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Sialodochitis fibrinosa (kussmaul disease) report of 3 cases and literature review
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 ma...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079326/ https://www.ncbi.nlm.nih.gov/pubmed/27759642 http://dx.doi.org/10.1097/MD.0000000000005132 |
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author | Robles, Bryan Josue Flores Álvarez, Beatriz Brea Sanchinel, Abel Alejandro Sanabria Andrus, Robert Francis Malpartida, María Espinosa Giráldez, Consuelo Ramos Verdejo, Ana Lerma Argumanez, Carolina Merino Pimiento, Jose Antonio Pérez Menéndez, Camen Bellas Alcázar, Luis Fernando Villa Sánchez, José Luis Andréu Palop, Mercedes Jiménez Tundidor, Hildegarda Godoy Esteban, José Campos Sanz, Jesús Sanz Mateos, Carmen Barbadillo Zaragoza, Carlos María Isasi Mendoza, Juan Bartolomé Mulero |
author_facet | Robles, Bryan Josue Flores Álvarez, Beatriz Brea Sanchinel, Abel Alejandro Sanabria Andrus, Robert Francis Malpartida, María Espinosa Giráldez, Consuelo Ramos Verdejo, Ana Lerma Argumanez, Carolina Merino Pimiento, Jose Antonio Pérez Menéndez, Camen Bellas Alcázar, Luis Fernando Villa Sánchez, José Luis Andréu Palop, Mercedes Jiménez Tundidor, Hildegarda Godoy Esteban, José Campos Sanz, Jesús Sanz Mateos, Carmen Barbadillo Zaragoza, Carlos María Isasi Mendoza, Juan Bartolomé Mulero |
author_sort | Robles, Bryan Josue Flores |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5079326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-50793262016-11-03 Sialodochitis fibrinosa (kussmaul disease) report of 3 cases and literature review Robles, Bryan Josue Flores Álvarez, Beatriz Brea Sanchinel, Abel Alejandro Sanabria Andrus, Robert Francis Malpartida, María Espinosa Giráldez, Consuelo Ramos Verdejo, Ana Lerma Argumanez, Carolina Merino Pimiento, Jose Antonio Pérez Menéndez, Camen Bellas Alcázar, Luis Fernando Villa Sánchez, José Luis Andréu Palop, Mercedes Jiménez Tundidor, Hildegarda Godoy Esteban, José Campos Sanz, Jesús Sanz Mateos, Carmen Barbadillo Zaragoza, Carlos María Isasi Mendoza, Juan Bartolomé Mulero Medicine (Baltimore) 6900 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. Wolters Kluwer Health 2016-10-21 /pmc/articles/PMC5079326/ /pubmed/27759642 http://dx.doi.org/10.1097/MD.0000000000005132 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 6900 Robles, Bryan Josue Flores Álvarez, Beatriz Brea Sanchinel, Abel Alejandro Sanabria Andrus, Robert Francis Malpartida, María Espinosa Giráldez, Consuelo Ramos Verdejo, Ana Lerma Argumanez, Carolina Merino Pimiento, Jose Antonio Pérez Menéndez, Camen Bellas Alcázar, Luis Fernando Villa Sánchez, José Luis Andréu Palop, Mercedes Jiménez Tundidor, Hildegarda Godoy Esteban, José Campos Sanz, Jesús Sanz Mateos, Carmen Barbadillo Zaragoza, Carlos María Isasi Mendoza, Juan Bartolomé Mulero Sialodochitis fibrinosa (kussmaul disease) report of 3 cases and literature review |
title | Sialodochitis fibrinosa (kussmaul disease) report of 3 cases and literature review |
title_full | Sialodochitis fibrinosa (kussmaul disease) report of 3 cases and literature review |
title_fullStr | Sialodochitis fibrinosa (kussmaul disease) report of 3 cases and literature review |
title_full_unstemmed | Sialodochitis fibrinosa (kussmaul disease) report of 3 cases and literature review |
title_short | Sialodochitis fibrinosa (kussmaul disease) report of 3 cases and literature review |
title_sort | sialodochitis fibrinosa (kussmaul disease) report of 3 cases and literature review |
topic | 6900 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079326/ https://www.ncbi.nlm.nih.gov/pubmed/27759642 http://dx.doi.org/10.1097/MD.0000000000005132 |
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