Histopathologic picture of papulo-pustular cutaneous lesions (aphthae) in Behcet's syndrome

1974 ◽  
Vol 91 (s10) ◽  
pp. 27-28 ◽  
Author(s):  
J. Civatte ◽  
S. Belaich
2021 ◽  
Vol 8 ◽  
Author(s):  
Ina Kötter ◽  
Fabian Lötscher

Behçet‘s Syndrome (BS) is a variable vessel vasculitis according to the Chapel Hill Consensus Nomenclature (1) and may thus affect any organ, including major and minor arterial and venous vessels to a varying degree and with varying frequency. Although the main features of BS are recurrent oral and genital aphthous ulcers, cutaneous lesions, ocular inflammation and arthritis—major vessel and life—or organ threatening involvement of internal organs and the central and peripheral nervous system occur. In general, BS in Europe appears to form six phenotypes of clinical manifestations (2), which are (1) mucocutaneous only, (2) predominant arthritis/articular involvement, (3) vascular phenotype, (4) ocular manifestations, which are most likely associated with CNS manifestations and HLA-B51, (5) dominant parenchymal CNS manifestations (being associated with the ocular ones), and (6) gastrointestinal involvement. Mucocutaneous manifestations are present in almost all patients/all phenotypes. In the following review, we summarize the current knowledge concerning vascular, neurologic, gastrointestinal and musculoskeletal manifestations of the disease.


1970 ◽  
Vol 102 (1) ◽  
pp. 116-117 ◽  
Author(s):  
J. L. Fromer

1987 ◽  
Vol 28 (4) ◽  
pp. 291 ◽  
Author(s):  
Moon Soo Yoon ◽  
Seung Hun Lee ◽  
Dong Sik Bang ◽  
Sungnack Lee

2021 ◽  
Vol 77 (18) ◽  
pp. 2791
Author(s):  
Neiberg De Alcantara Lima ◽  
Henrique Carvalho Lima Farias ◽  
Ane Karoline Medina Neri ◽  
Danielli Lino ◽  
Isabela Thomáz Takakura Guedes ◽  
...  

2021 ◽  
pp. annrheumdis-2020-219810
Author(s):  
Jun Zou ◽  
Chen-Hong Lin ◽  
Yan Wang ◽  
Yan Shen ◽  
Jian-Long Guan

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