Antineutrophil Cytoplasmic Antibody–Associated Vasculitis

Etiology, Prevalence, and Epidemiology

Pulmonary vasculitis is traditionally characterized by size of vessel involvement as defined by the Chapel Hill nomenclature. Within the small-vessel vasculitides, antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis represents a diverse group of entities, and although the inciting stimulus has not been fully elucidated, an immune-mediated response is implicated.

Although rare, with an overall incidence of 20 to 100 cases per million and a prevalence of 150 to 450 cases per million, pulmonary vasculitis remains one of the most challenging diagnoses and management concerns in the care of critically ill patients. This in part is due to the nonspecific disease manifestations and diagnosis through a combination of clinical and imaging criteria.

Because of the tremendous overlap in clinical and laboratory manifestations among the systemic vasculitides and an absence of validated criteria for diagnosis, determining the exact vasculitis affecting the patient and initiation of the appropriate treatment can be difficult. A recent multinational observational study, endorsed by the American College of Rheumatology and the European League Against Rheumatism, the Diagnostic and Classification Criteria for Vasculitis study (DCVAS) was started, seeking to develop and validate diagnostic and classification criteria for the primary vasculitides.

Three entities are traditionally grouped within the small-vessel vasculitis class, specifically, antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis: granulomatosis with polyangiitis (GPA, formerly Wegener granulomatosis), eosinophilic granulomatosis with polyangiitis (eGPA, formerly Churg-Strauss syndrome), and microscopic polyangiitis (MPA). Antineutrophil cytoplasmic antibodies activate neutrophils and monocytes that express the ANCA antigens myeloperoxidase (MPO) and proteinase 3 (PR3) on their surfaces. Cytoplasmic-pattern ANCA (c-ANCA) targets the MPO antigen, whereas perinuclear-pattern ANCA (p-ANCA) targets PR3.

Although each of these entities is associated with a positive ANCA, GPA is associated with c-ANCA reactivity, eGPA is usually associated with perinuclear p-ANCA activity, and MPA can have c-ANCA or p-ANCA positivity. GPA has an annual incidence of approximately 30 cases per million, whereas eGPA is the least common ANCA-associated vasculitis, with an annual incidence of approximately 2.4 cases per million. MPA has an annual incidence similar to GPA, with 10 to 30 cases per million, and represents the most common cause of pulmonary-renal syndrome.

Granulomatosis With Polyangiitis (Formerly Wegener Granulomatosis)

Clinical Presentation

Formerly referred to as Wegener granulomatosis, GPA may manifest as a systemic disease or involve primarily or exclusively the respiratory tract. This limited GPA is not a distinct process but instead exists along a continuum and often precedes systemic disease.

Most patients present with upper and lower respiratory symptoms, including epistaxis, sinusitis, cough, hemoptysis, dyspnea, and pleuritic chest pain. Systemic symptoms include fever, malaise, weight loss, and fatigue; with joint involvement taking the form of arthralgia or arthritis. Fifty percent to 80% of patients have glomerulonephritis.


Characteristic histopathologic findings consist of granulomatous inflammation with vasculitis and parenchymal necrosis. A mixed cellular infiltrate of neutrophils, lymphocytes, plasma cells, histiocytes, and eosinophils tends to be aggregated in small microabscess-like clusters. As these clusters become necrotic, they enlarge, coalesce, and result in a characteristic appearance of geographic necrosis ( Figs. 46.1 and 46.2 ). Inflammation is typically parenchymal, although mucosal or submucosal granulomatous inflammation of the airways is also common. On occasion, patients may present with or develop capillaritis, which results in focal or diffuse hemorrhage that remains an important cause of morbidity and mortality in patients with GPA.

Fig. 46.1

Granulomatosis with polyangiitis: geographic necrosis. (A) Histologic specimen demonstrates areas of basophilic necrosis with irregular border, resulting in a geographic appearance. The necrotic regions are surrounded by a mixed inflammatory infiltrate. (B) High-power view demonstrates granulomatous inflammation and multinucleated giant cells (arrows) .

