Langerhans Histiocytosis Renders a Differential and Complementary Diagnosis for a Sjögren Syndrome Female Presenting with a Hypophyseal Mass, Pulmonary Emphysema and Thyroid Nodules
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/article/10.1007/s12288-018-1016-z/fulltext.html
Reference5 articles.
1. Shiboski CH, Shiboski SC, Seror R et al (2017) 2016 American College of Rheumatology/European League Against Rheumatism classification criteria for primary Sjogren’s syndrome: a consensus and data-driven methodology involving three international patient cohorts. Ann Rheum Dis 76(1):9–16. https://doi.org/10.1136/annrheumdis-2016-210571
2. Caturegli P, Newschaffer C, Olivi A et al (2005) Autoimmune hypophysitis. Endocr Rev 26(5):599–614. https://doi.org/10.1210/er.2004-0011
3. Bellido-Casado J, Plaza V, Díaz C et al (2011) Bronchial inflammation, respiratory symptoms and lung function in Primary Sjögren’s syndrome. Arch Bronconeumol 47(7):330–334. https://doi.org/10.1016/j.arbres.2011.01.003
4. Shevale VV, Ekta K, Snehal T, Geetanjal M (2014) A rare occurrence of Langerhans cell histiocytosis in an adult. J Oral Maxillofac Pathol 18(3):415–419. https://doi.org/10.4103/0973-029X.151335
5. Patten DK, Wani Z, Tolley N (2012) Solitary langerhans histiocytosis of the thyroid gland: a case report and literature review. Head Neck Pathol 6(2):279–289. https://doi.org/10.1007/s12105-011-0321-8
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1. Radiological patterns and pulmonary function values of lung involvement in primary Sjögren’s syndrome: A pilot analysis;Frontiers in Medicine;2022-10-28
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