Hu H, Jiang Y J, Xu L, Yin L J, Liu X F, Yin S Y, Xu J J, He M X
Department of Pathology, Changhai Hospital, Naval Military Medical University, Shanghai 200433, China.
Zhonghua Bing Li Xue Za Zhi. 2023 Jul 8;52(7):702-709. doi: 10.3760/cma.j.cn112151-20230114-00040.
To investigate the value of plasma cells for diagnosing lymph node diseases. Common lymphadenopathy (except plasma cell neoplasms) diagnosed from September 2012 to August 2022 were selected from the pathological records of Changhai Hospital, Shanghai, China. Morphological and immunohistochemical features were analyzed to examine the infiltration pattern, clonality, and IgG and IgG4 expression of plasma cells in these lymphadenopathies, and to summarize the differential diagnoses of plasma cell infiltration in common lymphadenopathies. A total of 236 cases of lymphadenopathies with various degrees of plasma cell infiltration were included in the study. There were 58 cases of Castleman's disease, 55 cases of IgG4-related lymphadenopathy, 14 cases of syphilitic lymphadenitis, 2 cases of rheumatoid lymphadenitis, 18 cases of Rosai-Dorfman disease, 23 cases of Kimura's disease, 13 cases of dermal lymphadenitis and 53 cases of angioimmunoblastic T-cell lymphoma (AITL). The main features of these lymphadenopathies were lymph node enlargement with various degrees of plasm cell infiltration. A panel of immunohistochemical antibodies were used to examine the distribution of plasma cells and the expression of IgG and IgG4. The presence of lymph node architecture could help determine benign and malignant lesions. The preliminary classification of these lymphadenopathies was based on the infiltration features of plasma cells. The evaluation of IgG and IgG4 as a routine means could exclude the lymph nodes involvement of IgG4-related dieases (IgG4-RD), and whether it was accompanied by autoimmune diseases or multiple-organ diseases, which were of critical evidence for the differential diagnosis. For common lesions of lymphadenopathies, such as Castleman's disease, Kimura's disease, Rosai-Dorfman's disease and dermal lymphadenitis, the expression ratio of IgG4/IgG (>40%) as detected using immunhistochemistry and serum IgG4 levels should be considered as a standard for the possibility of IgG4-RD. The differential diagnosis of multicentric Castleman's diseases and IgG4-RD should be also considered. Infiltration of plasma cells and IgG4-positive plasma cells may be detected in some types of lymphadenopathies and lymphomas in clinicopathological daily practice, but not all of them are related to IgG4-RD. It should be emphasized that the characteristics of plasma cell infiltration and the ratio of IgG4/IgG (>40%) should be considered for further differential diagnosis and avoiding misclassification of lymphadenopathies.
探讨浆细胞在诊断淋巴结疾病中的价值。从中国上海长海医院2012年9月至2022年8月的病理记录中选取诊断为常见淋巴结病(浆细胞肿瘤除外)的病例。分析形态学和免疫组化特征,以研究这些淋巴结病中浆细胞的浸润模式、克隆性以及IgG和IgG4表达情况,并总结常见淋巴结病中浆细胞浸润的鉴别诊断。本研究共纳入236例有不同程度浆细胞浸润的淋巴结病病例。其中包括58例Castleman病、55例IgG4相关淋巴结病、14例梅毒性淋巴结炎、2例类风湿性淋巴结炎、18例Rosai-Dorfman病、23例木村病、13例皮肤淋巴结炎和53例血管免疫母细胞性T细胞淋巴瘤(AITL)。这些淋巴结病的主要特征是淋巴结肿大并伴有不同程度的浆细胞浸润。使用一组免疫组化抗体检测浆细胞的分布以及IgG和IgG4的表达。淋巴结结构的存在有助于判断病变的良恶性。这些淋巴结病的初步分类基于浆细胞的浸润特征。将IgG和IgG4检测作为常规手段可排除IgG4相关疾病(IgG4-RD)的淋巴结受累情况,以及其是否伴有自身免疫性疾病或多器官疾病,这是鉴别诊断的关键依据。对于淋巴结病的常见病变,如Castleman病、木村病、Rosai-Dorfman病和皮肤淋巴结炎,免疫组化检测的IgG4/IgG表达率(>40%)以及血清IgG4水平应作为判断IgG4-RD可能性的标准。还应考虑多中心Castleman病和IgG4-RD的鉴别诊断。在临床病理日常实践中,某些类型的淋巴结病和淋巴瘤可能检测到浆细胞浸润和IgG4阳性浆细胞,但并非所有这些都与IgG4-RD相关。应强调的是,为进一步进行鉴别诊断并避免淋巴结病的错误分类,应考虑浆细胞浸润特征以及IgG4/IgG比例(>40%)。