Difference between revisions of "Vasculitides"
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*Giant cell arteritis (AKA ''temporal arteritis''). | *Giant cell arteritis (AKA ''temporal arteritis''). | ||
*Takayasu's arteritis. | *Takayasu's arteritis. | ||
Notes: | |||
*ANCA = anti-neutrophil cytoplasmic antibodies. | |||
==Giant cell arteritis== | ==Giant cell arteritis== | ||
Line 36: | Line 39: | ||
Treatment: | Treatment: | ||
*Treat right away with high dose steroids. | *Treat right away with high dose steroids. | ||
===Micrograph=== | |||
Features: | |||
*Classical: granulomas. | |||
==Takayasu's arteritis== | ==Takayasu's arteritis== | ||
Line 50: | Line 57: | ||
*Granulomas, giant cells. | *Granulomas, giant cells. | ||
*+/-Patchy necrosis of media. | *+/-Patchy necrosis of media. | ||
==Polyarteritis nodosa== | |||
*Abbreviated ''PAN'' | |||
*Involves small and medium sized vessels. | |||
*Often - renal vessels, mesenteric vessels.<ref>Klatt. AOP P.14.</ref> | |||
*Strong association with ''hepatitis B'' (see [[medical liver diseases]]); ~1/3 of patients with PAN have HBV. | |||
Serology: | |||
*ANCA is usually negative. | |||
===Microscopic=== | |||
Features: | |||
*Inflammatory cells (neutrophils, lymphocytes) within the tunica media. | |||
*Necrosis: dead vessel wall - pink anucleate stuff, nuclear debris (black specks of nuclear material). | |||
==Wegener's granulomatosis== | |||
*Nasal cavity. | |||
*Renal. | |||
*Pulmonary hemorrhage | |||
Notes: | |||
*Pulmonary hemorrhage syndromes:<ref>PBoD p.745.</ref> | |||
**Goodpasture. | |||
**Idiopathic pulmonary hemosiderosis. | |||
**Vasculitis-assoc. hemorrhage (hypersensitivity angiitis, Wegener's granulomatosis). | |||
**Systemic lupus erythematosus. | |||
===Microscopic=== | |||
Features: | |||
*Granulomas typically poorly formed.<ref>PBoD p.747.</ref> | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Cardiovascular pathology]] |
Revision as of 02:02, 22 May 2010
This article deals with the vasculitides (singular vasculitis).
Overview
Most common:[1]
- Polyarteritis nodosa (PAN).
- Microscopic polyangiitis.
- Wegener's granulomatosis.
- Predominantly cutaneous vasculitis.
- Giant cell arteritis (GCA).
Grouping by size
Small vessel vasculitides:
- Predominantly cutaneous vasculitis.
- Henoch-Schoenlein purpura.
- Essential cryoglobulinemic vasculitis.
- ANCA-associated:
- Wegener's granulomatosis (c-ANCA > p-ANCA).
- Churg-Strauss syndrome (50% ANCA +ve).
- Microscopic polyangiitis (usually p-ANCA)
Large vessel vasculitides:[2]
- Giant cell arteritis (AKA temporal arteritis).
- Takayasu's arteritis.
Notes:
- ANCA = anti-neutrophil cytoplasmic antibodies.
Giant cell arteritis
- AKA temporal arteritis.
Clinical
Features:
- Classic finding: jaw claudication, in a patient older than 50 years.
- Other findings: headache, vision loss or diplopia, scalp tenderness, polymyalgia, weight loss, chills, fever.
Work-up:
- CRP, ESR, temporal artery biopsy.
Treatment:
- Treat right away with high dose steroids.
Micrograph
Features:
- Classical: granulomas.
Takayasu's arteritis
General:[3]
- Disease of medium/large arteries.
- Classically involves the aortic arch (leading to decreased pulses in the upper limbs).
- Typically in patients <40 yrs old.
- Usually asian.
Microscopic
Features:[4]
- Adventitial mononuclear infiltrate with perivascular cuffing of the vasa vasorum.
- Mononuclear inflammation in media.
- Granulomas, giant cells.
- +/-Patchy necrosis of media.
Polyarteritis nodosa
- Abbreviated PAN
- Involves small and medium sized vessels.
- Often - renal vessels, mesenteric vessels.[5]
- Strong association with hepatitis B (see medical liver diseases); ~1/3 of patients with PAN have HBV.
Serology:
- ANCA is usually negative.
Microscopic
Features:
- Inflammatory cells (neutrophils, lymphocytes) within the tunica media.
- Necrosis: dead vessel wall - pink anucleate stuff, nuclear debris (black specks of nuclear material).
Wegener's granulomatosis
- Nasal cavity.
- Renal.
- Pulmonary hemorrhage
Notes:
- Pulmonary hemorrhage syndromes:[6]
- Goodpasture.
- Idiopathic pulmonary hemosiderosis.
- Vasculitis-assoc. hemorrhage (hypersensitivity angiitis, Wegener's granulomatosis).
- Systemic lupus erythematosus.
Microscopic
Features:
- Granulomas typically poorly formed.[7]