Zobrazeno 1 - 10
of 1 169
pro vyhledávání: '"Urticarial vasculitis"'
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Urticarial vasculitis (UV) is a type III hypersensitivity reaction, characterized by immune complex deposition in small vessels leading to complement activation. Hypocomplementemic urticarial vasculitis syndrome (HUVS) represents the most severe form
Externí odkaz:
https://doaj.org/article/058ffa14fff74d51a4d9f020b27cab8d
Autor:
Sarah Benarab, Aurélien Chepy, Fréderic Dezoteux, Selma Azib, Eric Hachulla, David Launay, Marie Verhasselt‐Crinquette, Sébastien Sanges, Delphine Staumont‐Sallé
Publikováno v:
JEADV Clinical Practice, Vol 3, Iss 1, Pp 169-181 (2024)
Abstract Background As there are no definite classification criteria for urticarial vasculitis (UV), its diagnosis is often challenging and usually proposed when urticarial lesions and pathological vasculitis coexist. By analysing the final diagnosis
Externí odkaz:
https://doaj.org/article/b0bf1bbe1dfe46c581af0b2a96581997
Akademický článek
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Autor:
Daisuke Kawakami, Yoshiko Oda, Yumi Oka, Anri Morita, Keiko Kuroda, Yoji Hirai, Chikako Nishigori, Atsushi Fukunaga
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 6, Iss 5, Pp 172-174 (2023)
Abstract An 81‐year‐old Japanese man presented with a history of recurrent eyelid swelling and purpura on the face, neck, and limbs. Because the initial clinical presentation was angioedema alone, the patient was treated with an H1‐receptor ant
Externí odkaz:
https://doaj.org/article/f9ceb14978f44a36b9245efb9306d238
Autor:
Elena Juganaru, Claudia Cobilinschi, Ciprian Jurcut, Andreea Birlez, Daniela Opris-Belinski, Andra Balanescu
Publikováno v:
Romanian Journal of Rheumatology, Vol 32, Iss 1, Pp 35-38 (2023)
Sjogren’s syndrome (SSj) is a chronic autoimmune disease mainly targeting the exocrine glands, but sometimes associating extra-glandular manifestations. Xerosis, purpura, Raynaud’s phenomenon, cutaneous vasculitis, annular erythema are the main f
Externí odkaz:
https://doaj.org/article/24ed9a81f6b740af8de3f3ea224fa0a8
Autor:
Peter A. Young, MPAS, Atif Saleem, DO, Saisindhu Narala, MD, Allison Dear, BS, Gordon H. Bae, MD
Publikováno v:
JAAD Case Reports, Vol 28, Iss , Pp 138-141 (2022)
Externí odkaz:
https://doaj.org/article/8350a9c902444ae39eb7dbddba531783
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-5 (2022)
Abstract Background Urticarial vasculitis is a clinicopathologic entity defined by recurrent episodes of urticarial lesions that persist > 24 hours and demonstrate the histopathologic features of leukocytoclastic vasculitis. The most important progno
Externí odkaz:
https://doaj.org/article/03a9069537cb48058d58864eb36b2cf9
Publikováno v:
Frontiers in Allergy, Vol 4 (2023)
Externí odkaz:
https://doaj.org/article/20c5a6595eb4460dab8171c2c91f51c3
Autor:
Alice Corthier, Marie Jachiet, Daniel Bertin, Aude Servais, Christelle Barbet, Adrien Bigot, Marie-Sylvie Doutre, Didier Bessis, Ancuta Bouffandeau, Olivier Moranne, Pierre-André Jarrot, Nathalie Bardin, Benjamin Terrier, Stephane Burtey, Xavier Puéchal, Laurent Daniel, Noémie Jourde-Chiche
Publikováno v:
BMC Nephrology, Vol 23, Iss 1, Pp 1-12 (2022)
Abstract Background Hypocomplementemic urticarial vasculitis (HUV) is a rare systemic vasculitis. We aimed to describe the kidney involvement of HUV in a multicenter national cohort with an extended follow-up. Methods All patients with HUV (internati
Externí odkaz:
https://doaj.org/article/a47ebc38314743829b9a693ba7d5459b
Autor:
Joana Marques, Tiago Pereira, Dulce Carvalho, Mário Góis, Helena Sousa, Francisco Ribeiro, Fernando Nolasco
Publikováno v:
Revista Portuguesa de Nefrologia e Hipertensão, Vol 35, Iss 4, Pp 254-259 (2021)
Membranoproliferative glomerulonephritis describes a glomerular-injury pattern common to a heterogeneous group of diseases. Evaluation based on clinical and laboratory presentation and immunofluorescence staining on kidney biopsy allows identificatio
Externí odkaz:
https://doaj.org/article/8ea4b556b83348028b6edeeaaa2e5f33