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Reversed Halo Sign

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Definition

Reversed halo sign, which was named originally from the disease cryptogenic organizing pneumonia, refers to a focal, rounded area of ground-glass opacity surrounded by a more or less complete ring of consolidation [1, 2] (Fig. 8.1).

Diseases Causing the Sign

The reversed halo sign was Þrst described as being relatively speciÞc for cryptogenic organizing pneumonia (COP) (Fig. 8.2) or COP-like reaction but was later observed in several other infectious and noninfectious diseases. Pulmonary mucormycosis (former pulmonary zygomycosis) (Fig. 8.3) and invasive pulmonary aspergillosis may manifest the reversed halo sign [3]. Other causes of the reversed halo sign include noninvasive fungal infections such as paracoccidioidomycosis, histoplasmosis, and Pneumocystis jirovecii pneumonia [4]. Furthermore, pulmonary infarction [5], antineutrophil cytoplasmic antibodyassociated granulomatous vasculitis (former WegenerÕs granulomatosis), radiofrequency ablation, and lymphomatoid granulomatosis (Fig. 8.4) may also lead to this Þnding [6, 7] (Table 8.1).

Distribution

The reversed halo sign in COP may have its distribution along the subpleural lungs or the bronchovascular bundles [1]. In invasive fungal infection in immunocompromised patients, the sign appears as a large single lesion. In noninvasive fungal infection, the reversed halo sign(s) is usually associated with ground-glass opacity, small centrilobular nodules, or areas of consolidation, and the lesions are usually

bilateral and asymmetric [4]. The reversed halo sign in chronic eosinophilic pneumonia may show upper and mid lung zone predominance, whereas pulmonary infarction may show subpleural location in pulmonary infarction.

Clinical Considerations

In neutropenic patients, the presence of reversed halo sign may suggest invasive fungal infection. Approximately 40 % of patients with chronic eosinophilic pneumonia have asthma; thus, reversed halo sign in asthmatics may imply chronic eosinophilic pneumonia [8]. In the situation of clinically pulmonary embolic disease, the presence of reversed halo sign hints the diagnosis of pulmonary infarction.

Key Points for Differential Diagnosis

1.On CT scans, the reversed halo sign is observed in approximately 20 % of COP patients [1].

2.The reversed halo sign, along with the halo sign, is

highly suggestive of early infection by an angioinvasive fungus; the halo sign and reversed halo sign are most commonly associated with invasive pulmonary aspergillosis and pulmonary mucormycosis, respectively [3].

3. In paracoccidioidomycosis, the reversed halo sign is seen in 10 % of patients with active

Paracoccidioides brasiliensis infection [4].

4.The reversed halo sign Þndings may be speciÞcally useful for making a diagnosis of pulmonary infarction, when direct Þndings of thromboembolism are absent, especially when CT examination is delayed relative to symptom onset [5].

K.S. Lee et al., Radiology Illustrated: Chest Radiology, Radiology Illustrated,

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DOI 10.1007/978-3-642-37096-0_8, © Springer-Verlag Berlin Heidelberg 2014

 

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Reversed Halo Sign

 

 

 

stains

lightly and assumes the round to

oval, elongated,

a

branching shapes in airspaces. The process is sharply demarcated from the adjacent areas of normal parenchyma [9].

Symptoms and Signs

The mean age of COP at presentation is about 50Ð55 years (range 21Ð80 years). The duration of symptoms prior to diagnosis is usually less than 2 months [10]. In typical presentation, it begins with a ßu-like illness characterized by fever, malaise, fatigue, weight loss, and cough, followed by the

b development of dyspnea. The clinical presentation of COP is often confused with that of community-acquired pneumonia. Hemoptysis and Þnger clubbing are rare. Chest auscultation reveals Þne inspiratory crackles in both lower lungs.

CT Findings

The typical CT Þndings also consist of unilateral or bilateral areas of airspace consolidation [11]. In approximately 60 % of cases, the consolidation involves mainly the subpleural or peribronchial lung regions or both [12]. Areas of groundglass opacity are commonly present in association with the

c areas of consolidation. Small, ill-deÞned nodules, often in a centrilobular distribution, are seen in 30Ð50 % of cases [12]. An air bronchogram with traction bronchiectasis may be seen in patients who have extensive consolidation and are usually restricted to these areas. Occasionally, the disease is manifested as a large nodule or mass-like area of consolidation. On CT scans, the reversed halo sign is observed in approximately 20 % of COP patients [1] (Fig. 8.2).

CT–Pathology Comparisons

Fig. 8.1 Reversed halo sign in a 55-year-old asthmatic woman and chronic eosinophilic pneumonia. (aÐc) Lung window images of thinsection (1.5-mm section thickness) scans obtained at levels of the great vessels (a), aortic arch (b), and azygos arch (c), respectively, show multifocal areas of ground-glass opacity in both lungs. Please note reversed halo sign (ground-glass opacity surrounded by a more or less complete ring of consolidation) (arrows) in both upper lobes

Cryptogenic Organizing Pneumonia and

Reversed Halo Sign

Pathology and Pathogenesis

COP is a predominantly airspace-Þlling, active Þbrosing process that involves distal bronchioles, alveolar ducts, and peribronchiolar alveoli in varying proportions (Fig. 8.2). The Þbrosis is easily recognized at low magniÞcation because it

The areas of consolidation correspond histologically to the regions of lung parenchyma that show airspace Þbrosis [13]. The ground-glass opacities correlate with areas of alveolar septal inßammation and minimal airspace Þbrosis. The small nodules are related to foci of organizing pneumonia limited to the peribronchiolar region and/or to Þbroblastic tissue plugs within the bronchiolar lumen. The central groundglass opacity of the reversed halo sign corresponds histopathologically to the area of alveolar septal inßammation and cellular debris, and the ring-shaped peripheral airspace consolidation of the reversed halo sign, to the area of organizing pneumonia within the alveolar ducts [1].

Patient Prognosis

In general, COP improves rapidly with the administration of corticosteroid therapy. Complete recovery with physiologic