Spontaneous Regression of Swollen Submandibular Glands in IgG4-Related Disease

被引:0
作者
Suzuki, Masanobu [1 ,2 ,3 ]
Nakamaru, Yuji [1 ,2 ]
Takagi, Dai [1 ,2 ]
Honma, Aya [1 ,2 ]
Suzuki, Takayoshi [1 ,2 ,4 ]
Takakuwa, Emi [4 ]
Morita, Shinya [1 ,2 ]
Vreugde, Sarah [3 ]
Homma, Akihiro [1 ,2 ]
机构
[1] Hokkaido Univ, Fac Med, Dept Otolaryngol Head & Neck Surg, Sapporo, Hokkaido, Japan
[2] Hokkaido Univ, Grad Sch Med, Sapporo, Hokkaido, Japan
[3] Univ Adelaide, Queen Elizabeth Hosp, Dept Surg Otorhinolaryngol Head & Neck Surg, Adelaide, SA, Australia
[4] Hokkaido Univ, Hokkaido Univ Hosp, Grad Sch Med, Dept Surg Pathol, Sapporo, Hokkaido, Japan
关键词
IgG4-related disease; Mikulicz disease; spontaneous regression; complement; volume; predictor; submandibular glands; biomarker; autoimmune pancreatitis; salivary glands; COMPLEMENT; IGG4; ACTIVATION;
D O I
10.1177/2152656718816738
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background IgG4-related disease is a new clinical entity frequently associated with swelling of the submandibular glands (SMGs). The long-term outcome of SMG swelling without steroid therapy remains unknown. Objective To examine whether swollen SMGs spontaneously regress without steroid therapy in the context of IgG4-related disease and to identify biomarkers that can predict the spontaneous regression of SMG swelling. Methods The SMG volume of 49 patients diagnosed with IgG4-related disease was calculated by measuring the axial and coronal planes of computed tomography scans. The change in SMG volume over time was measured and examined by treatment regimen, clinical data, and serum complement level. Results We found 28 of 49 (57%) IgG4-related disease patients to have swollen SMGs, with 15 of 20 (75%) of the swollen SMGs regressing without steroid therapy. The time required for the SMGs swelling to regress was significantly shorter in the steroid therapy group than in the no-steroid therapy group. Serum complement components at the initial visit were significantly lower in the regressed SMG group than in the nonregressed SMG group. Conclusion We observed 75% of swollen SMGs spontaneously regressed in patients with IgG4-related disease. The time required for the swollen SMGs to regress was longer in patients without steroid therapy than in those with steroid therapy. Serum complement level could be used as a predictor for the spontaneous regression of swollen SMGs in patients with IgG4-related disease.
引用
收藏
页数:8
相关论文
共 50 条
[21]   The clinical spectrum of IgG4-related disease [J].
Brito-Zeron, Pilar ;
Ramos-Casals, Manuel ;
Bosch, Xavier ;
Stone, John H. .
AUTOIMMUNITY REVIEWS, 2014, 13 (12) :1203-1210
[22]   DNA Microarray Analysis of Submandibular Glands in IgG4-Related Disease Indicates a Role for MARCO and Other Innate Immune-Related Proteins [J].
Ohta, Miho ;
Moriyama, Masafumi ;
Maehara, Takashi ;
Gion, Yuka ;
Furukawa, Sachiko ;
Tanaka, Akihiko ;
Hayashida, Jun-Nosuke ;
Yamauchi, Masaki ;
Ishiguro, Noriko ;
Mikami, Yurie ;
Tsuboi, Hiroto ;
Iizuka-Koga, Mana ;
Kawano, Shintaro ;
Sato, Yasuharu ;
Kiyoshima, Tamotsu ;
Sumida, Takayuki ;
Nakamura, Seiji .
MEDICINE, 2016, 95 (07) :e2853
[23]   Submandibular gland tissue RNAseq and spatial transcriptome analyses in IgG4-related disease [J].
Yamamoto, Motohisa ;
Kamekura, Ryuta ;
Uehara, Masaaki ;
Ichii, Yuta ;
Tanaka, Tomonao ;
Aochi, Satsuki ;
Takano, Ken-ichi .
RHEUMATOLOGY, 2025, 64 (04) :2265-2271
[24]   Possible participation of IgG4 in the activation of complement in IgG4-related disease with hypocomplementemia [J].
Sugimoto, Mitsuru ;
Watanabe, Hiroshi ;
Asano, Tomoyuki ;
Sato, Shuzo ;
Takagi, Tadayuki ;
Kobayashi, Hiroko ;
Ohira, Hiromasa .
MODERN RHEUMATOLOGY, 2016, 26 (02) :251-258
[25]   CT features and pathologic characteristics of IgG4-related systemic disease of submandibular gland [J].
Wang, Zhiwei ;
Feng, Ruie ;
Chen, Yu ;
Duan, Miao ;
Wang, Man ;
Jin, Zhengyu ;
Rumboldt, Zoran ;
Zhang, Zhuhua .
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2015, 8 (12) :16111-16116
[26]   Management of IgG4-related disease [J].
Zhong, Wen ;
Stone, John H. .
LANCET RHEUMATOLOGY, 2019, 1 (01) :E55-E65
[27]   IgG4-related sclerosing disease [J].
Kamisawa, Terumi ;
Okamoto, Atsutake .
WORLD JOURNAL OF GASTROENTEROLOGY, 2008, 14 (25) :3948-3955
[28]   IgG4-Related Disease and Malignancy [J].
Yamamoto, Motohisa ;
Takahashi, Hiroki ;
Shinomura, Yasuhisa .
INTERNAL MEDICINE, 2012, 51 (04) :349-350
[29]   The Histopathology of IgG4-Related Disease [J].
Avincsal, Mehmet Ozgur ;
Zen, Yoh .
IGG4-RELATED DISEASE, 2017, 401 :45-60
[30]   Histopathology of IgG4-related disease [J].
Detlefsen, S. ;
Kloeppel, G. .
ZEITSCHRIFT FUR RHEUMATOLOGIE, 2016, 75 (07) :666-674