Page 165 - The Vasculitides, Volume 1: General Considerations and Systemic Vasculitis
P. 165
Nomenclature and Pathologic Features of Vasculitides 141
Conclusion
Many factors must be taken into consideration in rendering an accurate and precise
clinical diagnosis of vasculitis in a given patient, such as the clinical signs and symptoms,
results of laboratory tests, and the observed histopathology of involved organ tissue. The most
important aspects include the types of vessels affected, as for example arteries or venules; the
pathologic features of the inflammatory process such as leukocytoclastic inflammation versus
granulomatous inflammation; immunopathologic features such as IgA-dominant deposits or
paucity of immunoglobulin in vessel walls; serologic findings such as cryoglobulins or
ANCA; associated systemic disease such as RA or SLE; and proximate etiologies such as
HCV and propylthiouracil; as well as, the distribution of lesions to affected organ systems
such as the lungs versus the gut; and any accompanying extravascular lesions such as
necrotizing granulomatosis or aphthous ulcers, and other factors.
References
[1] Jennette, J. C., Falk, R. J., Bacon, P. A., et al. 2012 Revised International Chapel Hill
Consensus Conference Nomenclature of Vasculitides. Arthritis Rheum. 2013; 65:1-11.
[2] Jennette, J. C., Falk, R. J., Andrassy, K., et al. Nomenclature of systemic vasculitides:
The proposal of an international consensus conference. Arthritis Rheum. 1994; 37:187-
192.
[3] Miller, D. V., Maleszewski, J. J. The pathology of large-vessel vasculitides. Clin. Exp.
Rheumatol. 2011; 29 (Suppl. 64):S92-S98.
[4] Churg, J. Large vessel vasculitis. Clin. Exp. Immunol. 1993; 93 (Suppl. 1):11.
[5] Vaideeswar, P., Deshpande, J. R. Pathology of Takayasu arteritis: A brief review. Ann.
Pediatr. Cardiol. 2013; 6:52-58.
[6] Morinaga, A., Ono, K., Komai, K., et al. Microscopic polyangiitis presenting with
temporal arteritis and multiple cranial neuropathies. J. Neurol. Sci. 2007; 2 56:81-83.
[7] Vidal, E., Liozon, F., Rogues, A. M., et al. Concurrent temporal arteritis and Churg-
Strauss syndrome. J. Rheumatol. 1992; 19:1312-1314.
[8] Hamidou, M. A., Moreau, A., Toquet, C., et al. Temporal arteritis associated with
systemic necrotizing vasculitis. J. Rheumatol. 2003; 30: 2165-2169.
[9] Guillevin, L., Lhote, F., Amouroux, J., et al. Antineutrophil cytoplasmic antibodies,
abnormal angiograms and pathological findings in polyarteritis nodosa and Churg-
Strauss syndrome: indications for the classification of vasculitides of the polyarteritis
Nodosa Group. Br. J. Rheumatol. 1996; 35:958-964.
[10] Pagnoux, C., Seror, R., Henegar, C., et al. Clinical features and outcomes in 348
patients with polyarteritis nodosa: a systematic retrospective study of patients
diagnosed between 1963 and 2005 and entered into the French Vasculitis Study Group
Database. Arthritis Rheum. 2010; 62:616-626.
[11] Amano, S., Hazama, F., Hamashima, Y. Pathology of Kawasaki disease: II.
Distribution and incidence of the vascular lesions. Jpn. Circ. J. 1979; 43:741-748.
[12] Amano, S., Hazama, F., Hamashima, Y. Pathology of Kawasaki disease: I. Pathology
and morphogenesis of the vascular changes. Jpn. Circ. J. 1979; 43:633-643.
Complimentary Contributor Copy