Zagazig University Digital Repository
Home
Thesis & Publications
All Contents
Publications
Thesis
Graduation Projects
Research Area
Research Area Reports
Search by Research Area
Universities Thesis
ACADEMIC Links
ACADEMIC RESEARCH
Zagazig University Authors
Africa Research Statistics
Google Scholar
Research Gate
Researcher ID
CrossRef
laboratory assessment of autoimmune vasculitis
Faculty
Medicine
Year:
2009
Type of Publication:
Theses
Pages:
153
Authors:
Rania Mustafa Ibrahim
BibID
10901896
Keywords :
Pathology
Abstract:
Kawasaki disease (KD) is an acute systemic vasculitis of unknown etiology that predominantly affects infants and young children. It is considered the most common cause of acquired heart disease in children in the United States. Diagnosis is based on clinical criteria. However, these criteria have low sensitivity and specificity and therefore, otherlaboratory features may be helpful in establishing the diagnosis.Wegener’s granulomatosis is a rare complex multisystem disease. Early diagnosis is essential to prevent potentially life threatening renal and pulmonary injury. The antineutrophil cytoplasmic antibody test (cANCA) are the most reliable diagnostic procedures for WG.MPA is more frequent than WG in Southern Europe and Japan. In fact, it is the most common vasculitic cause for the pulmonary-renal syndrome.Churg-Strauss syndrome is a rare diffuse vasculitis that is almost invariably accompanied by severe asthma. The cause of Churg-Strauss syndrome is unknown, but its characteristic histological findings and association with asthma distinguish it from other vasculitides. A clear diagnosis of Churg-Strauss syndrome might not be made until the abdominal viscera, heart, or nervous system become involved, which may be fatal in the latter two systems. The association of Churg-Strauss syndrome with antineutrophil cytoplasmic antibodies has facilitated diagnosis of this disease.Henoch-Schonlein purpura is the most common systemic vasculitis in children. Boys are affected more often than girls. About half of the cases of HSP are preceded by an upper respiratory infection. It has been suggested that group A beta-hemolytic streptococcus may be a trigger factorCryoglobulinemic vasculitis is considered to be a relatively rare disorder. The leading cause of death in MC is liver impairment, followed by cardiovascular disorders and renal insufficiency.Hypersensitivity vasculitis occurs equally in both sexes and at all ages. It is usually easily diagnosed by clinical and histologic features.
PDF
جامعة المنصورة
جامعة الاسكندرية
جامعة القاهرة
جامعة سوهاج
جامعة الفيوم
جامعة بنها
جامعة دمياط
جامعة بورسعيد
جامعة حلوان
جامعة السويس
شراقوة
جامعة المنيا
جامعة دمنهور
جامعة المنوفية
جامعة أسوان
جامعة جنوب الوادى
جامعة قناة السويس
جامعة عين شمس
جامعة أسيوط
جامعة كفر الشيخ
جامعة السادات
جامعة طنطا
جامعة بنى سويف