Results 41 to 50 of about 2,648 (158)

Exploring the Vasculitis‐Tumors Link: Epidemiological Patterns, Mechanistic Insights, and Clinical Implications

open access: yesAdvanced Science, Volume 13, Issue 14, 9 March 2026.
This review outlines association between vasculitis and malignancies and provides practical value for clinicians in distinguishing primary vasculitis from malignancy‐associated forms and optimizing patient surveillance, improving recognition of tumor‐associated vasculitis to reduce the risk of misdiagnosis, supporting more accurate clinical decision ...
Xiaofei Shi   +8 more
wiley   +1 more source

Cutaneous Polyarteritis Nodosa [PDF]

open access: yesDer Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 2020
Florian, Kapp   +3 more
  +6 more sources

Chronic polyarthritis as the first manifestation of childhood systemic polyarteritis nodosa

open access: yesEinstein (São Paulo)
Arthritis has been reported as an acute pattern, generally evanescent with oligoarthritis, mostly affecting knees and ankles in childhood systemic polyarteritis nodosa.
Glaucia Vanessa Novak   +5 more
doaj   +1 more source

Diagnostic Implications and Correlates of Plasma Adenosine Deaminase 2 Activity and ADA2 Variants

open access: yesArthritis &Rheumatology, Volume 78, Issue 3, Page 734-742, March 2026.
Objective Deficiency of adenosine deaminase 2 (DADA2) is a monogenic autoinflammatory disease manifested as polyarteritis nodosa, stroke, and bone marrow failure. Leveraging an international cohort of 200 DADA2 cases, we aimed to characterize the diagnostic utility of a plasma ADA2 enzyme activity assay and understand the implications of residual ADA2 ...
Jian Yue   +55 more
wiley   +1 more source

A comprehensive review on pathogenesis, associations, clinical findings, and treatment of livedoid vasculopathy

open access: yesFrontiers in Medicine, 2022
Livedoid vasculopathy (LV) is a thrombo-occlusive vasculopathy that involves the dermal vessels. Clinically, it is characterized by the presence of painful purpuric ulcers on the lower extremities.
Mireia Seguí, Mar Llamas-Velasco
doaj   +1 more source

Clinical and Pathological Features of Vasculitic Neuropathy: A Single‐Center Study in China

open access: yesEuropean Journal of Neurology, Volume 33, Issue 3, March 2026.
Vasculitic neuropathy in mainland China predominantly presents as axonal sensorimotor neuropathy. Systemic VN shows more frequent transmural inflammatory infiltration, whereas EGPA is more common in cases without infiltration. Most treated patients achieved remission, and the overall prognosis was relatively favorable, underscoring the importance of ...
Xiaoyu Zhou   +9 more
wiley   +1 more source

Multiple Mononeuropathy Secondary to Parvovirus B19 Infection: A Case Series

open access: yesEuropean Journal of Neurology, Volume 33, Issue 3, March 2026.
Parvovirus B19 infection can cause multiple mononeuropathy in young and immunocompetent patients, predominantly affecting sensory nerves, with frequent involvement of the median, fibular, and ulnar nerves, as well as occasional cranial nerve impairment.
Julian Theuriet   +32 more
wiley   +1 more source

Olaparib‐associated cutaneous vasculitis in a patient with breast cancer

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Marcial Álvarez‐Salafranca   +3 more
wiley   +1 more source

An Atypical Case of Vasculitis: When ‘Occult’ 18FDG-PET Scan Findings Create a Classification Dilemma

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2019
We describe a 66-year old patient with a recurrent ulcer on her right ankle. Biopsy revealed medium-vessel vasculitis consistent with cutaneous polyarteritis nodosa.
Elena Lopez-Francos   +3 more
doaj   +1 more source

Cryoglobulinemia: An update on classification, pathophysiology, clinical presentation, and management

open access: yesJournal of Internal Medicine, Volume 299, Issue 2, Page 196-215, February 2026.
Abstract Cryoglobulinemia (CG) is defined by the presence of serum immunoglobulins that precipitate below 37°C and redissolve upon rewarming. It is classified into three types based on immunoglobulin composition. Type I, a rare form, involves monoclonal IgM or IgG and is linked to lymphoproliferative disorders.
Anna Linda Zignego   +7 more
wiley   +1 more source

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