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胸椎旁肿块作为IgG4相关疾病的罕见表现

Thoracic Paravertebral Mass as an Infrequent Manifestation of IgG4-Related Disease.

作者信息

Matzumura Kuan Melissa, Rubin Bernard, Meysami Alireza

机构信息

Division of Rheumatology, Detroit Medical Center, Wayne State University, Henry Ford Hospital, Detroit, MI, USA.

Henry Ford Medical Group, Detroit, MI, USA.

出版信息

Case Rep Rheumatol. 2017;2017:4716245. doi: 10.1155/2017/4716245. Epub 2017 Dec 28.

Abstract

CASE

A 50-year-old African American male presented with abdominal pain and significant weight loss. On physical examination, he had parotid and submandibular gland enlargement associated with right eye proptosis. Computed tomography showed a thoracic paravertebral soft tissue mass, enlarged lymph nodes, and ascending aortic aneurysm. Laboratory results were remarkable for elevated total IgG and IgG4 subclass. The submandibular gland pathology revealed chronic sclerosing sialadenitis, with a large subset of inflammatory cells positively staining for IgG4. The histology of the paravertebral mass demonstrated fibrosclerosis with increased lymphocytic infiltrate, associated with increased IgG4 plasma cells. He was diagnosed with immunoglobulin G4-related disease (IgG4-RD). Steroid therapy initially yielded improvement; however, after steroids were stopped, there was disease recurrence. Prednisone was restarted, and the plan was to start him on rituximab. Interestingly, the patient's brother also had IgG4-RD.

CONCLUSION

IgG4-RD can present as a paravertebral mass which is usually responsive to steroids; however, recurrent and resistant disease can be seen for which steroid-sparing agents such as rituximab should be considered. In addition, to the best of our knowledge, this is the first reported case of IgG4-RD in two family members presenting as a paravertebral mass, highlighting an exciting area for more research in the future.

摘要

病例

一名50岁的非裔美国男性因腹痛和显著体重减轻前来就诊。体格检查发现,他有腮腺和颌下腺肿大,并伴有右眼突出。计算机断层扫描显示胸段椎旁软组织肿块、淋巴结肿大和升主动脉瘤。实验室检查结果显示总IgG和IgG4亚类升高。颌下腺病理显示为慢性硬化性涎腺炎,大量炎症细胞IgG4染色呈阳性。椎旁肿块的组织学表现为纤维硬化伴淋巴细胞浸润增加,伴有IgG4浆细胞增多。他被诊断为免疫球蛋白G4相关性疾病(IgG4-RD)。类固醇治疗最初取得了改善;然而,停用类固醇后,疾病复发。重新开始使用泼尼松,并计划让他开始使用利妥昔单抗。有趣的是,患者的兄弟也患有IgG4-RD。

结论

IgG4-RD可表现为椎旁肿块,通常对类固醇有反应;然而,可出现复发和耐药性疾病,对此应考虑使用利妥昔单抗等类固醇节省剂。此外,据我们所知,这是首次报道的两例家族成员均表现为椎旁肿块的IgG4-RD病例,突出了未来一个令人兴奋的更多研究领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/5763108/b055099f5a11/CRIRH2017-4716245.001.jpg

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