Results 121 to 130 of about 201,611 (277)

Negative association of the chemokine receptor CCR5 d32 polymorphism with systemic inflammatory response, extra-articular symptoms and joint erosion in rheumatoid arthritis [PDF]

, 2009
Introduction Chemokines and their receptors control immune cell migration during infections as well as in autoimmune responses. A 32 bp deletion in the gene of the chemokine receptor CCR5 confers protection against HIV infection, but has also been ...
Arnold, Sybille, Baerwald, Christoph, Burkhardt, Harald, Keyßer, Gernot, Pierer, Matthias, Rossol, Manuela, Wagner, Ulf   +6 more
core   +2 more sources

Wound, pressure ulcer, and burn guidelines (2023)―4: Guidelines for the management of connective tissue disease/vasculitis‐associated skin ulcers, third edition

The Journal of Dermatology, EarlyView.
Yoshihide Asano, Jun Asai, Takayuki Ishii, Yohei Iwata, Masanari Kodera, Chie Miyabe, Akihiko Uchiyama, Youichi Ogawa, Ken Okamura, Mari Kishibe, Yuta Koike, Yorihisa Kotobuki, Noriki Fujimoto, Takuya Miyagi, Yukie Yamaguchi, Ayumi Yoshizaki, Reiko Omori, Takeshi Nakanishi, Hiroshi Fujiwara, Takeo Maekawa, Sei‐ichiro Motegi, Yuichiro Yoshino, Minoru Hasegawa, Manabu Fujimoto, Takao Tachibana, Wound, Pressure Ulcer, and Burn Guidelines Drafting Committee (connective tissue disease/vasculitis group)   +27 more
wiley   +1 more source

Clinical Signs, Advanced Diagnostic Imaging Findings, Treatment, and Outcome of Mycotic Discospondylitis in 11 Dogs

Journal of Veterinary Internal Medicine, Volume 39, Issue 3, May/June 2025.
ABSTRACT Background Discospondylitis refers to inflammation of the intervertebral disc and adjacent vertebral endplates. The literature on mycotic discospondylitis (MD) in dogs is limited. Objective To describe clinical and advanced diagnostic imaging findings, therapeutic strategies, and outcomes in dogs with a confirmed diagnosis of MD.
Samuel Okonji, Andrea Di Paola, Silvia Benini, Antonella Gallucci, Alberto Cauduro, Cristian Falzone, Teresa Gagliardo, Gualtiero Gandini   +7 more
wiley   +1 more source

Use of Plasmapheresis and Immunosuppressants to Treat Diffuse Alveolar Hemorrhage in a Patient with Granulomatosis with Polyangiitis. [PDF]

, 2019
Granulomatosis with polyangiitis (GPA) is a systemic granulomatous inflammatory disease characterized by small-to-medium vessel vasculitis due to Central Anti-Neutrophil Cytoplasmic Antibody (C-ANCA).
Sattar, Yasar, Susheela, Ammu Thampi, Ullah, Waqas, Usman, Norina, Zafrullah, Fnu   +4 more
core   +1 more source

Oxaliplatin-Induced Leukocytoclastic Vasculitis under Adjuvant Chemotherapy for Colorectal Cancer: Two Cases of a Rare Adverse Event [PDF]

, 2013
Leukocytoclastic vasculitis is a multicausal systemic inflammatory disease of the small vessels, histologically characterized by inflammation and deposition of both nuclear debris and fibrin in dermal postcapillary venules. The clinical picture typically
Conradi, Lena-Christin, Erpenbeck, Luise, Ghadimi, B. Michael, Liersch, Torsten, Michels, Beate, Middel, Peter, Neumann, Steffen, Quack, Henriette, Schaefer, Inga-Marie, Schön, Michael P., Seitz, Cornelia S., Sprenger, Thilo, Stanek, Kathrin, Wolff, Hendrik A.   +13 more
core   +2 more sources

Hospital-onset IgA vasculitis triggered by infectious endocarditis

IDCases, 2023
This is a case of IgA vasculitis developed in the hospital during treatment of infective endocarditis. When purpura appears in a patient under IE treatment, we should consider IgA vasculitis as a differential diagnosis and check renal function.
Kento Furuya, Naoya Itoh
doaj  

Autoantibodies in systemic vasculitis [PDF]

, 2015
Systemic vas culitis is a heterogeneous group of disorders characterized by inflammation and necrosis in the vessel wall. the diagnosis of a systemic vasculitis is challenging, because patients usually present a broad spectrum of manifestations that vary
Souza, Alexandre Wagner Silva de
core   +3 more sources

IgA vasculitis in an adult diabetic male with rapidly progressive glomerulonephritis: A case study

Journal of Acute Disease
Rationale: IgA vasculitis or Henoch-Schonlein purpura is an immune complex mediated small vessel vasculitis characterized by clinical triad of arthritis, palpable purpura and gastrointestinal symptoms.
Varsha Luthra, Aprajita Garg, Anjali Yadav, Tarun Chaudhary, Monica Gupta   +4 more
doaj   +1 more source

COVID19‐Related Onset and Relapses of Juvenile Systemic Lupus Erythematosus‐Like Disease

Journal of Paediatrics and Child Health, EarlyView.
Chiara Cannata, Francesca Tirelli, Alessandra Meneghel, Francesco Zulian   +3 more
wiley   +1 more source

A Case Report of Drug‐Induced Hemorrhagic Bullae

Clinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT Hemorrhagic bullae is a rare, non‐immune, cutaneous adverse reaction that happens after the administration of some medicine. This case is a unique report of vancomycin and alteplase‐induced hemorrhagic bullae and warns physicians and healthcare teams to take action properly.
Mehrdad Shavandi, Zohre Labbani‐Motlagh, Azin Abdollahi, Hadieh Tazerouni, Alireza Naserian, Shahideh Amini   +5 more
wiley   +1 more source