Results 61 to 70 of about 27,299 (305)
Cutaneous Polyarteritis Nodosa in Childhood: A Case Report and Review of the Literature [PDF]
Polyarteritis nodosa is a rare vasculitis of childhood. Cutaneous PAN (cPAN) is limited to the skin, muscles, joints, and peripheral nerves. We describe a 7.5-year-old girl with cPAN presenting initially as massive cervical edema who later went on to ...
Bansal, Nina-Karen+1 more
core +3 more sources
Expert Perspectives on a Clinical Challenge: Hematologic Malignancies and Vasculitis
Systemic vasculitis describes a collection of rare diseases each caused by inflammation of blood vessel walls that can cause severe systemic complications [[3, 4]](#ref‐0003). The pattern of vascular inflammation and resultant damage is frequently variable and may be mimicked, or directly triggered, by infection or malignancy.
Michelle L. Robinette, Hetty E. Carraway
wiley +1 more source
Medium-size-vessel vasculitis [PDF]
Medium-size-artery vasculitides do occur in childhood and manifest, in the main, as polyarteritis nodosa (PAN), cutaneous PAN and Kawasaki disease. Of these, PAN is the most serious, with high morbidity and not inconsequential mortality rates.
A Bakkaloglu+179 more
core +2 more sources
Dental Implant Therapy in Patients With Autoimmune Diseases: A Scoping Review
ABSTRACT Objectives The aim of this scoping review is to determine the effects of autoimmune diseases (ADs) and the agents used for treatment on dental implant survival and biologic outcomes. Material and Methods An electronic database search was performed in MEDLINE (PubMed), The Cochrane Library, and Embase on 29‐04‐2024.
Emil Hyldahl+2 more
wiley +1 more source
Demystifying “Hyaline Angiopathy” of Pulse Granuloma in Oral and Extraoral Surgical Pathology
ABSTRACT Background and Objectives Pulse granuloma (PG), or giant cell hyaline angiopathy, is an immune‐mediated reaction often following the implantation of plant‐derived food particles. PGs are primarily found in the oral cavity and gastrointestinal tract and may represent a histopathological pitfall, being mistaken for other granulomatous conditions
Felipe Fornias Sperandio+3 more
wiley +1 more source
ABSTRACT We present a neonate born to a mother with a known diagnosis of cutaneous polyarteritis nodosa (cPAN) who presented with acrocyanosis on the first day of life, which progressed to livedo reticularis and eventual digital necrosis and autoamputation.
Marin P. Melloy, Sheilagh Maguiness
wiley +1 more source
Retrospective study on Encephalitozoon cuniculi infections in 118 cat and 9 dog eyes
Abstract Purpose This study aims to inform about the clinical image, diagnostic possibilities, and treatment options for cats and dogs diagnosed with ocular encephalitozoonosis. Materials and Methods Medical records of 7 dogs and 75 cats with ocular encephalitozoonosis presented at the Clinical Unit of Ophthalmology of the University of Veterinary ...
Sophie Hofmann‐Wellenhof, Barbara Nell
wiley +1 more source
The aim of the study – to determine the diagnostic value of serum levels of endothelin-1, alpha-actin-2 and elastin in patients with primary systemic vasculitis. Materials and methods.
L. B. Petelytska, O. B. Yaremenko
doaj +1 more source
Incidence of Pneumocystis jiroveci Pneumonia among Groups at Risk in HIV-negative Patients
International audienceBackground - Pneumocystis jiroveci pneumonia in human immunodeficiency virus (HIV)-negative immunocompromised patients is associated with high mortality rates.
Decaux, Olivier+10 more
core +3 more sources
A rare case of childhood polyarteritis nodosa successfully treated with etanercept [PDF]
Childhood Polyarteritis Nodosa (CPAN) a rare and often fatal disease tends to be more common in individuals of Asian descent. Previously it was referred to as Infantile PAN.
Kamath, Pragathi+2 more
core +2 more sources