Nakashima Yoshikazu, Nakamura Hideki, Horai Yoshiro, Hayashi Tomayoshi, Takagi Yukinori, Nakamura Takashi, Kawakami Atsushi
Department of Immunology and Rheumatology, Unit of Translational Medicine, Nagasaki University Graduate School of Biomedical Sciences , Nagasaki , Japan.
Mod Rheumatol. 2015 May;25(3):462-7. doi: 10.3109/14397595.2013.843750. Epub 2014 Mar 4.
A 63-year-old man with enlargement of the bilateral submandibular glands visited with elevated serum IgG4. A biopsy specimen showed plasma cell infiltration with more than 50% IgG4/IgG staining, suggesting the existence of IgG4-related disease (IgG4-RD). Positive anti-SS-A/Ro antibody and the labial salivary gland's biopsy suggested existence of primary Sjögren's syndrome (pSS). Administration of glucocorticoid improved the serum IgG4 level while reducing the submandibular gland lesions. Positive TUNEL staining suggested the coexistence of IgG4-RD and pSS.
一名63岁男性因双侧颌下腺肿大就诊,血清IgG4升高。活检标本显示浆细胞浸润,IgG4/IgG染色超过50%,提示存在IgG4相关疾病(IgG4-RD)。抗SS-A/Ro抗体阳性及唇腺活检提示存在原发性干燥综合征(pSS)。给予糖皮质激素后,血清IgG4水平改善,颌下腺病变减轻。TUNEL染色阳性提示IgG4-RD和pSS共存。