Примери за използване на Systemic vasculitis на Английски и техните преводи на Български
{-}
-
Medicine
-
Colloquial
-
Official
-
Ecclesiastic
-
Ecclesiastic
-
Computer
Systemic vasculitis can be an independent disease.
In patients who have systemic vasculitis, there are similar symptoms.
The vascular cause of inflammation of appendicitis is in systemic vasculitis.
Systemic vasculitis can cause lesions and inflammations throughout the body.
When it comes to the diagnosis of“systemic vasculitis,” what it is, you definitely need to study.
A systemic vasculitis of unknown origin that occurs primarily in children under 8 years of age.
As in previous cases, the following factors can be distinguished in the development of systemic vasculitis.
Systemic vasculitis is a severe inflammatory disease of all vessels, organs and tissues.
Behçet's syndrome(BS), or Behçet's disease,is a systemic vasculitis(inflammation of blood vessels) of unknown cause.
Henoch-Schönlein purpura(systemic vasculitis which affects microvascular arterioles, capillaries and post-capillary venules, often clinically manifested hemorrhagic skin rash combined with joint disease, gastrointestinal tract and kidneys);
HSP, although not a frequent illness of childhood,is the most common systemic vasculitis in children aged between 5 and 15 years.
Examples include acquired conditions such as systemic vasculitis(e.g. ANCA vasculitis) and autoimmune diseases(e.g., lupus), as well as congenital or genetic conditions such as polycystic kidney disease.
Indications for use are connective tissue diseases,including rheumatoid arthritis, systemic vasculitis, polymyositis, dermatomyositis and lupus erythematosus.
Kawasaki disease(KD) is an acute systemic vasculitis, meaning that there is inflammation of the wall of blood vessels that can evolve to dilatations(aneurysms) of any medium-sized artery in the body, primarily the coronary arteries.
GPA(previously called Wegener's granulomatosis) is a chronic systemic vasculitis affecting mainly the small blood vessels and tissues in the upper airways(nose and sinuses), lower airways(lungs) and kidneys.
Secondary glomerular lesions for autoimmune diseases,immune vasculitis, systemic amyloidosis, etc.
In rare cases, patients on therapy with anti-asthma agents, including omalizumab,may present or develop systemic eosinophilia and vasculitis.
Vogt-Koyanagi-Harada syndrome, systemic lupus erythematosus, vasculitis, acute hypersensitivity reactions including urticaria, angioedema, bronchoconstriction, anaphylaxis.
Sarcoidosis, exacerbation of sarcoidosis Systemic lupus erythematosus, vasculitis, rheumatoid arthritis(new or aggravated), Vogt-Koyanagi-Harada no.
Rheumatoid arthritis(new or aggravated) Vogt-Koyanagi-Harada syndrome, systemic lupus erythematosus, vasculitis, acute hypersensitivity reactions including urticaria, angioedema, bronchoconstriction.
Sarcoidosis, exacerbation of sarcoidosis Systemic lupus erythematosus, vasculitis, rheumatoid arthritis(new or aggravated), Vogt-Koyanagi-Harada syndrome, acute hypersensitivity reactions including no.
Exacerbation of sarcoidosis Systemic lupus erythematosus, vasculitis, rheumatoid arthritis(new or aggravated), Vogt-Koyanagi-Harada syndrome, acute hypersensitivity reactions including urticaria, angioedema, bronchoconstriction, anaphylaxis§.
Other less common causes of ulcers,include systemic diseases such as systemic sclerosis, vasculitis and various skin conditions especially pyoderma gangrenosum.
Sometimes JDM can look like other autoimmune disease(such as arthritis, Systemic Lupus Erythematosus, or vasculitis) or like a congenital muscle disease.
Leukocytoclastic vasculitis, Drug Reaction with Eosinophilia and Systemic Symptoms^.
There are also many less common causes of ulcers including systemic diseases such as systemic sclerosis, vasculitis and various skin conditions especially pyoderma gangrenosum.
This includes Rheumatoid Arthritis and off-label autoimmune diseases,including Systemic Lupus Erythematosus(SLE) and Vasculitis.
Allergic reactions(bronchospasm, hypersensitivity, urticaria), autoantibody positive Rare:Serious systemic hypersensitivity reactions(including anaphylactic reaction), vasculitis(systemic), sarcoidosis.
Systemic pathology, called Henoch purpura disease or hemorrhoidal vasculitis, mostly affects children.
Churg-Strauss syndrome and hypereosinophilic syndrome Patients with severe asthma may rarely present systemic hypereosinophilic syndrome or allergic eosinophilic granulomatous vasculitis(Churg-Strauss syndrome), both of which are usually treated with systemic corticosteroids.