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Vasculitis

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Vasculitis
SpecialtyImmunology, angiology, rheumatology Edit this on Wikidata

Vasculitis (plural: vasculitides)[1] refers to a heterogeneous group of disorders that are characterized by inflammatory destruction of blood vessels.[2] Both arteries and veins are affected. Lymphangitis is sometimes considered a type of vasculitis.[3] Vasculitis is primarily due to leukocyte migration and resultant damage.

Although both occur in vasculitis, inflammation of veins (phlebitis) or arteries (arteritis) on their own are separate entities.

Classification

There are many ways to classify vasculitis.

  • It can be classified by the underlying cause. For example, the cause of syphilitic aortitis is infectious (aortitis simply refers to arteritis of the aorta, which is an artery.) However, the cause of many forms of vasculitis are poorly understood. There is usually an immune component, but the trigger is often not identified. In these cases, the antibody found is sometimes used in classification, as in ANCA-associated vasculitides.
  • It can be classified by the location of the affected vessels. For example, ICD-10 classifies "vasculitis limited to skin" with skin conditions (under "L"), and "necrotizing vasculopathies" with musculoskeletal system and connective tissue conditions (under "M"). Arteritis/phlebitis on their own are classified with circulatory conditions (under "I").
  • Vasculitides can be classified by the type or size of the blood vessels that they predominantly affect.[4] Apart from the arteritis/phlebitis distinction mentioned above, vasculitis is often classified by the caliber of the vessel affected. However, there can be some variation in the size of the vessels affected.

According to the size of the vessel affected, vasculitis can be classified into: [5]

Large vessel: - Behçet's syndrome - Giant cell arteritis - Polymyalgia rheumatica - Takayasu's arteritis

Medium vessel: - Cutaneous vasculitis - Polyarteritis nodosa - Kawasalki disease - Berger disease

Small vessel: - Churg-Strauss syndrome - Cutaneous vasculitis - Henoch-Schönlein purpura - Microscopic polyangiitis - Wegener's granulomatosis


Conditions

Some disorders have vasculitis as their main feature. The major types are given in the table below:

Comparison of major types of vasculitis[6]
Vasculitis Affected organs Histopathology
Cutaneous small-vessel vasculitis Skin, kidneys Neutrophils, fibrinoid necrosis
Wegener's granulomatosis Nose, lungs, kidneys Neutrophils, giant cells
Churg–Strauss syndrome Lungs, kidneys, heart, skin Histiocytes, eosinophils
Kawasaki disease Skin, heart, mouth, eyes Lymphocytes, endothelial necrosis
Buerger's disease Leg arteries and veins (gangrene) Neutrophils, granulomas

Takayasu's arteritis, polyarteritis nodosa and giant cell arteritis are sometimes classified as vasculitis as well, but rather belong to arteritis since they mainly involve arteries.

Furthermore, there are many conditions that have vasculitis as an accompanying or atypical symptom, including:

Symptoms

Petechia and purpura on the low limb due to medication induced vasculitis.

Possible symptoms include:[7]

Diagnosis

Treatment

Treatments are generally directed toward stopping the inflammation and suppressing the immune system. Typically, cortisone-related medications, such as prednisone, are used. Additionally, other immune suppression drugs, such as cyclophosphamide and others, are considered. In case of an infection, antimicrobial agents including cephalexin may be prescribed. Affected organs (such as the heart or lungs) may require specific medical treatment intended to improve their function during the active phase of the disease.

References

  1. ^ "Vasculitis - Definition from the Merriam-Webster Online Dictionary". Retrieved 2009-01-08.
  2. ^ "Glossary of dermatopathological terms. DermNet NZ". Retrieved 2009-01-08.
  3. ^ "Vasculitis" at Dorland's Medical Dictionary
  4. ^ Jennette JC, Falk RJ, Andrassy K; et al. (1994). "Nomenclature of systemic vasculitides. Proposal of an international consensus conference". Arthritis Rheum. 37 (2): 187–92. doi:10.1002/art.1780370206. PMID 8129773. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  5. ^ http://www.merckmanuals.com/professional/musculoskeletal_and_connective_tissue_disorders/vasculitis/overview_of_vasculitis.html
  6. ^ Unless else specified in boxes, then reference is:
    • Stevens & Lowe: Pathology. At Fleshandbones.com
  7. ^ "The Johns Hopkins Vasculitis Center - Symptoms of Vasculitis". Retrieved 2009-05-07.