Difference between revisions of "Vasculitides"

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[[Image:Churg-Strauss syndrome - high mag.jpg|thumb|right|[[Micrograph]] showing a vasculitis. [[H&E stain]].]]
This article deals with the '''vasculitides''' (singular ''vasculitis'').  Vascular disease that is not vasculitides is covered in the article ''[[vascular disease]]''.   
This article deals with the '''vasculitides''' (singular ''vasculitis'').  Vascular disease that is not vasculitides is covered in the article ''[[vascular disease]]''.   


Revision as of 05:45, 10 December 2014

Micrograph showing a vasculitis. H&E stain.

This article deals with the vasculitides (singular vasculitis). Vascular disease that is not vasculitides is covered in the article vascular disease.

The histology of normal vessels is dealt with in normal blood vessels.

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

Definition

Small vessel vasculitis = vasculitis of vessels smaller than arteries; affects arterioles, venules, and capillaries.[2]

  • What is an arteriole?
    • There is no histologic definition according to Sternberg's Histology for Pathologists; however, a diameter of <100 micrometers is suggested as a definition.[3]
Types

Notes:

  • ANCA = anti-neutrophil cytoplasmic antibodies.
    • The terminology has changed as more knowledge has been gained:
      • MPO-ANCA = p-ANCA.
      • PR3-ANCA = c-ANCA.

Medium vessel vasculitides[4]

Large vessel vasculitides[4]

Grouping by hypersensitivity

Cell-mediated hypersensitivity:[5]

  • Giant cell arteritis.
  • Takayasu arteritis.
  • Churg-Strauss disease.
  • Wegener’s granulomatosis.

Note:

  • All have granulomas.

Immune complex mediated hypersensitivity:[5]

Pathologist's role in the diagnosis of vasculitis

General

  • Pathologists often cannot, based on morphology alone, arrive at the definitive diagnosis.
  • The presentation & distribution are more characteristic than the pathology.[6][7]

Microscopic

Features - both #1 and #2 are required:[8]

  1. Inflammatory cells within the blood vessel wall.
  2. Vessel injury:
    • Frank fibrinoid necrosis or nuclear dust:
      • Fibrinoid necrosis = anucleate amorphous intensely eosinophilic material.
        • Amorphous = no definite form.[9]
      • "Nuclear dust" = punctate hyperchromatic material ~ 1 micrometre.

Notes:

  • Involvement is usually patchy.
    • If there is an inkling of vasculitis... it should prompt deeper cuts.

Features to consider

  1. Presence of granulomas.
  2. Type inflammatory cells, i.e. eosinophils, mononuclear cells.
  3. Size of vessels involved.
  4. Extent of involvement.
  5. Acuity (acute vs. subacute vs. chronic vs. acute on chronic).
    • Chronic = thick fibrotic appearing vessels with a small lumen.

Vasculitis versus neuropathy

Domain Vasculitis Neuropathy
Clinical pain, diffuse/
patchy distribution 		focal/isolated
Pathological
(inflammatory cells) 		epineurium endoneurium

Small vessel vasculitides

The follow section has information specific to the individual types of small vessel vasculitis.

Small vessel leukocytoclastic vasculitis

  • AKA leukocytoclastic vasculitis, abbreviated LCV.

General

  • Most common cutaneous vasculitis.[10]

Clinical:

  • Palpable purpura, usu. lower extremity.

Microscopic

Features:[10]

  • Small upper dermis vessels with:
    1. Neutrophils.
      • Fragmentation of neutrophils (leukocytoclasia).
    2. Vessel damage: fibrin deposition (bright pink acellular stuff).

Has a very broad DDx:[10]

  1. Infectious:
  2. Vasculitic disorders:
  3. Other:

Image:

Stains

  • PAS - look for fungus.

Microscopic polyangiitis

General

  • Classically MPO-ANCA (p-ANCA) +ve.

Microscopic

Features - small-sized vessels with:

  • Inflammatory cells (neutrophils, lymphocytes) within the tunica media.
  • Fibroid necrosis: dead vessel wall - pink anucleate stuff, nuclear debris (black specks of nuclear material).
  • No granulomas.

Images:

Wegener granulomatosis

  • Abbreviated WG.
  • AKA granulomatosis with polyangiitis.

General

  • Autoimmune.

Clinical

Serology:

Notes:

Microscopic

Features:

  • Small vessel vasculitis:
    1. Inflammatory cells within the vessel wall.
      • Granulomas - typically poorly formed.[14]
        • Multinucleated giant cells - common. (???)
    2. Vessel wall injury.

Notes:

  • In the lung, the granulomas tend to be centrilobular, as the artery travels with the airway and is centrilobular.
    • It may difficult to find small blood vessels in affected portions of lung.

