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10.1097/MD.0000000000005132

http://scihub22266oqcxt.onion/10.1097/MD.0000000000005132
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C5079326!5079326!27759642
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suck abstract from ncbi


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pmid27759642      Medicine+(Baltimore) 2016 ; 95 (42): ä
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  • Sialodochitis fibrinosa (kussmaul disease) report of 3 cases and literature review #MMPMID27759642
  • Robles BJF; Álvarez BB; Sanchinel AAS; Andrus RF; Malpartida ME; Giráldez CR; Verdejo AL; Argumanez CM; Pimiento JAP; Menéndez CB; Alcázar LFV; Sánchez JLA; Palop MJ; Tundidor HG; Esteban JC; Sanz JS; Mateos CB; Zaragoza CMI; Mendoza JBM
  • Medicine (Baltimore) 2016[Oct]; 95 (42): ä PMID27759642show ga
  • 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.
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