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IgG4相关性慢性鼻-鼻窦炎:一种鼻腔疾病的新临床实体。

IgG4-related chronic rhinosinusitis: a new clinical entity of nasal disease.

作者信息

Moteki Hideaki, Yasuo Masanori, Hamano Hideaki, Uehara Takeshi, Usami Shin-ichi

机构信息

Department of Otorhinolaryngology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Japan.

出版信息

Acta Otolaryngol. 2011 May;131(5):518-26. doi: 10.3109/00016489.2010.533699. Epub 2010 Dec 16.

Abstract

CONCLUSION

IgG4-related disease involves nasal manifestations with chronic rhinosinusitis (CRS). This type of sinusitis is a new clinical entity of nasal disease associated with a high level of serum IgG4 for which steroid therapy is effective. Objectives. To confirm whether IgG4-related disease has distinctive chronic rhinosinusitis.

METHODS

We compared serum IgG4 levels as well as nasal computed tomography (CT) and clinicopathological findings before and after glucocorticoid treatment in 31 patients diagnosed as having IgG4-related disease with nasal manifestations. To evaluate immunohistochemical findings of nasal mucosa, we compared them with IgG4-related CRS and common CRS.

RESULTS

All patients had levels of high serum IgG4. Ten of the 31 patients had nasal obstruction, nasal discharge, postnasal discharge, hyposmia, and dull headache. They also demonstrated sinus lesions on radiological findings. After glucocorticoid treatment, serum IgG and IgG4 levels were markedly decreased and along with improvement of the symptoms, nasal sinus CT findings also revealed improvement of the sinus opacification. In immunohistochemical examination, the magnitude of IgG4-positive plasma cell infiltration in common CRS was almost the same as in the IgG4-related CRS group. Therefore, in nasal mucosa immunocytochemical positive staining for IgG4 is not specific for definition of IgG4-related disease.

摘要

结论

IgG4相关性疾病累及鼻部表现,伴有慢性鼻窦炎(CRS)。此类鼻窦炎是一种与高水平血清IgG4相关的鼻部疾病新临床实体,糖皮质激素治疗有效。目的:确认IgG4相关性疾病是否具有独特的慢性鼻窦炎。

方法

我们比较了31例诊断为有鼻部表现的IgG4相关性疾病患者在糖皮质激素治疗前后的血清IgG4水平、鼻窦计算机断层扫描(CT)及临床病理结果。为评估鼻黏膜的免疫组化结果,我们将其与IgG4相关性CRS和普通CRS进行了比较。

结果

所有患者血清IgG4水平均高。31例患者中有10例出现鼻塞、流涕、后鼻滴涕、嗅觉减退及钝痛。影像学检查也显示鼻窦病变。糖皮质激素治疗后,血清IgG和IgG4水平明显降低,随着症状改善,鼻窦CT结果也显示鼻窦混浊有所改善。在免疫组化检查中,普通CRS中IgG4阳性浆细胞浸润程度与IgG4相关性CRS组几乎相同。因此,在鼻黏膜中,IgG4免疫细胞化学阳性染色对定义IgG4相关性疾病并不特异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb67/3490482/2a7bc1b799ca/OTO-131-0518-g001.jpg

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