IgG4-Related Inflammatory Pseudotumor Involving the Clivus: A Case Report and Literature Review

被引:4
|
作者
Liu, Xiaohai [1 ,2 ]
Wang, Renzhi [2 ,3 ]
Li, Mingchu [1 ,2 ]
Chen, Ge [1 ,2 ]
机构
[1] Capital Med Univ, Dept Neurosurg, Xuanwu Hosp, Beijing, Peoples R China
[2] Chinese Pituitary Specialists Congress, Beijing, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Neurosurg, Beijing, Peoples R China
来源
关键词
IgG4-related disease; IgG4-related inflammatory pseudotumor; clivus; endoscopic transsphenoidal approach; case report;
D O I
10.3389/fendo.2021.666791
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IgG4-related inflammatory pseudotumors are very uncommon and are characterized histologically by the presence of inflammatory swellings with increasing IgG4-positive plasma cells and lymphocytes infiltrating the tissues. As reports of intracranial IgG4-related pseudotumors are very rare, we report a case of an IgG4-related inflammatory pseudotumor involving the clivus mimicking meningioma. A 46-year-old male presented with intermittent headache for 2 years and a sudden onset of dysphagia and dysphonia of 7 days' duration along with lower limb weakness. Enhanced magnetic resonance imaging (MRI) of the skull base revealed an isointense signal on T1- and T2-weighted images from an enhanced mass located at the middle of the upper clivus region, for which a meningioma was highly suspected. Then, an endoscopic transsphenoidal approach was adopted and the lesion was partially resected, as the subdural extra-axial lesion was found to be very tough and firm, exhibiting fibrous scarring attaching to the brain stem and basal artery. After the surgery, brain stem and posterior cranial nerve decompression was achieved, and the patient's symptoms, such as dysphagia, dysphonia and lower limb weakness, improved. Pathological findings showed many IgG4-positive plasma cells and lymphocytes surrounded by collagen-rich fibers. The patient was sent to the rheumatology department for further glucocorticoids after the diagnosis of an IgG4-related inflammatory pseudotumor was made. This case highlights the importance of considering IgG4-related inflammatory pseudotumors as a differential diagnosis in patients with lesions involving the clivus presenting with a sudden onset of symptoms of dysphagia and dysphonia along with lower limb weakness when other more threatening causes have been excluded. IgG4-related inflammatory pseudotumors are etiologically enigmatic and unpredictable, and total resection might not be warranted. Glucocorticoids are usually the first line of treatment after diagnosis.
引用
收藏
页数:6
相关论文
共 50 条
  • [1] IgG4-related inflammatory pseudotumor of the brain parenchyma: a case report and literature review
    Zhang, Zhuqing
    Fu, Weiwei
    Wang, Minghui
    Niu, Lei
    Liu, Bin
    Jiao, Yingbin
    Liu, Xuejun
    ACTA NEUROLOGICA BELGICA, 2018, 118 (04) : 617 - 627
  • [2] IgG4-related inflammatory pseudotumor of the brain parenchyma: a case report and literature review
    Zhuqing Zhang
    Weiwei Fu
    Minghui Wang
    Lei Niu
    Bin Liu
    Yingbin Jiao
    Xuejun Liu
    Acta Neurologica Belgica, 2018, 118 : 617 - 627
  • [3] IgG4-related diseases involving pleura: a case report and literature review
    Zuo, Anli
    Liu, Xinyi
    Guo, Zihan
    Jiang, Yunxiu
    Lu, Degan
    FRONTIERS IN MEDICINE, 2023, 10
  • [4] Successful surgical management of an aggressive IgG4-related sclerosing esophageal inflammatory pseudotumor: a case report and review of literature
    Nguyen, Hoang
    Pham, Duc Huan
    Luong, Tuan Hiep
    JOURNAL OF CARDIOTHORACIC SURGERY, 2023, 18 (01)
  • [5] Successful surgical management of an aggressive IgG4-related sclerosing esophageal inflammatory pseudotumor: a case report and review of literature
    Hoang Nguyen
    Duc Huan Pham
    Tuan Hiep Luong
    Journal of Cardiothoracic Surgery, 18
  • [6] IgG4-related inflammatory pseudotumor involving the temporal bone disguised as meningioma: a case description and literature analysis
    Chen, Yuanyuan
    Li, Tao
    Wen, Dan
    Zhao, Zhenkai
    Tang, Yan
    QUANTITATIVE IMAGING IN MEDICINE AND SURGERY, 2023, 13 (02) : 1240 - 1247
  • [7] IgG4-related disease presenting with an epidural inflammatory pseudotumor: A case report
    Ferreira N.R.
    Vaz R.
    Carmona S.
    Mateus S.
    Pereira P.
    Fernandes L.
    Moreira H.
    Chorão M.
    Saldanha L.
    Carvalho A.
    Campos L.
    Journal of Medical Case Reports, 10 (1)
  • [8] IgG4-related abdominal inflammatory pseudotumor: case report and overview of the diagnosis
    Vetterli, D.
    Moehrlen, U.
    Bode, P.
    Janz, I
    Angst, R.
    Klein-Franke, A.
    SWISS MEDICAL WEEKLY, 2016, 146 : 44S - 44S
  • [9] IgG4-Related Pseudotumor in the Sinonasal Cavity: Presentation of a Case and Literature Review
    Vercauteren, Leonie
    Van Haesendonck, Gilles
    Van Offel, Steven
    Walschot, Mark
    Sirimsi, Sabriya
    Vroegop, Anneclaire V.
    Faris, Callum
    B-ENT, 2022, 18 (02) : 121 - 127
  • [10] IgG4-related Diaphragmatic Inflammatory Pseudotumor
    Tanaka, Yu
    Takikawa, Tetsuya
    Kume, Kiyoshi
    Kikuta, Kazuhiro
    Hamada, Shin
    Miura, Shin
    Yoshida, Naoki
    Hongo, Seiji
    Matsumoto, Ryotaro
    Sano, Takanori
    Ikeda, Mio
    Unno, Michiaki
    Masamune, Atsushi
    INTERNAL MEDICINE, 2021, 60 (13) : 2067 - 2074