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本文引用的文献

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Rituximab therapy leads to rapid decline of serum IgG4 levels and prompt clinical improvement in IgG4-related systemic disease.利妥昔单抗治疗可导致血清IgG4水平迅速下降,并使IgG4相关系统性疾病的临床症状迅速改善。
Arthritis Rheum. 2010 Jun;62(6):1755-62. doi: 10.1002/art.27435.
2
A case of paranasal sinus lesions in IgG4-related sclerosing disease.1例IgG4相关性硬化性疾病累及鼻窦的病例。
Otolaryngol Head Neck Surg. 2010 Mar;142(3):458-9. doi: 10.1016/j.otohns.2009.09.019. Epub 2009 Nov 25.
3
Nasal cavity neoplasms: a pictorial review.
Curr Probl Diagn Radiol. 2010 Mar-Apr;39(2):54-61. doi: 10.1067/j.cpradiol.2009.07.001.
4
Pituitary and stalk lesions (infundibulo-hypophysitis) associated with immunoglobulin G4-related systemic disease: an emerging clinical entity.与免疫球蛋白 G4 相关的系统性疾病相关的垂体和柄部病变(漏斗垂体炎):一种新兴的临床实体。
Endocr J. 2009;56(9):1033-41. doi: 10.1507/endocrj.k09e-277. Epub 2009 Nov 19.
5
Multiple IgG4-related sclerosing lesions in the maxillary sinus, parotid gland and nasal septum.上颌窦、腮腺和鼻中隔的多发IgG4相关性硬化性病变。
Pathol Int. 2009 Sep;59(9):670-5. doi: 10.1111/j.1440-1827.2009.02425.x.
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IgG4-related Sclerosing disease: a potential new etiology of cutaneous pseudolymphoma.IgG4相关性硬化性疾病:皮肤假性淋巴瘤的一种潜在新病因。
Am J Surg Pathol. 2009 Nov;33(11):1713-9. doi: 10.1097/PAS.0b013e3181b201de.
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Presentation and management of post-treatment relapse in autoimmune pancreatitis/immunoglobulin G4-associated cholangitis.自身免疫性胰腺炎/免疫球蛋白G4相关性胆管炎治疗后复发的表现与管理
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Proposal for a new clinical entity, IgG4-positive multiorgan lymphoproliferative syndrome: analysis of 64 cases of IgG4-related disorders.关于一种新的临床实体——IgG4阳性多器官淋巴增殖综合征的提议:对64例IgG4相关疾病的分析
Ann Rheum Dis. 2009 Aug;68(8):1310-5. doi: 10.1136/ard.2008.089169. Epub 2008 Aug 13.
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A case of IgG4-related multifocal fibrosclerosis complicated by central diabetes insipidus.1例IgG4相关性多灶性纤维化合并中枢性尿崩症。
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Reactive lymphoid follicular hyperplasia mimicking a peripheral nerve tumor.
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免疫球蛋白 G4 相关硬化性疾病模拟鼻腔和鼻窦侵袭性肿瘤。

Immunoglobulin G4-related sclerosing disease mimicking invasive tumor in the nasal cavity and paranasal sinuses.

机构信息

Department of Radiology, Asahikawa Medical University, Hokkaido, Japan.

出版信息

AJNR Am J Neuroradiol. 2012 Feb;33(2):E19-20. doi: 10.3174/ajnr.A2495. Epub 2011 May 5.

DOI:10.3174/ajnr.A2495
PMID:21546462
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7964793/
Abstract

IgG4RSD affecting the nasal cavity and paranasal sinuses is extremely rare. A 71-year-old man presented with an invasive mass in the nasal cavity and paranasal sinuses that was confirmed by immunostaining to be IgG4RSD. The occurrence of this disease in the nasal cavity and paranasal sinuses can resemble a malignant tumor on diagnostic imaging.

摘要

IgG4 相关蝶窦炎(IgG4-related sclerosing disease,IgG4RSD)累及鼻腔和鼻窦极为罕见。我们报告了一例 71 岁男性患者,其鼻腔和鼻窦内有侵袭性肿块,免疫组化染色证实为 IgG4RSD。该病在鼻腔和鼻窦的发生在影像学诊断上可类似恶性肿瘤。