» Articles » PMID: 24072416

Overview of the 2012 Revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides

Overview
Publisher Springer
Specialty Nephrology
Date 2013 Sep 28
PMID 24072416
Citations 138
Authors
Affiliations
Soon will be listed here.
Abstract

The nomenclature and classification of vasculitis has been difficult and controversial for many decades. This is problematic both for research on vasculitis as well as clinical care of patients with vasculitis. The first (1994) International Chapel Hill Consensus Conference on the Nomenclature of Systemic Vasculitides (CHCC) proposed names and definitions for the most common forms of vasculitis. Since then, there have been substantial advances in our understanding of vasculitis and changes in medical terminology. In addition, CHCC 1994 did not propose a nomenclature for some relatively common forms of vasculitis, such as vasculitis secondary to other diseases. To address these issues, a second International Chapel Hill Consensus Conference was held in 2012. The goals were to change names and definitions as appropriate, and add important categories of vasculitis not included in CHCC 1994. This overview summarizes the 2012 CHCC and points out the changes compared to the 1994 CHCC. Notable changes include the introduction of new terms such as granulomatosis with polyangiitis, eosinophilic granulomatosis with polyangiitis and immunoglobulin A vasculitis and the inclusion of categories for variable vessel vasculitis and secondary forms of vasculitis.

Citing Articles

Recurrent Vision Loss in a Patient with Giant Cell Arteritis while on High Dose Corticosteroids.

Barton A, Francis E, Feibelman P, Geary M, Booy D J Brown Hosp Med. 2025; 3(2):92898.

PMID: 40026787 PMC: 11864387. DOI: 10.56305/001c.92898.


The association between serum lipids at diagnosis and renal outcome in microscopic polyangiitis patients.

Zheng Z, Wang Y, Xie J, Chen Z, Jiang B, Xu Y PeerJ. 2025; 13:e18839.

PMID: 39950045 PMC: 11823655. DOI: 10.7717/peerj.18839.


A Machine Learning Model Based on Radiomic Features as a Tool to Identify Active Giant Cell Arteritis on [F]FDG-PET Images During Follow-Up.

Vries H, van Praagh G, Nienhuis P, Alic L, Slart R Diagnostics (Basel). 2025; 15(3).

PMID: 39941297 PMC: 11817507. DOI: 10.3390/diagnostics15030367.


Treatment With Avacopan in Patients With Respiratory Tract Manifestations of Antineutrophil Cytoplasmic Antibody-Associated Vasculitis.

Specks U, Spiera R, Fussner L, Lebovics R, Bray S, Gurlin R ACR Open Rheumatol. 2025; 7(1):e11795.

PMID: 39854178 PMC: 11760992. DOI: 10.1002/acr2.11795.


Granulomatosis With Polyangiitis in an Autistic Patient With Depression: Challenges in Diagnosis and Management.

Javed A, Zhyzhneuskaya S, Khalid N, Rajabally H Cureus. 2024; 16(11):e73037.

PMID: 39640133 PMC: 11619002. DOI: 10.7759/cureus.73037.


References
1.
Falk R, Gross W, Guillevin L, Hoffman G, Jayne D, Jennette J . Granulomatosis with polyangiitis (Wegener's): an alternative name for Wegener's granulomatosis. Ann Rheum Dis. 2011; 70(4):704. DOI: 10.1136/ard.2011.150714. View

2.
Suzuki H, Kiryluk K, Novak J, Moldoveanu Z, Herr A, Renfrow M . The pathophysiology of IgA nephropathy. J Am Soc Nephrol. 2011; 22(10):1795-803. PMC: 3892742. DOI: 10.1681/ASN.2011050464. View

3.
Jennette J, Falk R, Andrassy K, Bacon P, Churg J, Gross W . Nomenclature of systemic vasculitides. Proposal of an international consensus conference. Arthritis Rheum. 1994; 37(2):187-92. DOI: 10.1002/art.1780370206. View

4.
Falk R, Gross W, Guillevin L, Hoffman G, Jayne D, Jennette J . Granulomatosis with polyangiitis (Wegener's): an alternative name for Wegener's granulomatosis. Arthritis Rheum. 2011; 63(4):863-4. DOI: 10.1002/art.30286. View

5.
Jennette J, Falk R, Hu P, Xiao H . Pathogenesis of antineutrophil cytoplasmic autoantibody-associated small-vessel vasculitis. Annu Rev Pathol. 2013; 8:139-60. PMC: 5507606. DOI: 10.1146/annurev-pathol-011811-132453. View