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Vasculitesdiagdiferencial 20220511173912
Vasculitesdiagdiferencial 20220511173912
DOI: 10.1002/jgf2.4
REVIEW ARTICLE
KEYWORDS
diagnosis, nomenclature, therapy, vasculitis syndrome
This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any
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© 2017 The Authors. Journal of General and Family Medicine published by John Wiley & Sons Australia, Ltd on behalf of Japan Primary Care Association.
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T A B L E 1 Definition of vasculitides adopted by the 2012 Chapel Hill Consensus Conference on the nomenclature of vasculitis
polyangiitis (MPA). However, in PAN and granulomatosis with poly- to laboratory findings for anti-GBM disease. Although there are
angiitis (GPA), there are cases in which abnormal urinary findings various methods to detect anti-GBM antibody, such as the IIF
appear over time rather than immediately. assay, hemagglutination assay, radioimmunoassay (RIA) method,
3. Biochemical markers: In MPA, PAN, and GPA, renal dysfunction, and enzyme-linked immunoassay (ELISA) method, the RIA and
such as elevation of serum creatinine, a rise in BUN, and a decline ELISA method have superior sensitivity (>95%) and specificity
in creatinine clearance, can be observed. As interstitial pneumonia (>97%).8
is one of representative clinical features in MPA, a rise in KL-6 can 6. Imaging study: Plain radiographs of the chest and paranasal si-
also be seen. nuses, ultrasonography, CT, MRI, and thermography have been
4. Antineutrophil cytoplasmic antibody (ANCA): In MPA and EGPA, it used to confirm abnormal vascular wall structure and blood flow
is common (50%-80% of cases) to detect myeloperoxidase (MPO)- dysfunction. If acute-phase Takayasu disease (TAK) is present,
ANCA (perinuclear [p] staining pattern with an indirect immuno- aortic wall thickening will be densely stained with gadolinium on
fluorescent [IIF] assay, p-ANCA). Antineutrophil cytoplasmic contrast-enhanced MRI. As MRA can clearly outline whether or
antibody testing is usually negative in PAN (<20% ANCA positive). not there are any irregularities, contractions, or occlusion of the
In GPA, proteinase 3 (PR3)-ANCA (cytoplasmic (c) staining pattern vascular walls, this imaging modality is often useful for interpreta-
with IIF assay, c-ANCA) is positive (90%). In recent years, genetic tion of symptoms related to ischemia. Further, it may be possible
5 18
factors, biological environment factors (the induction of neutrophil to localize aortic inflammation using F-fluorodeoxyglucose-
extracellular traps [NETs] from neutrophil caused by bacterial in- positron emission tomography (FDG-PET). Increased glycolytic
fections),6 scientific environment factors (antithyroid drugs, such as metabolism in inflammatory tissues or malignant tumors is the ra-
propylthiouracil,7 atmospheric environmental chemicals such as tionale behind the common use of FDG-PET.9 Diagnostic imaging
silica) have been presumed as causes of ANCA positivity. Detailed studies of the thorax (X-rays, CT, MRI) may show interstitial infil-
history taking via an interview is highly important to distinguish pri- trative shadows in the lung field in a patient with MPA.
mary vasculitis from genetic or environmental factor-associated Granulomatous lesions can also be accompanied by infiltrative
vasculitis in a patient with positive ANCA and equivocal clinical fea- shadows in patients with EGPA and GPA. PAN can cause multiple
tures of vasculitis. microaneurysms and/or contractions in association with inflam-
5. Antiglomerular basement membrane (GBM) antibody: Especially in mation of medium-sized and small arteries. Aneurysms can be fre-
cases exhibiting RPGN and/or alveolar hemorrhage, it is essential quently detected in the branches of the abdominal aorta (eg, renal,
to suspect anti-GBM disease. Serum anti-GBM antibody is specific mesenteric, and hepatic arteries) and can be confirmed via
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76 OKAZAKI et al
1) MTX 6 to 15 mg/wk
Improvement
2) CPA 50 to 100 mg/d PO or
300 mg to 750 mg/m2 IV Reduction in PSL dose
Difficult to reduce
3) CsA 3 mg/kg/d, or
4) AZP 2 mg/kg/d
angiography. However, aneurysms are usually not detected during 2. PAN: Although the typical histological finding of PAN is necrotizing
the acute phase. In some cases, it is possible to detect impaired angiitis, which is characterized by fibrinoid necrosis in the tunica
blood flow using MRA or the ultrasonic Doppler method. However, media, old and new lesions are often observed within the same tis-
in Japan, some physicians tend to avoid conventional angiography sues. By definition, PAN does not include inflammation of the arte-
because of its invasiveness and because PAN can typically be di- rioles, venules, and capillaries, meaning that PAN is not associated
agnosed via biopsy. with glomerulonephritis.
7. Physiological tests: electrocardiography (ECG), pulse-wave detec- 3. MPA: The typical histological finding of MPA is necrotizing angiitis
tion, electroencephalography (EEG), electromyography (EMG), and in arterioles and capillaries in the kidneys, indicating necrotizing
nerve conduction studies are important for the diagnosis of vascu- crescentic glomerulonephritis.
litis syndrome and to classify its severity. EMG and nerve conduc- 4. GPA: A finding of necrotizing granulomatous lesions with giant cells
tion studies are crucial for the diagnosis of latent vasculitis in lesion sites of the upper respiratory tract (eg, nose, paranasal si-
syndrome and to identify appropriate biopsy sites. nuses, and soft palate) is useful for early diagnosis. Various patterns
of glomerulonephritis can also be found in kidney biopsy
specimens.