(Courtesy Dr. John English, Department of Pathology, Vancouver General Hospital, Canada.)

Fig. 46.2

Granulomatosis with polyangiitis: necrosis and cavitation. Histologic specimen shows nodule with necrosis and cavitation (asterisk).

(Courtesy Dr. John English, Department of Pathology, Vancouver General Hospital, Canada.)

Manifestations of the Disease

Radiography and Computed Tomography

The most common radiographic abnormality consists of lung nodules or masses, seen in up to 90% of patients with GPA ( Fig. 46.3 ). The nodules and masses can range from a few millimeters to greater than 10 cm in diameter. The nodules tend to be bilateral and show no apicobasal gradient. An increase in size and number of nodules is associated with disease progression. Computed tomography (CT) often will show nodules that are not apparent on radiography and is more sensitive for the presence of cavitation, which is evident on CT scan in most nodules larger than 2 cm in diameter ( Fig. 46.4 ). When cavitation occurs, masses tend to be thick walled and have an irregular, shaggy inner lining ( Fig. 46.5 ). In up to 15% of cases, one or more of the nodules or masses are surrounded by a rim of ground-glass opacity representing the CT halo sign ( Fig. 46.6 ). Less commonly, areas of ground-glass opacity can be surrounded by consolidation in the so-called reversed halo sign, which likely represents an organizing pneumonia-like reaction ( Fig. 46.7 ).

Fig. 46.3

Granulomatosis with polyangiitis: bilateral nodules and masses. Chest radiograph demonstrates bilateral nodules, masses, and focal areas of consolidation in a central distribution.

Fig. 46.4

Granulomatosis with polyangiitis: cavitary nodules. (A) Chest radiograph shows bilateral thin-walled cavitary nodules. (B) Coned-down coronal reformatted CT image demonstrates thin-walled left upper lobe cavitary nodule, with mild surrounding ground-glass opacities suggestive of hemorrhage.

Fig. 46.5

Granulomatosis with polyangiitis: cavitating nodules and masses. (A) Posteroanterior chest radiograph shows multiple large thick-walled cavities with air-fluid levels. The left upper lung zone is oligemic, suggesting the possibility of compromise of the left upper lobe bronchus and resulting hypoxic vasoconstriction. (B) Coronal reformatted CT image from a different patient shows a thick-walled cavitary mass in the left upper lobe perihilar region. (C) CT image from the same patient as (B) shows an air-fluid level within the cavitary mass .

(Fig. 46.5A from Müller NL, Fraser RS, Colman NC, Paré PD. Radiologic Diagnosis of Diseases of the Chest . Philadelphia: WB Saunders; 2001.)

Fig. 46.6

Granulomatosis with polyangiitis: CT halo sign. (A) CT image shows peripheral cavitary nodule in the left upper lobe surrounded by a halo of ground-glass opacity. (B) CT image at the level of the minor fissure shows a noncavitary right upper lobe nodule with surrounding halo of ground-glass opacity. Foci of left upper and bilateral lower lobe ground-glass opacities likely represent pulmonary hemorrhage.

Fig. 46.7

Granulomatosis with polyangiitis: reversed halo sign. CT image shows ground-glass opacity with rim of surrounding consolidation. Histopathologic analysis of these types of nodules usually show central hemorrhage and a rim of organizing pneumonia reaction pattern.

Areas of airspace consolidation, or less commonly ground-glass opacities, are seen in approximately 25% to 50% of patients ( Figs. 46.8 to 46.10 ). Foci of cavitation may occasionally be seen within the areas of consolidation. Diffuse consolidation or ground-glass opacities usually reflects the presence of pulmonary hemorrhage and can be seen in up to 10% of patients (see Fig. 46.9 ).

