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444 Possible Causes for Urticarial Vasculitis

  • Infectious Mononucleosis

    vasculitis Acrocyanosis (bluish hands and feet) Annular erythema Pityriasis lichenoides Palmar dermatitis Reactive genital ulceration Chronic bullous disease of childhood[] Not only morbilliform lesions, but in some cases urticarial, purpuric and vesicular rashes, pustular eyrthematous rash, universal erythema or cutaneous vasculitis in the erythema[] […] associated with EBV infection, including: Infantile papular acrodermatitis (Gianotti-Crosti syndrome ) Erythema multiforme Erythema nodosum Urticaria including cold urticaria Urticarial[]

  • Urticaria

    Matthew Zirwas presented a lecture on The Urticarial Spectrum – Chronic Urticaria, Urticarial Vasculitis, Urticarial Dermatitis, Contact Urticaria, and Physical Urticarias[] Urticarial vasculitis, contact urticaria, and special syndromes are also included under the broad heading of urticaria.[] vasculitis[]

  • Schnitzler Syndrome

    Both urticarial vasculitis and Schnitzler syndrome are serious diseases but a recently gained better understanding of their underlying pathomechanism allows better treatment[] However, hypocomplementic urticarial vasculitis, systemic lupus erythematosus, cryoglobulinemia, acquired C1 inhibitor deficiency, hyper IgD syndrome, chronic infantile neurologic[] Schnitzler syndrome A clinical condition characterised by the association of IgM gammopathy and urticarial vasculitis.[]

  • Hypocomplementemic Vasculitis

    Hypocomplementemic vasculitis Unusual lupus-like syndrome Mac Duffie syndrome Anti-C1q vasculitis edit English Urticarial vasculitis No description defined Chronic urticaria[] Urticarial vasculitis (also known as "chronic urticaria as a manifestation of venulitis", "hypocomplementemic urticarial vasculitis syndrome", "hypocomplementemic vasculitis[] Sasaki T, Yonemasu K, Matsumoto M, Nagaki K: Characterization of C1q found in a patient with hypocomplementemic vasculitis-urticaria syndrome .[]

  • Vasculitis

    Conclusion: Hypocomplementaemic urticarial vasculitis constitutes a rare, but not always benign condition.[] To the best of our knowledge, we report the first case of deferasirox-induced urticarial vasculitis.[] Objectives: The aim was to describe the clinical characteristics and epidemiology of hypocomplementaemic urticarial vasculitis (HUV; anti-C1q vasculitis) in two geographically[]

  • Nonallergic Urticaria

    What is urticarial vasculitis? Urticarial vasculitis differs from urticaria in that the wheals tend to last longer than 24 hours.[] Urticarial vasculitis showing fixed urticarial plaques and hemosiderin patches. Image courtesy of Logical Images, Inc.[] Steroids may also be used in urticarial vasculitis, which usually does not respond to antihistamines.[]

  • Hepatitis B

    Hepatitis B is a form of viral hepatitis, caused by the hepatitis B virus, a member of the Hepadnavirus family. It is estimated that worldwide, more than 350 million people have chronic hepatitis B virus infection. The course of the disease may be extremely variable, depending on the patient’s age and immune status.[…][]

  • Systemic Vasculitis

    The serum levels of sVE-cadherin in 30 patients with HSP, together with patients with urticarial vasculitis, allergic vasculitis, Behcet disease, psoriasis vulgaris (PV) and[] , hypocomplementemic urticarial vasculitis, and Takayasu arteritis.[] […] renal involvement, two with Behçet's disease, three with urticarial vasculitis, one with primary cerebral vasculitis, one with relapsing polychondritis and one with IgA vasculitis[]

  • Cutaneous Leukocytoclastic Vasculitis

    Sixteen cases were classified as urticarial vasculitis based on the major clinical manifestations, while the remaining 28 cases represented various patterns.[] urticarial vasculitis — a group of cutaneous vasculitides characterized by urticaria lasting longer than 24 hours.[] […] edema of infancy Urticarial vasculitis Cryoglobulinemic vasculitis Erythema elevatum diutinum Granuloma faciale ANCA-associated vasculitis [11] Arthropod bites [11] Platelet[]

  • Serum Sickness

    Exanthematous drug eruption Hereditary angioedema Erythema multiforme Mononucleosis Urticarial vasculitis Henoch-Schönlein purpura Cellulitis Erythema infectiosum Best Tests[] Vasculitis Urticaria multiforme Acute hemorrhagic edema of infancy DRESS syndrome Evaluation If your suspicion for a drug reaction – either serum sickness or serum sickness-like[] However immunecomplexes, hypocomplementemia, vasculitis, and renal lesions are absent in SSLR [9].[]

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