Behçet’s disease physiopathology: a contemporary review View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2016-12

AUTHORS

Mohamad J. Zeidan, David Saadoun, Marlene Garrido, David Klatzmann, Adrien Six, Patrice Cacoub

ABSTRACT

Behçet's disease, also known as the Silk Road Disease, is a rare systemic vasculitis disorder of unknown etiology. Recurrent attacks of acute inflammation characterize Behçet's disease. Frequent oral aphthous ulcers, genital ulcers, skin lesions and ocular lesions are the most common manifestations. Inflammation is typically self-limiting in time and relapsing episodes of clinical manifestations represent a hallmark of Behçet's disease. Other less frequent yet severe manifestations that have a major prognostic impact involve the eyes, the central nervous system, the main large vessels and the gastrointestinal tract. Behçet's disease has a heterogeneous onset and is associated with significant morbidity and premature mortality. This study presents a current immunological review of the disease and provides a synopsis of clinical aspects and treatment options. More... »

PAGES

4

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s13317-016-0074-1

DOI

http://dx.doi.org/10.1007/s13317-016-0074-1

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1004746176

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/26868128


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