Fig. 46.8

Granulomatosis with polyangiitis: ground-glass opacities and consolidation. Chest radiograph (A) and CT image (B) show asymmetric bilateral ground-glass opacities and areas of consolidation. On CT the consolidation in the left upper lobe has a perilobular distribution of consolidation (arrows) that surrounds ground-glass opacities, a finding consistent with organizing pneumonia secondary to pulmonary hemorrhage.

Fig. 46.9

Granulomatosis with polyangiitis: pulmonary hemorrhage. (A) Chest radiograph shows perihilar predominant consolidation that spares the lung apices and bases. (B) Axial CT image shows perihilar predominant consolidation and ground-glass opacities that spare the lung periphery, which is typical of pulmonary hemorrhage.

(From Lichtenberger JP 3rd, Digumarthy SR, Abbott GF, et al. Diffuse pulmonary hemorrhage: clues to the diagnosis. Curr Probl Diagn Radiol . 2014;43:128–139.)

Fig. 46.10

Granulomatosis with polyangiitis: mass and consolidation before and after treatment. (A) CT image shows a right upper lobe mass (arrowhead) and left upper lobe consolidation (arrow) containing air bronchograms. (B) Repeat CT image 9 months after initiation of treatment demonstrates considerable improvement of the right upper lobe mass (arrowhead) and left upper lobe consolidation (arrow) with residual scarring.

(From Martinez F, Chung J, Digumarthy S, et al. Common and uncommon manifestations of Wegener granulomatosis at chest CT: radiologic-pathologic correlation. Radiographics . 2012;32:51–69.)

Other less common parenchymal abnormalities include centrilobular nodules, tree-in-bud opacities, septal lines, and foci of calcification within the nodules, masses, or areas of consolidation.

Tracheal and bronchial involvement is usually inferred on radiography by secondary signs of airway obstruction, such as atelectasis or air-trapping. When focal airway stenosis is visualized, it most commonly affects the subglottic trachea ( Fig. 46.11 ). With CT central bronchial wall thickening is seen in 50% to 60% of patients and tracheal wall thickening in 15% ( Fig. 46.12 ). Multiplanar reconstructions are essential for optimal imaging assessment of the presence and severity of airway stenosis (see Fig. 46.12 ).

Fig. 46.11

Granulomatosis with polyangiitis: subglottic stenosis. Lateral view of the neck shows focal wall thickening of the subglottic trachea (arrow) with associated stenosis.

Fig. 46.12

Granulomatosis with polyangiitis: tracheal and bronchial stenosis. (A) Unenhanced CT image at the level of the azygos arch shows marked circumferential thickening of the wall of the trachea with associated luminal narrowing. (B) CT image at a lower level demonstrates circumferential thickening of the wall of the left main bronchus causing stenosis. Note associated partial left lower lobe atelectasis. (C) Three-dimensional reformatted image from a virtual bronchoscopy in a different patient shows stenosis (arrows) of the distal trachea and proximal main bronchi.

(Fig. 46.11C from Martinez F, Chung J, Digumarthy S, et al. Common and uncommon manifestations of Wegener granulomatosis at chest CT: radiologic-pathologic correlation. Radiographics . 2012;32:51–69.)

Pleural effusions occur in 15% to 20% of patients and pleural thickening in 10%. Mediastinal lymph node enlargement is seen on CT in approximately 20% of cases and hilar lymph node enlargement in 3%.

Approximately 50% of nodules and masses will resolve completely with disease treatment, and another 40% will decrease in size. However, intralobular linear opacities and areas of bronchiectasis tend to remain stable. This reinforces the theory that ground-glass opacities, consolidation, cavitated nodules, and masses represent active inflammatory lesions, whereas intralobular linear opacities and areas of bronchiectasis more often represent chronic fibrosis. Rarely, hemosiderin can accumulate in the alveoli from repeated hemorrhage, resulting in diffuse centrilobular nodules ( Fig. 46.13 ).

Jul 21, 2019 | Posted by in GENERAL RADIOLOGY | Comments Off on Antineutrophil Cytoplasmic Antibody–Associated Vasculitis
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