Results 61 to 70 of about 8,981 (257)
Cryptococcid Sweet Syndrome in the Setting of Hydralazine‐Induced ANCA Vasculitis: A Case Report
Journal of Cutaneous Pathology, EarlyView.ABSTRACT Acute febrile neutrophilic dermatosis, also known as Sweet syndrome, is an inflammatory skin condition characterized by the rapid onset of painful, erythematous plaques or nodules with neutrophilic infiltrate on histology. Rarely, acellular bodies surrounded by vacuolated spaces have been noted within the neutrophilic infiltrate, mimicking ...
Jenna Vroman +4 more
wiley +1 more source
Fulminant Wegener's granulomatosis: A case report [PDF]
, 2013 Introduction. Granulomatosis Wegener is anti-neutrophil cytoplasmic antibodies (ANCAs)-associated systemic vasculitis of unknown etiology. It is manifested as granulomatous necrotizing inflammation of the upper and lower parts of the respiratory tract,
Dinić Miroslav Ž. +3 more
core +1 more source
Immunology, EarlyView.A constant rate of DNA damage that is not perfectly repaired will cause a constant rate of DNA mutations. The chance of mutation will increase if DNA is prone to damage, such as occurs in somatic hypermutation (SHM) hotspots and GC‐rich DNA. Thus, if one mutation‐prone DNA site drives disease, the age of onset of disease and degree of penetrance should
Piet C. de Groen
wiley +1 more source
Methimazole-Induced Leukocytoclastic Vasculitis: A Case Report
Case Reports in Dermatology, 2019 Major identifiable causes of leukocytoclastic vasculitis include certain infections and medications. Amongst antithyroid drugs, methimazole (MMI) is rarely implicated as a culprit drug.
Weeratian Tawanwongsri +1 more
doaj +1 more source
Immunological deep dermal vasculitis in a cat [PDF]
, 2014 In this case report, a 13.5-year-old, neutered, female domestic shorthaired cat with immunological deep dermal vasculitis is described. The patient was presented with lethargy, fever, polydipsia, anorexia and swollen distal limbs.
Daminet, Sylvie +3 more
core +1 more source
A 47-Year-Old Female with Shortness of Breath [PDF]
, 2012 This patient is a 47-year-old female with a history of end-stage liver disease secondary to hepatitis C virus (HCV) complicated by hepatic encephalopathy, obstructive sleep apnea, asthma, and severe peripheral neuropathy who presents to the hospital with
Marrero, MD, Dana, Wright, MD, Kelly
core +2 more sources
Successful Treatment of Severe Purpura Fulminans With Anakinra
Pediatric Dermatology, EarlyView.ABSTRACT Purpura fulminans (PF) is a rare, often fatal pediatric condition characterized by intravascular thrombosis and hemorrhagic infarction of the skin. A timely diagnosis and treatment are paramount to prevent the involvement of internal organs, causing disseminated intravascular coagulation and gangrene of the extremities.
Francesco Zulian +4 more
wiley +1 more source
Propylthiouracil-induced cutaneous vasculitis [PDF]
, 2008 The use of propylthiouracil (PTU) is associated with the development of different auto-antibodies, amongst them are antineutrophil cytoplasmic antibodies (ANCA) that are involved in the pathogenesis of ANCA associated systemic vasculitis.
Costa, Leonardo Atem Gonçalves A. +4 more
core +2 more sources
Dabigatran-related leukocytoclastic vasculitis [PDF]
BMJ Case Reports, 2017 Dabigatran is a non-vitamin K antagonist oral anticoagulant that has been approved for atrial fibrillation and prevention of venous thromboembolism. Its use has been increasing in the USA since serum drug levels do not need monitoring. To date, no significant skin side effects have been reported other than 4 cases of non-specific skin lesion and 2 ...
Josiah, An +3 more
openaire +2 more sources
Case Reports in Dentistry, Volume 2026, Issue 1, 2026.Introduction Granulomatosis with polyangiitis (GPA), formerly known as Wegener′s granulomatosis, is a rare, systemic small‐vessel vasculitis characterized by necrotizing granulomatous inflammation. It classically affects the upper airway, lungs, and kidneys.
Sarwer Biplob +4 more
wiley +1 more source