igg4相关的硬化性疾病引起脊髓压迫:文献中首次报道的病例

Pub Date : 2019-06-18 DOI:10.1155/2019/3618510
Nooraldin Merza, A. Taha, J. Lung, Anthony W. Benderman, S. Wright
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引用次数: 8

摘要

免疫球蛋白g4相关疾病(IgG4-RD)以形成可能具有压缩作用的软组织肿块病变而闻名。这是一种非常罕见的疾病,最常影响胰腺引起自身免疫性胰腺炎。它也可以影响胆囊、唾液腺和泪腺,引起相应的器官特异性并发症。在我们的报告中,我们描述了一个影响脊髓的IgG4-RD病例。一名60岁女性,因IgG4-RD引起颈脊髓受压,导致多种神经功能缺损。肿块切除活检病理检查显示淋巴浆细胞浸润致密,间质纤维化伴IgG4和浆细胞。患者对全身性类固醇治疗有显著反应,神经系统症状几乎消失。本病例是文献中第一例硬膜外组织IgG4-RD引起脊柱压迫的病例。因此,我们也证明了IgG4-RD对全体性类固醇治疗的显著反应,因为患者在5年的密切随访后没有复发,这是迄今为止文献中报道的最长的随访期。
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IgG4-Related Sclerosing Disease Causing Spinal Cord Compression: The First Reported Case in Literature
Immunoglobulin G4-related disease (IgG4-RD) is known for forming soft tissue mass lesions that may have compressive effects. It is an extremely rare disease that most frequently affects the pancreas causing autoimmune pancreatitis. It can also affect the gallbladder, salivary glands, and lacrimal glands causing respective organ-specific complications. In our report, we describe an IgG4-RD case that affected the spinal cord. A 60-year-old female presented with cervical spinal cord compression caused by IgG4-RD leading to several neurological deficits. Pathological examination of the excisional biopsy of the mass revealed dense lymphoplasmacytic cells infiltration and stromal fibrosis with IgG4 and plasma cells. The patient showed a dramatic response to the administration of systemic steroids with almost resolution of her neurological symptoms. This case highlights the first case in literature for IgG4-RD of the extradural tissue causing spinal compression. Hereby, we also demonstrate the dramatic response of IgG4-RD to the administration of systemic steroids as the patient had no recurrence after 5 years of close follow-up, the longest reported period of follow-up reported in the literature to date.
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