1. Allergic shock, allergic vasculitis

2. Vasculitis, with stomach pains, so Behcet's.

3. Accompanying vasculitis causes nerve damage- No.

4. And do an M.R.A. for vasculitis too.

5. Vasculitis is the inflammation of the body’s Blood vessels

6. Takayasu's Arteritis (TAK) is an uncommon form of vasculitis

7. Wegener’s granulomatosis (WG), microscopic polyangiitis, and Churg-Strauss syndrome belong to the group of ANCA-associated vasculitides.

8. IgA vasculitis or cutaneous leukocytoclastic vasculitis), hemorrhagic papules and necrotic plaques which occur in acral areas after cooling indicate cryoglobulinemic vasculitis, hemorrhagic papules and macules which develop in patients who start to feel worse and develop fever should arouse suspicion of septic vasulitis, while the simultaneous presence of ulcerating nodules and hemorrhagic papules without predilection for the lower legs will suggest ANCA-associated vasculitis.

9. Temporal Arteritis is a form of vasculitis (inflammation of the blood vessels)

10. Giant cell Arteritis (GCA) is the most common form of vasculitis in adults

11. The serious complications include pericarditis, pulmonary and cutaneous nodules, episcleritis, and rheumatoid vasculitis.

12. The cutaneous vasculitis in this patient presented as a true pustular Bacterid.

13. There is no point in giving a new liver to somebody who also has vasculitis.

14. Thereis now considerable evidence, Chieflyfrom pathological studies, that retroperitoneal fibrosis begins as a vasculitis

15. Temporal Arteritis, now known as giant cell Arteritis, is a form of vasculitis, or blood vessel inflammation

16. In particular, the presence of urine acanthocytes and cellular casts are diagnostic for glomerulonephritis or vasculitis.

17. Vasculitis refers to a group of diseases in which inflammation of the Blood vessels is the hallmark feature

18. 59 rows  · Giant cell Arteritis (GCA) is a form of vasculitis, a group of disorders that …

19. Spontaneous achilles tendon rupture due to a granuloma in patients with vasculitis seems to be a rare event.

20. Among these Coexistences, this review concentrates on vasculitic disorders, with the aim of increasing the awareness of FMF-vasculitis association

21. Temporal Arteritis is a relatively uncommon disorder, but it is the most frequent cause of vasculitis (an inflammation of the blood vessels)

22. Cutaneous necrotizing vasculitis is a not uncommon disorder characterized by an inflammation of the blood vessel walls and skin lesions

23. Bibliography combine upgaze vasculitis consimilar hypoglycaemia clashed double-banked chemicobiological despitefully Sirups Alcotate katana unstanch appliance proctor floods ampere dextrous

24. Angiography demonstrates small vessels well and is the best imaging method available for outlining the beading of vessels seen with vasculitis.

25. Besides the typical lupus forms, nonspecific skin lesions are also observed such as dermal mucinosis, acneiform skin lesions, different variants of livedo, necrotizing vasculitis with ulcers, purpura, urticaria vasculitis, neutrophilic dermatosis, hyperpigmentation, hair and nail changes as well as overlap syndromes with erythema multiforme, scleroderma, Sjögren syndrome, Raynaud phenomenon, lichen planus, bullous pemphigoid und psoriasis.

26. Schönlein described purpura rheumatica (Schönlein's disease) an allergic non-thrombopenic purpura rash that became known as Henoch–Schönlein purpura, though now known as IgA vasculitis.

27. Giant cell Arteritis, also known as temporal Arteritis or cranial Arteritis, is a vasculitis of the large and medium arteries of the head and neck

28. Histomorphologically, small vessel vasculitis with neutrophil alveolitis and diffuse alveolar hemorrhage, as well as extravascular intraparenchymal or peribronchial granulomas, can point to PSV.

29. "Giant cell Arteritis (GCA) is a chronic, idiopathic, granulomatous vasculitis of medium and large arteries comprising overlapping phenotypes of cranial Arteritis and extracranial GCA

30. In addition, the walls of the blood vessels themselves become inflamed (cerebral vasculitis), which leads to decreased blood flow and a third type of edema, "cytotoxic" edema.

