Suppr超能文献

纤维蛋白性涎腺管炎(库斯莫尔病):3例报告及文献复习

Sialodochitis fibrinosa (kussmaul disease) report of 3 cases and literature review.

作者信息

Flores Robles Bryan Josue, Brea Álvarez Beatriz, Sanabria Sanchinel Abel Alejandro, Andrus Robert Francis, Espinosa Malpartida María, Ramos Giráldez Consuelo, Lerma Verdejo Ana, Merino Argumanez Carolina, Pérez Pimiento Jose Antonio, Bellas Menéndez Camen, Villa Alcázar Luis Fernando, Andréu Sánchez José Luis, Jiménez Palop Mercedes, Godoy Tundidor Hildegarda, Campos Esteban José, Sanz Sanz Jesús, Barbadillo Mateos Carmen, Isasi Zaragoza Carlos María, Mulero Mendoza Juan Bartolomé

机构信息

Rheumatology Division Radiodiagnostic Division, Puerta de Hierro Hospital, Madrid Neurology Division, Lozano Blesa Hospital, Zaragoza, Spain Independence Polyclinic, Belize Haematology Division Allergology Division Anatomical Pathology Division, Puerta de Hierro Hospital, Madrid, Spain.

出版信息

Medicine (Baltimore). 2016 Oct;95(42):e5132. doi: 10.1097/MD.0000000000005132.

Abstract

BACKGROUND

Sialodochitis fibrinosa is a rare disease which is characterized by recurring episodes of pain and swelling of the salivary glands due to the formation of mucofibrinous plugs. Analytic studies ascertain elevated levels of eosinophils and immunoglobulin E (IgE). Imaging studies such as magnetic resonance imaging (MRI) and sialography reveal dilation of the main salivary duct (duct ectasia). Treatment is initially supportive, consisting of compressive massages, and use of antihistamines and/or corticosteroids.

MATERIAL AND METHODS

In the following, 3 cases of sialodochitis fibrinosa are presented which were diagnosed in a third level hospital during the period of 2008 and 2016, as well as a literature review of all cases reported to our knowledge.

RESULTS

Of the 41 cases found, including the 3 of this article, 66% were women with an average age of 45 years old. However, 75% of reported cases were of Japanese heritage. Involvement of the parotid glands was more frequent than the submandibular glands. In more than half of all cases treatment with compressive massages, antihistamines and/or corticosteroids was effective.

CONCLUSION

Clinicians should consider sialodochitis fibrinosa as a diagnostic possibility when presented with cases of recurring parotid and submandibular gland tumescence.

摘要

背景

纤维蛋白性涎管炎是一种罕见疾病,其特征是由于黏液纤维蛋白性栓子形成导致唾液腺反复出现疼痛和肿胀。分析研究确定嗜酸性粒细胞和免疫球蛋白E(IgE)水平升高。磁共振成像(MRI)和涎管造影等影像学研究显示主涎管扩张(导管扩张)。治疗初期以支持治疗为主,包括压迫性按摩以及使用抗组胺药和/或皮质类固醇。

材料与方法

以下介绍了2008年至2016年期间在一家三级医院诊断出的3例纤维蛋白性涎管炎病例,并对我们所知的所有报告病例进行了文献综述。

结果

在找到的41例病例中,包括本文的3例,66%为女性,平均年龄45岁。然而,75%的报告病例有日本血统。腮腺受累比下颌下腺更常见。在超过一半的病例中,采用压迫性按摩、抗组胺药和/或皮质类固醇治疗有效。

结论

当遇到腮腺和下颌下腺反复肿大的病例时,临床医生应考虑纤维蛋白性涎管炎的诊断可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a661/5079326/c76beccb3df4/medi-95-e5132-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验