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A Case of IgG4-Related Disease Manifesting as Extensive Abdominal Periarteritis and Membranous Nephropathy, Successfully Controlled with Low-Dose Steroid Therapy without Relapse or Complications.
Nephron
November 2024
Department of Nephrology, Kyoto University, Kyoto, Japan.
Introduction: IgG4-related disease (IgG4-RD) is an immune-mediated fibroinflammatory disease that can affect nearly every organ system, including blood vessels and the kidney. IgG4-related vascular lesions mainly involve the aorta, and the dominant renal manifestation is tubulointerstitial nephritis (TIN). Here, we report a case of IgG4-RD demonstrating extensive abdominal periarteritis and membranous nephropathy (MN).
View Article and Find Full Text PDFRelationship between cutaneous polyarteritis nodosa (cPAN) and macular lymphocytic arteritis (MLA): Blinded histologic assessment of 35 cPAN cases.
J Am Acad Dermatol
December 2015
University Paris Diderot, Sorbonne Paris Cité, Assistance Publique des Hôpitaux de Paris (AP-HP), Dermatology, Pathology, and Internal Medicine Department, Saint Louis Hospital, Paris, France. Electronic address:
Background: Cutaneous polyarteritis nodosa (cPAN) is a skin medium vessel neutrophilic arteritis with livedo, nodules, and ulcerations. Macular lymphocytic arteritis (MLA) is a small arteritis with erythematous or pigmented macules and typical histologic features (a lymphocytic infiltrate, concentric fibrin ring, no disruption of the internal elastic lamina).
Objective: We sought to assess the frequency of clinical and histologic features of MLA in patients with cPAN.
Behcet's disease: systemic and ocular manifestations.
Biomed Res Int
June 2014
Department of Ophthalmology, Clinical Centre of Belgrade, Pasterova 2, Belgrade 11000, Serbia.
Aim: The aim of this study was to evaluate if patients with Behcet's disease who have ocular involvement have a more severe form of this disease as compared to patients with Behcet's disease alone.
Methods: A total of 99 patients were included in the study. 76 patients were used as part of the examined group, and 23 patients formed a control group.
[Periarteritis nodosa: gastrointestinal and cardiovascular complications. A case report].
J Med Liban
December 2007
Hôpital Saint-Joseph, Dora-Beyrouth, Services Hépatogastroentérologie, Dora-Beyrouth , Liban.
Polyarteritis nodosa (PAN) is a necrotizing systemic vasculitis involving the wall of small and medium sized arteries. The histologic aspect is defined by the presence of fibrinoid necrosis and an infiltrate rich in neutrophil polynuclears in the artery wall and rare granulomas. Clinical manifestations are misleading, and more often the symptoms of the disease are retrospectively related to the PAN.
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