31. Atrophie Blanche Synonyms: Atrophie alba, Atrophie blanche en plaque, Atrophie blanche of Milian, Hyalinizing segmental vasculitis, Livedoid vasculopathy, Livedoid vasculitis, Livedo reticularis with summer ulceration, PURPLE (Painful purpuric ulcers with reticular patterning on the lower extremities) ICD-9-CM code: 701.3 Are You Confident of the Diagnosis? What you should be alert for in the

32. Temporal Arteritis (TA), also called giant cell Arteritis (GCA) or cranial Arteritis, is a systemic inflammatory vasculitis of medium and large-sized arteries occurring most frequently in adults

33. Vasculitis can affect very small Blood vessels (capillaries), medium-size Blood vessels, or large Blood vessels such as the aorta (the main blood vessel that leaves the heart)

34. Corticosteroids Commonly referred to as steroids, Corticosteroids are a type of anti-inflammatory drug. They are typically used to treat rheumatologic diseases, like rheumatoid arthritis, lupus or vasculitis (inflammation of the blood vessels)

35. Amarthritis amnionitis amniotitis same as amnionitis ampullitis amygdalitis also called tonsillitis anconitis angiitis same as vasculitis angiocarditis angiocholecystitis (Rare) angiocholitis same as cholangitis angiodermatitis angioleucitis or angioleukitis annexitis same as adnexitis

36. Arrythmical cardiac disease, but it is also associated with coagulation disorders, vasculitis, trauma and conditions of blood vessel dysfunction, such as Marfan syndrome, Ehlers-Danlos syndrome and, as presented in this case, FMD [6-8]

37. Basically three different morphological types can be differentiated: Early after transplantation, diffuse intimal thickening or vasculitis predominate; late after transplantation, focal artheriosclerotic plaques are found; and in some patients a type of dilative angiopathy occurs.

38. Patients with abnormal hepatic Biochemistries had higher frequency of autoimmune hypotiroidism, arthritis, vasculitis, Raynaud's phenomenon, higher sedimentation rate,and higher frequency of antinuclear and antimitochondrial antibodies than patients with normal liver Biochemistries …

39. Atrophie blanche: ( a-trō'fē blahnsh' ), Small smooth ivory-white areas on the skin with hyperpigmented borders and telangiectasis, developing into atrophic stellate scars; seen especially on the legs and ankles of middle-aged women, and associated with livedo reticularis and dermal hyalinizing vasculitis

40. Cv: Challenge Valley (activity, Camp Yawgoog, BSA) Cv: Container Vacuum: Cv: Cryoglobulinemia Vasculitis: Cv: Carrier Volplane (Fixed Wing) Cv: Carrier, General Purpose (US Navy) Cv: Clandestine Vulnerability: Cv: Cache Verification: Cv: Chariot Ventures, LLC (Hong Kong) Cv: Control Vertices Curve (form of NURBS) Cv: Cras Ves'pere (tomorrow

41. Autoimmune Disease-Anti-Neutrophil Cytoplasmic Autoantibody (ANCA) Vasculitis is an autoimmune disease that results in vascular tissue inflammation and systemic vasculitis.Antibodies-Autoimmune response by the body is triggered by autoantibodies.Antibodies react against the antigen present in the wall of neutrophils granulocytes and blood vessels

42. Renal infarction in the general population commonly results from thromboembolism due to structural or Arrythmical cardiac disease, but it is also associated with coagulation disorders, vasculitis, trauma and conditions of blood vessel dysfunction, such as Marfan syndrome, Ehlers-Danlos syndrome and, as presented in this case, FMD [6-8

43. Takayasu’s Arteritis, a rare form of vasculitis, is a chronic condition characterized by inflammation of the largest blood vessel in the body, the aorta, and its branches.The inflammation can result in weakening that leads to aneurysms, ballooning of portions of the vessels that can lead to fatal rupture.

44. Pustular Bacterid.3,4 Typically, patients with palmoplantar pustulosis do not have systemic symptoms such as high fever, and their lesions do not have the histopathological features of leucocytoclastic vasculitis.3,4 Additionally, the typical pustule in palmoplantar pustulosis is located on the palm or sole (plantar arch), not the lateral edge.

45. In this article the diagnostics, differential diagnosis, laboratory findings, multimodal imaging and treatment of vasculitis of small, medium and large vessels as well as granulomatous and eosinophilic vascular diseases are described in the context of previous and current European League against Rheumatism (EULAR) and American College of Rheumatology (ACR) recommendations.

46. Atrophie blanche, also known as Milian's white atrophy, livedoid vasculopathy, livedo reticularis with summer uclerations, segmental hyalinizing vasculitis, or painful purpuric ulcers with reticular pattern of the lower extremities (PPURPLE), is not a specific term but a morphological description, and is a chronic recurrent segmental hyalinizing vascular disease of dermal small blood vessels

47. Clinical manifestations may include one or more of the following: fever, rash or severe dermatologic reactions (e.g., toxic epidermal necrolysis, Stevens-Johnson syndrome); vasculitis, arthralgia, myalgia, serum sickness; allergic pneumonitis, interstitial nephritis; acute renal insufficiency or failure; hepatitis, jaundice, acute hepatic necrosis or failure; anemia, including hemolytic and aplastic; thrombocytopenia, including thrombotic thrombocytopenic purpura; leukopenia; agranulocytosis; pancytopenia; and/or other hematologic abnormalities.