Disease (CD) and 4 cases of reactive hyperplasia were selected for immunohistochemical staining with an IL-6 antibody. Six pathologists evaluated the hematoxylin and eosin stained tissue sections and IL-6 expression pattern. Of 20 CD referral cases, the pathologic diagnosis was CD in 14 cases and included 6 hyaline-vascular (HV-CD), 6 plasma cell (PC-CD) and 2 "mixed type"-CD cases. The remaining 6 referral cases showed morphologic features consistent with reactive lymphadenopathy. Patients with non-CD, reactive lymphadenopathies had clinical and/or laboratory features of systemic lupus erythematosus, Hashimoto's disease, viral infection or chronic cellulitis. The pattern of IL-6 expression differed between CD subtypes and non-CD cases. In PC-CD, IL-6 expression was detected in plasma cells and vascular endothelial cells; whereas IL-6 immunoreactivity was detected primarily in vascular endothelial cells in HV-CD. Interfollicular plasma cells were prominent in PC-CD and reactive lymphadenopathies; however, IL-6 expression was significantly increased in PC-CD compared to reactive lymph nodes. Together with morphologic features, the expression pattern of IL-6 detected by immunohistochemistry is helpful to distinguish CD subtypes and reactive mimics.
本研究的目的是评估白细胞介素-6(IL-6)的表达模式,以确定其在鉴别Castleman病亚型和反应性淋巴结病中的作用。选取20例因Castleman病(CD)评估而转诊的病例以及4例反应性增生病例的石蜡包埋组织块,用IL-6抗体进行免疫组织化学染色。6名病理学家评估苏木精和伊红染色的组织切片以及IL-6表达模式。在20例CD转诊病例中,14例病理诊断为CD,包括6例透明血管型(HV-CD)、6例浆细胞型(PC-CD)和2例“混合型”-CD病例。其余6例转诊病例表现出与反应性淋巴结病一致的形态学特征。非CD反应性淋巴结病患者具有系统性红斑狼疮、桥本氏病、病毒感染或慢性蜂窝织炎的临床和/或实验室特征。CD亚型和非CD病例之间的IL-6表达模式不同。在PC-CD中,IL-6在浆细胞和血管内皮细胞中表达;而在HV-CD中,IL-6免疫反应主要在血管内皮细胞中检测到。滤泡间浆细胞在PC-CD和反应性淋巴结病中较为突出;然而,与反应性淋巴结相比,PC-CD中的IL-6表达显著增加。结合形态学特征,免疫组织化学检测到的IL-6表达模式有助于区分CD亚型和反应性模仿病变。