Vasculitis pathophysiology: Difference between revisions

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===Small vessel vasculitis===
===Small vessel vasculitis===
* [[Churg-Strauss syndrome|Churg-Strauss arteritis]] - Affects medium and small vessels with vascular and extravascular granulomatosis. Classically involves arteries of lungs and skin, but may be generalized.  
* [[Churg-Strauss syndrome|Churg-Strauss arteritis]] - affects medium and small vessels with vascular and extravascular granulomatosis. Classically involves arteries of lungs and skin, but may be generalized.  
* [[microscopic polyangiitis|Microscopic polyarteritis/polyangiitis]] - Affects [[capillaries]], [[venules]], or [[arterioles]]. Thought to be part of a group that includes [[Wegeners]] since both are associated with [[ANCA]] and similar extrapulmonary manifestations. Patients do not usually have symptomatic or histologic respiratory involvement.
* [[microscopic polyangiitis|Microscopic polyarteritis/polyangiitis]] - affects [[capillaries]], [[venules]], or [[arterioles]]. Thought to be part of a group that includes [[Wegeners]] since both are associated with [[ANCA]] and similar extrapulmonary manifestations. Patients do not usually have symptomatic or histologic respiratory involvement.
* [[Hypersensitivity vasculitis]] - Usually due to a [[hypersensitivity]] reaction to a known drug. There is presence of skin vaculitis with palpable [[petechiae]] or [[purpura]]. Biopsy of these lesions reveal inflammation of the small vessels, termed leukocytoclastic vasculitis, which is most prominent in postcapillary venules.
* [[Hypersensitivity vasculitis]] - usually due to a [[hypersensitivity]] reaction to a known drug. There is presence of skin vaculitis with palpable [[petechiae]] or [[purpura]]. Biopsy of these lesions reveal inflammation of the small vessels, termed leukocytoclastic vasculitis, which is most prominent in postcapillary venules.
* [[Henoch-Schonlein purpura]] - Systemic vasculitis due to tissue deposition of [[IgA]]-containing immune complexes. Biopsy of lesions shows inflammation of small vessels. It is considered a form of hypersensitivity vasculitis but is distinguished by prominent deposits of IgA. This is the most common vasculitis in children.
* [[Henoch-Schonlein purpura]] - systemic vasculitis due to tissue deposition of [[IgA]]-containing immune complexes. Biopsy of lesions shows inflammation of small vessels. It is considered a form of hypersensitivity vasculitis but is distinguished by prominent deposits of IgA. This is the most common vasculitis in children.
* [[Essential cryoglobulinemic vasculitis]] - Most often due to [[hepatitis C infection]], immune complexes of [[cryoglobulins]] --- proteins that consists of [[immunoglobulins]] and [[complement]] and precipitate in the cold while dissolving upon rewarming --- are deposited in walls of capillaries, venules, or arterioles.
* [[Essential cryoglobulinemic vasculitis]] - most often due to [[hepatitis C infection]], immune complexes of [[cryoglobulins]] --- proteins that consists of [[immunoglobulins]] and [[complement]] and precipitate in the cold while dissolving upon rewarming --- are deposited in walls of capillaries, venules, or arterioles.
* Vasculitis secondary to connective tissue disorders - Usually secondary to [[lupus erythematosus| systemic lupus erythematosus]] (SLE), [[rheumatoid arthritis]] (RA), relapsing [[polychondritis]], [[Behcet's disease]], and other connective tissue disorders.
* Vasculitis secondary to connective tissue disorders - usually secondary to [[lupus erythematosus| systemic lupus erythematosus]] (SLE), [[rheumatoid arthritis]] (RA), relapsing [[polychondritis]], [[Behcet's disease]], and other connective tissue disorders.
* Vasculitis secondary to viral infection
* Vasculitis secondary to viral infection



Revision as of 12:25, 31 August 2012

Vasculitis

Overview

Classification

Large-sized vessel vasculitis
Takayasu's Arteritis
Temporal Arteritis
Medium-sized vessel vasculitis
Kawasaki's Disease
Polyarteritis Nodosa
Small-sized vessel vasculitis
Churg-Strauss Syndrome
Cutaneous leukocytoclastic vasculitis
Essential cryoglobulinemic vasculitis
Henoch-Schonlein Purpura
Microscopic polyangiitis
Wegener's Granulomatosis
Variable-sized vessel vasculitis
Sjogren syndrome
Cogan syndrome
Single organ vasculitis
Primary central nervous system angiitis

Causes

Differential Diagnosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: M.Umer Tariq [2]

Overview

Pathophysiology

Large vessel vasculitis

Medium vessel vasculitis

  • Polyarteritis nodosa - Systemic necrotizing vasculitis and aneurysm formation affecting both medium and small arteries. If only small vessels are affected, it is called microscopic polyangiitis, although it is more associated with Wegener's granulomatosis than to classic PAN.
  • Wegener's granulomatosis - Systemic vasculitis of medium and small arteries, including venules and arterioles. Produces granulomatous inflammation of the respiratory tracts and necrotizing, pauci-immune glomerulonephritis. Most common cause of saddle nose deformity in USA (nose flattened due to destruction of nasal septum by granulomatous inflammation).
  • Kawasaki disease - Usually in children, it affects large, medium, and small vessels, prominently the coronary arteries. Associated with a mucocutaneous lymph node syndrome.
  • Isolated CNS vasculitis - Affects medium and small arteries over a diffuse CNS area, without symptomatic extracranial vessel involvement.

Small vessel vasculitis

Gross Pathology

Kidney: Petechiae: Gross natural color, an excellent example of flea bitten kidney case had necrotizing vasculitis
Skin:Leucocytolastic vasculitis; a close up view


Microscopic Pathology

Kidney: Transplant: Micro H&E high mag excellent example acute vasculitis due to rejection
Coronary artery: Transplant Rejection: Micro high mag H&E small muscular artery vasculitis
Vasculitis, Rocky Mountain Spotted Fever, immunoperoxidase staining vessels for Rickettsia rickettsii


References

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