Results 121 to 130 of about 30,114 (242)

Microscopic Polyangiitis After Pulmonary Nontuberculous Mycobacterial Disease: A Case Report and Literature Review

open access: yesRespirology Case Reports, Volume 14, Issue 5, May 2026.
This case highlights that ANCA‐associated vasculitis can emerge in patients with chronic airway disease and a history of nontuberculous mycobacterial infection, potentially masquerading as infection‐related inflammation. Early recognition based on extrapulmonary clues (urinary abnormalities and neuropathy) enabled prompt diagnosis and treatment with ...
Hidenori Takahashi   +11 more
wiley   +1 more source

The pathogenesis of ANCA-associated vasculitis

open access: yesJapanese Journal of Clinical Immunology, 2016
ANCA-associated vasculitis is characterized by the presence of anti-neutrophil cytoplasmic antibody (ANCA) in the serum. ANCA is a pathogenic autoantibody as well as the disease marker. It has been realized that ANCA-cytokine sequence is involved in the pathogenesis of ANCA-associated vasculitis.
openaire   +3 more sources

Vasculitis por Propiltiouracilo: reporte de un caso

open access: yesActa Médica Costarricense, 2002
Se reporta el caso clínico de una paciente femenina de 43 años que presentó dos complicaciones secundarias al uso de propiltiouracilo: vasculitis y agranulocitosis.La vasculitis asociada con el tratamiento antitiroideo es una entidad clínica bien ...
Donato A. Salas-Segura   +2 more
doaj  

P-ANCA vasculitis in a patient with Alpha-1-Antitrypsin deficiency : a possible mechanism [PDF]

open access: yes, 2009
Antineutrophil cytoplasmic antibody (ANCA) testing plays a critical role in the diagnosis and classification of vasculitis. These antibodies are strongly associated with Wegener's granulomatosis, microscopic polyangiitis and Churg-Strauss syndrome ...
Tuffaha, Ahmad
core  

Fulminant Wegener's granulomatosis: A case report [PDF]

open access: yes, 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

Autoimmune‐Associated Pulmonary Inflammatory Myofibroblastic Tumour: A Diagnostic and Therapeutic Challenge

open access: yesRespirology Case Reports, Volume 14, Issue 5, May 2026.
Pulmonary inflammatory myofibroblastic tumour (IMT) is a rare neoplasm with variable behaviour, and its link to autoimmunity remains uncertain. We report a woman in her twenties with recurrent symptoms and radiological progression whose findings suggested autoimmune‐associated IMT, showing marked improvement with immunosuppressive therapy.
Ng Boon Hau   +7 more
wiley   +1 more source

Inflammation‐Driven Lymphoid Structures: Organization, Function, and Clinical Impact Across Autoimmunity, Cancer, and Checkpoint Toxicity

open access: yesImmunological Reviews, Volume 339, Issue 1, May 2026.
ABSTRACT Lymphoid structures (LS) arising in nonlymphoid tissues are increasingly recognized as active immune niches rather than simple consequences of chronic inflammation. In this review, we propose a framework that distinguishes inflammatory lymphoid structures (ILS) from mature tertiary lymphoid structures (mTLS), while acknowledging that these ...
Marie Frutoso   +6 more
wiley   +1 more source

Refractory ANCA-associated vasculitis [PDF]

open access: yesRheumatology, 2021
Seerapani Gopaluni   +3 more
openaire   +2 more sources

Evaluation of Acellular Intact Fish Skin Grafts for Treating Acute and Chronic Wounds

open access: yesInternational Wound Journal, Volume 23, Issue 5, May 2026.
ABSTRACT Acute, chronic, and hard‐to‐heal wounds pose a growing challenge due to reduced patient quality‐of‐life, higher cost and increased hospital admissions. Although there is no gold standard for wound care, there is a trend toward simple, outpatient‐compatible treatment options.
Christopher Böddeker   +4 more
wiley   +1 more source

Clinical significance of renal histological diagnosis in patients with type 2 diabetes and proteinuria atypical for diabetic nephropathy

open access: yesJournal of Diabetes Investigation, Volume 17, Issue 5, Page 781-790, May 2026.
ABSTRACT Background/Aim Most patients with proteinuria are considered to have typical diabetic nephropathy (DN). However, when proteinuria occurs without diabetic retinopathy, with hematuria, or persists despite strict glycemic and blood pressure control, it is considered atypical for DN and warrants further evaluation for non‐DN via kidney biopsy ...
Shogo Kuwagata   +16 more
wiley   +1 more source

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