Images

  • WG - intermed. mag. (WC)

  • WG - very high mag. (WC)

  • WG - intermed. mag. (WC)

  • WG - high mag. (WC)

  • WG - very high mag. (WC)

www:

Churg-Strauss syndrome

  • Abbreviated CSS.
  • AKA allergic granulomatous angiitis.[15]
  • AKA Churg-Strauss disease.

General

Defining features - memory device GAFE:

  • Granulomata.
  • Asthma.
  • Fever.
  • Eosinophilia.

Notes:

Microscopic

Features:

DDx:

Images

  • CSS - high mag. (WC)

  • CSS - very high mag. (WC)

Medium vessel vasculitides

The follow section has information specific to the individual types of medium vessel vasculitis.

Kawasaki disease

General

  • Medium vessel disease.
  • Classically afflicts the coronary arteries of children - usu. less than 5 years old.
    • May lead to coronary artery aneurysms.[18]

Clinical features - mnemonic Warm CREAM:[19]

  • Warm = fever.
  • Conjunctivitis, non-exudative.
  • Rash, polymorphous.
  • Erythema or edema of hands and feet.
  • Adenopathy, usu. cervical and unilateral.
  • Mucosal manifestations - strawberry tongue, cracked lips.

Treatment:

  • High dose IV aspirin.

Microscopic

Features:

  • Medium-sized vessels with intramural inflammatory cells.
  • Vessel destruction, e.g. fibrinoid necrosis (very pink anucleate arterial wall).

Polyarteritis nodosa

  • Abbreviated PAN.

General

  • Involves small and medium sized vessels.
  • Often - renal vessels, mesenteric vessels.[20]
    • Classically, lung involvement by PAN is considered to be rare, though this may not be entirely true.[21]
  • Strong association with hepatitis B (see medical liver diseases); ~1/3 of patients with PAN have HBV.

Serology:

  • ANCA is usually negative.

Microscopic

Features - medium-sized vessels with:

  • Inflammatory cells (neutrophils, lymphocytes) within the tunica media.
  • Fibroid necrosis: dead vessel wall - pink anucleate stuff, nuclear debris (black specks of nuclear material).
    • Usu. focal (wall) involvement; classically leads to berry microaneurysms - ergo the name polyarteritis nodosa.

Image:

Large vessel vasculitides

The follow section has information specific to the individual types of large vessel vasculitis.

Giant cell arteritis

Temporal artery redirects here.
  • Abbreviated GCA.
  • AKA temporal arteritis.

General

  • Classically afflicts the temporal artery.

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.
    • ESR normal (>50 years old): <20 mm/hr males, <30 mm/hr females.[22]

Treatment:

  • Treat right away with high dose steroids.
    • Biopsy is confirmatory.

Microscopic

Features:

  • Artery with intramural inflammatory cells.
  • Destruction of arterial wall, e.g. fibrinoid necrosis (pink anucleate arterial wall).

Image(s):

Sign out

Negative

TEMPORAL ARTERY, LEFT, BIOPSY:
- MEDIUM SIZE ARTERY WITHOUT PATHOLOGIC DIAGNOSIS, SEE COMMENT.

COMMENT:
A negative biopsy does not rule out the possibility of giant cell (temporal) 
arteritis, as this may be a focal disorder. The clinical management is 
dependent upon the clinical impression.

Takayasu arteritis

General

Features:[23]

  • 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.

Pathogenesis:

Gross

Features:[23]

  • Classically involves the aortic arch.

Microscopic

Features:[23]

  • Adventitial mononuclear infiltrate with perivascular cuffing of the vasa vasorum.
  • Mononuclear inflammation in media.
  • Granulomas, giant cells.
  • +/-Patchy necrosis of media.

Other

Aortitis

General

  • Uncommon.

Gross

Features:

  • Tree bark-like appearance.

Notes:

  • Several blocks should be submitted.

Image:

Microscopic

Features:

  • Inflammatory cells.

Subclassification:

  • Granulomatous.
  • Lymphoplasmacytic pattern.
  • Mixed inflammatory.
  • Suppurative.

LAMP-2 vasculitis

  • Associated with pauci-immune necrotizing and crescentic glomerulonephritis.[27]
  • Grouped with the ANCA-associated vasculitides.[28]

