Gurwale Sushama Govindrao, Gore Charusheela Rajesh, Gulati Ishita, Dey Indranil
Department of Pathology, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth, Pimpri, Pune, Maharashtra, India.
J Oral Maxillofac Pathol. 2020 Feb;24(Suppl 1):S135-S138. doi: 10.4103/jomfp.JOMFP_83_17. Epub 2020 Feb 28.
Chronic sclerosing sialadenitis is associated with the immunoglobulin G4 (IgG4)-related disease (RD) spectrum. IgG4-RD is a newly recognized immunomediated fibroinflammatory condition characterized by several features: a tendency to form tumefactive lesions at multiple sites, lymphoplasmacytic infiltrate, fibrosis and obliterative phlebitis. Often but not always, the serum IgG4 concentrations are also elevated. Immunohistochemistry for IgG4 is helpful to clinch the diagnosis. Here, we describe a case of 65-year-old male with IgG4-related chronic sclerosing sialadenitis of the s ubmandibular gland. We have discussed the histopathological criteria to diagnose this entity.
慢性硬化性涎腺炎与免疫球蛋白G4(IgG4)相关疾病(RD)谱有关。IgG4相关疾病是一种新认识的免疫介导的纤维炎性疾病,具有以下几个特征:倾向于在多个部位形成肿块性病变、淋巴浆细胞浸润、纤维化和闭塞性静脉炎。血清IgG4浓度通常(但并非总是)也会升高。IgG4免疫组化有助于确诊。在此,我们描述一例65岁男性患有下颌下腺IgG4相关慢性硬化性涎腺炎的病例。我们讨论了诊断该疾病的组织病理学标准。