MR Imaging of IgG4-Related Disease in the Head and Neck and Brain

被引:87
作者
Toyoda, K. [1 ]
Oba, H. [1 ]
Kutomi, K. [1 ]
Furui, S. [1 ]
Oohara, A. [2 ]
Mori, H. [3 ]
Sakurai, K. [4 ]
Tsuchiya, K. [2 ]
Kan, S. [5 ]
Numaguchi, Y. [6 ]
机构
[1] Teikyo Univ, Sch Med, Dept Radiol, Tokyo 173, Japan
[2] Kyorin Univ, Sch Med, Dept Radiol, Tokyo, Japan
[3] Univ Tokyo, Dept Radiol, Grad Sch, Tokyo, Japan
[4] Nagoya City Univ, Grad Sch Med Sci, Dept Radiol, Nagoya, Aichi, Japan
[5] Kitasato Univ, Sch Med, Dept Diagnost Radiol, Kanagawa, Japan
[6] St Lukes Int Hosp, Dept Radiol, Tokyo, Japan
关键词
AUTOIMMUNE PANCREATITIS; DIAGNOSTIC-CRITERIA; MIKULICZS-DISEASE;
D O I
10.3174/ajnr.A3147
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
IgG4-related disease is characterized by histologic fibrosis with IgG4-positive plasma cell infiltration. Our study evaluated MR imaging features of IgG4-related disease in the head and neck and brain. Images from 15 patients were retrospectively evaluated for the location, signal intensity, and enhancement patterns of lesions. Lacrimal gland enlargement was observed in 8 cases. Other lesions included orbital pseudotumor in 5, pituitary enlargement in 5, and cranial nerve enlargement in 7; the infraorbital nerve was involved in 4. All lesions were hypointense on T2-weighted images, which is typical for IgG4-related lesions. Multiple sites were involved in the head and neck and brain in 11 patients. The diagnosis of IgG4-related disease should be considered in a patient presenting with T2 hypointense lacrimal gland, pituitary, or cranial nerve enlargement, or a T2 hypointense orbital mass, especially if multiple sites in the head and neck are involved in the presence of elevated serum IgG4.
引用
收藏
页码:2136 / 2139
页数:4
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