See also

References

  1. ↑ Yeung, J.C.; Leonard, Blair J. N. (2005). The Toronto Notes 2005 - Review for the MCCQE and Comprehensive Medical Reference (2005 ed.). The Toronto Notes Inc. for Medical Students Inc.. pp. RH3. ISBN 978-0968592854.
  2. ↑ Jennette JC, Falk RJ (November 1997). "Small-vessel vasculitis". N. Engl. J. Med. 337 (21): 1512–23. doi:10.1056/NEJM199711203372106. PMID 9366584. http://www.nejm.org/doi/full/10.1056/NEJM199711203372106.
  3. ↑ Sternberg, Stephen S. (1997). Histology for Pathologists (2nd ed.). Lippincott Williams & Wilkins. pp. 769. ISBN 978-0397517183.
  4. ↑ 4.0 4.1 Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 512. ISBN 978-1416031215.
  5. ↑ 5.0 5.1 URL: http://dermind.tripod.com/vasculitis.htm. Accessed on: 30 April 2012.
  6. ↑ URL: http://www.pathology.ubc.ca/path425/PrincipleofPathophysiology/CirculatoryDisorders/SystemicVasculitisDrBWalker.doc. Accessed on: 26 November 2010.
  7. ↑ URL: http://www.icapture.ubc.ca/who/who_bios_david_walker.shtml. Accessed on: 26 November 2010.
  8. ↑ Dillon, MJ.; Eleftheriou, D.; Brogan, PA. (Sep 2010). "Medium-size-vessel vasculitis.". Pediatr Nephrol 25 (9): 1641-52. doi:10.1007/s00467-009-1336-1. PMC 2908435. PMID 19946711. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908435/.
  9. ↑ URL: http://dictionary.weather.net/dictionary/amorphous. Accessed on: 26 November 2010.
  10. ↑ 10.0 10.1 10.2 Brinster, NK. (Nov 2008). "Dermatopathology for the surgical pathologist: a pattern-based approach to the diagnosis of inflammatory skin disorders (part II).". Adv Anat Pathol 15 (6): 350-69. doi:10.1097/PAP.0b013e31818b1ac6. PMID 18948765.
  11. ↑ Kraft, DM.; Mckee, D.; Scott, C. (Aug 1998). "Henoch-Schönlein purpura: a review.". Am Fam Physician 58 (2): 405-8, 411. PMID 9713395.
  12. ↑ Yeung, J.C.; Leonard, Blair J. N. (2005). The Toronto Notes 2005 - Review for the MCCQE and Comprehensive Medical Reference (2005 ed.). The Toronto Notes Inc. for Medical Students Inc.. pp. RH6. ISBN 978-0968592854.
  13. ↑ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 745. ISBN 0-7216-0187-1.
  14. ↑ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 747. ISBN 0-7216-0187-1.
  15. ↑ http://emedicine.medscape.com/article/333492-overview
  16. ↑ URL: http://emedicine.medscape.com/article/334024-overview. Accessed on: 22 January 2011.
  17. ↑ Chen, KR.; Su, WP.; Pittelkow, MR.; Conn, DL.; George, T.; Leiferman, KM. (Aug 1996). "Eosinophilic vasculitis in connective tissue disease.". J Am Acad Dermatol 35 (2 Pt 1): 173-82. PMID 8708015.
  18. ↑ Taubert, KA.; Shulman, ST. (Jun 1999). "Kawasaki disease.". Am Fam Physician 59 (11): 3093-102, 3107-8. PMID 10392592.
  19. ↑ URL: http://www.medicalmnemonics.com/cgi-bin/return_browse.cfm?&system=Other%2FMiscellaneous&discipline=Pathology&browse=1. Accessed on: 14 January 2012.
  20. ↑ Klatt, Edward C. (2006). Robbins and Cotran Atlas of Pathology (1st ed.). Saunders. pp. 14. ISBN 978-1416002741.
  21. ↑ Matsumoto, T.; Homma, S.; Okada, M.; Kuwabara, N.; Kira, S.; Hoshi, T.; Uekusa, T.; Saiki, S. (Jul 1993). "The lung in polyarteritis nodosa: a pathologic study of 10 cases.". Hum Pathol 24 (7): 717-24. PMID 8100552.
  22. ↑ URL: http://www.nlm.nih.gov/medlineplus/ency/article/003638.htm. Accessed on: 17 August 2012.
  23. ↑ 23.0 23.1 23.2 Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 538. ISBN 0-7216-0187-1.
  24. ↑ Arnaud, L.; Haroche, J.; Mathian, A.; Gorochov, G.; Amoura, Z. (Nov 2011). "Pathogenesis of Takayasu's arteritis: a 2011 update.". Autoimmun Rev 11 (1): 61-7. doi:10.1016/j.autrev.2011.08.001. PMID 21855656.
  25. ↑ URL: http://dermind.tripod.com/vasculitis.htm. Accessed on: 30 April 2012.
  26. ↑ Vaideeswar, P.. "Syphilitic aortitis: rearing of the ugly head.". Indian J Pathol Microbiol 53 (4): 624-7. doi:10.4103/0377-4929.72002. PMID 21045381.
  27. ↑ Bosch X, Mirapeix E (May 2009). "Vasculitis syndromes: LAMP-2 illuminates pathogenesis of ANCA glomerulonephritis". Nat Rev Nephrol 5 (5): 247–9. doi:10.1038/nrneph.2009.51. PMID 19384321. http://www.nature.com/ki/journal/v76/n1/abs/ki2009123a.html.
  28. ↑ Chen M, Kallenberg CG (2009). "New advances in the pathogenesis of ANCA-associated vasculitides". Clin. Exp. Rheumatol. 27 (1 Suppl 52): S108–14. PMID 19646356.
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