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==
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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==
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*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]

References

  1. TN05 RH3.
  2. TN05 RH20.
  3. PBoD P.538.
  4. PBoD P.538.
  5. Klatt. AOP P.14.
  6. PBoD p.745.
  7. PBoD p.747.