... had led to use complement inhibitor when systemic manifestations occur with a promising therapeutic result. Dermatopathology Immunology Skin inflammation Vasculitis Atrophic papulosis (AP), also known as Köhlmeier-Degos disease or Degos disease, is a rare obliterating vasculopathy...

..., water and alcohol). Moreover, we reviewed the cases of sparing phenomenon described in the literature. In conclusion this is the first report of a sparing phenomenon of purpuric lesions over tattooed skin. Tattoo Purpura Vasculitis Sparing phenomenon Koebner nonreaction Isomorphic nonresponse...

... identified. Three patients presented with necrotizing vasculitis and 2 with pyoderma gangrenosum. Chronic venous insufficiency was diagnosed as the underlying cause of leg ulcers in 8 patients, peripheral arterial disease in 4 patients, and combined arterial and venous malfunction in 3 patients. Five...

...J.C.M. Hendrikse; D. Suurmond; G. Smeenk A 42-year-old man with recurrent attacks of blue-black haemorrhages predominantly on the palms and soles is described. Histology of a lesion revealed typical signs of allergic vasculitis. Direct immunofluorescence showed IgG and complement depositions...

... characteristic of Behçet’s disease. 27 07 1973 5 09 1973 16 10 2009 Behçet’s disease Vasculitis Venous thrombosis Fibrinolysis © 1974 S. Karger AG, Basel 1974 Copyright / Drug Dosage / Disclaimer Copyright: All rights reserved. No part of this publication may be translated...

...Amir Tanay; Israel Yust; Sarah Brenner; Michael Koffler; Arie L. Abramov A 65-year-old patient developed nonpruritic purpuric skin eruptions following 10 days of coumadin treatment. Skin biopsy revealed vasculitis and immunofluorescent studies demonstrated the presence of IgM and C3 deposits...

...Yechezkel Sidi; Abraham Weinberger; Shlomo Berliner; Mina Ben-Bassat; Carlos Idesses; Elazar J. Feuerman; Jack Pinkhas The case of a patient with mixed-type cryoglobulinemia and cutaneous necrotizing vasculitis, who later suffered from relapsing polychondritis affecting the auricle and the nose...

...M. Stavorovsky; D. Lichtenstein; F. Nissim The appearance of petechiae and ecchymoses following anticoagulant and fibrinolytic therapy is an unusual and rare complication. The mechanism of the vasculitis is obscure but may be related to a chemical vasotoxic reaction. During anticoagulant...

... or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Sweet’s syndrome Elastase Polymorphonuclear leukocyte Vasculitis Arthus phenomenon Dermatologies 166: 181-185 (1983) © 1983 S. Karger AG, Basel 0011-9075/83/1664-0181 S 2.75/0...

...J. de Maubeuge; P. Reding; C. Tielemans; M. Dratwa; Y. Van Laethem; G. Achten 2 cases of cutaneous vasculitis associated with chronic hepatitis and mixed cryoglobulinaemia are reported. Further studies revealed in the first case hypocomplementaemia and glomerulonephritis. The cutaneous lesions...

...R. Werni; T. Schwarz; F. Gschnait A patient with clinically and histologically typical urticarial vasculitis has been treated with 0.5 mg of colchicine three times per day. This treatment resulted in both disappearance of urticarial skin lesions and amelioration of severe systemic symptoms...

... to in the content or advertisements. Henoch-Schönlein purpura Immunoglobulin A Circulating immune complexes Vasculitis Dermatológica 172: 245-253 (1986) © 1986 S. Karger AG. Basel 0011-9075/86/1725-0245 S 2.75/0 Value of the Assay for IgA-Containing Circulating Immune Complexes in Henoch-Schonlein...

...W.J. Boonk; C. Nieboer; P.C. Huijgens To analyze the role of immune complexes, complement activation and fibrinolysis in chronic urticaria (CU), we performed serological, immunohistochemical and histopathological studies in 20 patients. In addition, the relationship to urticarial vasculitis...

...Franco Vicario; J. Balparda; J.M. Santamaria; C. Alvaro; C. Arizaga; Miguel de la Villa; J.M. Arrinda; Fernandez Moral; A. Celada A patient suffering from brucellosis developed maculonodular and purpuric lesions. The skin biopsy showed granulomatous vasculitis with no deposition of immunoglobulins...

... to in the content or advertisements. Chronic meningococcemia Neisseria meningitidis Vasculitis Fever 8 10 2009 Swiss Society Proceedings 71st Annual Meeting of the Swiss Society for Dermatology and Venereology Zurich, September 15 and 16, 1989 71. Jahresversammlung der Schweizerischen...

...J.P.H. Drenth; J.J. Michiels; T. Van Joost; V.D. Vuzevski A 50-year-old female patient is described with an acquired, persisting and yet incurable erythermalgia featured by symmetric burning pain and red congestion of the extremities secondary to cutaneous vasculitis. A weakly positive antinuclear...

...L. Machet; L. Vaillant; M.C. Machet; M. Büchler; G. Lorette 6 10 2009 Schönlein-Henoch purpura Vasculitis Immunoglobulin A Helicobacter pylori References 1 Kolde G. Luger T, Sorg C. Sunderkôtter C: Successful treatment of cutaneous leishmaniasis using systemic interferon-gamma...

... the histopathologic changes in urticarial lesions, we reviewed 25 original biopsies from 15 cases of Schnitzler’s syndrome, 11 of which have previously been reported. Results: Thirteen specimens from 9 patients showed urticaria with neutrophils (neutrophilic urticaria). Necrotizing leukocytoclastic vasculitis...

...-treated ulcers. After a 4-week treatment, hydrocolloid-treated ulcers contained clumps of microorganisms and showed massive infiltration by phagocytes including Mac 387+ and factor XIIIa+ cells. Leukocytoclastic vasculitis was present as well. These features were less pronounced in ulcers treated...

...Sonja Grunewald; Marc Bodendorf; Melanie Maier; Jan-Christoph Simon; Uwe Paasch Scalp necrosis Giant cell arteritis Parietal region Vasculitis 8 10 2008 © 2006 S. Karger AG, Basel 2008 Copyright / Drug Dosage / Disclaimer Copyright: All rights reserved. No part...