IgG4相关疾病
病理
淋巴瘤
病变
医学
马尔特淋巴瘤
恶性肿瘤
免疫球蛋白轻链
活检
免疫球蛋白重链
假性淋巴瘤
淋巴增生
抗体
淋巴系统
疾病
免疫学
作者
Yasuharu Sato,Koh-ichi Ohshima,Katsuyoshi Takata,Xingang Huang,Wei Cui,Kyotaro Ohno,Tadashi Yoshino
出处
期刊:Journal of Clinical and Experimental Hematopathology
[Japanese Society for Lymphoreticular Tissue Research]
日期:2012-01-01
卷期号:52 (1): 51-55
被引量:49
摘要
IgG4-related disease is a recently proposed clinical entity with several unique clinicopathological features. A chronic inflammatory state with marked fibrosis, which can often be mistaken for malignancy, especially by clinical imaging analyses, unifies these features. In the present report, we describe a case of IgG4-producing mucosa-associated lymphoid tissue lymphoma mimicking IgG4-related disease. The patient was a 55-year-old male who was being followed for right orbital tumor over 1.5 years. The lesion had recently increased in size, so a biopsy was performed. Histologically, the lesion was consistent with IgG4-related disease ; however, IgG4+ plasma cells showed immunoglobulin light-chain restriction and immunoglobulin heavy chain gene rearrangement was detected in the lesion. Therefore, the lesion was diagnosed as IgG4-producing mucosa-associated lymphoid tissue lymphoma. In conclusion, in histological diagnosis of IgG4-related disease, it is important to examine not only IgG4-immunostain but also immunoglobulin light-chain restriction.
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