3.4 | Tissue biopsy
5. EGPA: Biopsy specimens from peripheral nerves, muscles, and
With regard to small-vessel vasculitis, it is essential to test for ANCA lungs with infiltration show vasculitides and granulomas with prom-
and immune complexes. However, these are definitive factors for inent invasion with eosinophils.
diagnosis; rather, tissue biopsy is the most important diagnostic 6. Anti-GBM Disease: Diffuse crescentic glomerulonephritis is a dis-
method for vasculitic syndrome. If it is necessary to differentiate tinctive feature of this disease. IIF staining can show deposition of
ANCA-associated vasculitis (AAV) from immune complex-mediated IgG and C3 along the glomerular capillary walls.
vasculitis, it is preferable to prepare the materials for IIF staining in 7. IgA vasculitis (IgAV): Necrotizing angiitis can be observed with
advance before conducting the tissue biopsy. Because the primary blood vessels in the area from the papillary layer to the reticular
lesions of TAK are in the aorta and those of Kawasaki disease (KD) layer of the skin. Using immunofluorescent staining, in accordance
are in the coronary arteries, it is not possible to perform a biopsy for with the areas where necrotizing angiitis has occurred, deposition
diagnosis of these diseases. Hence, in such cases, diagnostic imaging of IgA in areas from the vascular endothelial cells to the vascular
study plays a central role in diagnosis. For other primary vasculitis lumen can be observed.
syndromes, biopsy of the affected vessels is the most useful method
for diagnosis. As mentioned above, to diagnose a typical vasculitis syndrome,
Some considerations with regard to tissue biopsy for systemic vas- clinicians must collect patient information via interview, physical
culitis are as follows: examinations, laboratory testing, imaging studies, and histopatho-
logical examination of biopsy specimens. This allows establishment
1. Giant cell arteritis (GCA): A biopsy of the temporal artery is of a diagnosis of vasculitis syndrome based on the classification
essential for diagnosis. As noncontiguous segmental lesions de- criteria. After diagnosis, treatment should commence as soon as
velop in GCA, it is crucial to prepare serial sections of biopsy possible. However, it may require considerable time to establish
specimens.10 a definitive diagnosis of vasculitis syndrome. During the diagnosis
OKAZAKI et al |
77
No Yes
plasmapheresis
No Yes
F I G U R E 3 Induction therapy for remission in polyarteritis nodosa. Revised from reference 3. mPSL, methylprednisolone; PSL, prednisolone;
IVCY, intravenous cyclophosphamide; CY, cyclophosphamide
2. Jennette JC, Folk RJ, Bacon K, et al. 2012 revised International Chapel
4.3 | Treatment for small-vessel vasculitis Hill Consensus Conference nomenclature of vasculitides. Arthritis
Rheum. 2013;65:1–11.
Microscopic polyangiitis is a representative of small-vessel vasculitis
3. Ozaki S, Ando M, Isobe M, et al. Guideline for management of vascu-
with necrotizing angiitis of small vessels (capillaries and arterioles). litis syndrome (JCS2008). Circ J. 2011;75:474–503.
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incidence of ANCA positivity is high (~80%) in patients with MPA. with malignancies: analysis of sixty patients. Arthritis Rheum.
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In Japan, cases of MPO-ANCA are more predominant than those of
5. Lyons PA, Rayner TF, Trivedi S, et al. Genetically distinct subsets
PR3-ANCA.12 In Western countries, there are more positive cases of within ANCA-associated vasculitis. N Engl J Med. 2012;367:214–23.
proteinase 3 (PR3)-ANCA in AAV. Treatment reports regarding AAV 6. Flint SM, McKinney EF, Smith KG. Emerging concepts in the patho-
in Western countries mainly involve cases with positive PR3-ANCA.13 genesis of antineutrophil cytoplasmic antibody-associated vasculitis.
Curr Opin Rheumatol. 2015;27:197–203.
Three groups of the Ministry of Health and Labor’s Research on
7. Nakazawa D, Tomaru U, Suzuki A, et al. Abnormal conformation and
Measures for Intractable Diseases Project in Japan jointly established impaired degradation of propylthiouracil-induced neutrophil extracel-
the clinical practice guidelines for ANCA-associated vasculitis with lular traps: implications of disordered neutrophil extracellular traps in
MPO-ANCA-positive vasculitis. Especially in the JMAAV protocol, a rat model of myeloperoxidase antineutrophil cytoplasmic antibody-
associated vasculitis. Arthritis Rheum. 2012;64:3779–87.
AAV is classified into three separate categories: mild cases (renal lim-
8. Greco A, Rizzo MI, De Virgilio A, et al. Goodpasture’s syndrome: a
ited type, pulmonary fibrosis type), severe cases (systemic vasculitis,
clinical update. Autoimmun Rev. 2015;14:246–53.
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most severe cases (diffuse alveolar hemorrhage, intestinal perfora- positron emission tomography in the assessment of disease activity in
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Vasculitis syndrome is a rare disease of unknown etiology. In addi- Japanese patients with MPO-ANCA associated vasculitis: JMAAV
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chronic residual peripheral neuropathy in eosinophilic granulomatosis
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CO NFLI CT OF I NTERE S T
of rituximab in 7 Japanese patients with ANCA-associated vasculitis.
The authors have stated explicitly that there are no conflicts of inter- Mod Rheumatol. 2015;25:603–8.
est in connection with this article.