This is the first study to classify the NCP according to the CT imaging distribution with a relatively larger sample than previous case reports or researches [5,6,7,8,9,10]. The CT examination was performed and the CT signs were analyzed within 1 to 20 days after symptoms. Moreover, the follow-up CT examination was performed at the time of 3 to 27 days after admission. The initial and follow-up chest CT signs were shown as follows.
Common CT signs of the NCP
Distribution
It includes lobular distribution, subpleural distribution, diffuse distribution, and mixed type. The virus particles are small. After inhaling the virus into the airway, the large airway is seldom invaded by the virus due to its abundant cilia and strong immune function. The virus mainly invades bronchioles, causing bronchiolitis and peripheral inflammation, and then spreads and invades the lung tissue. On CT image, the early manifestation shows GGO density. The virus mainly invades lung interstitium, conforming to the previous literature [11]. In all cases, we did not see obvious thickening of the bronchovascular bundle and the pleura, so we speculated that the main lung interstitium invaded by the virus was the lobular interstitium. Therefore, the image distribution is mainly classified as follows:
-
1)
Lobular distribution: when the virus causes inflammation in the lobular core, it is easy to form globular GGO, and then quickly diffuses to the surrounding area, forming larger globular GGO or patches of lobular distribution. In follow-up CT images, the lesions expanded to the surrounding area, and the distribution was mostly seen in lung outer zone or in the whole lung; the adjacent lesions can fuse during progression. This is one of the most common distribution patterns of the NCP, that is, nodular or patchy GGO distributed in the lobular core and fused finally.
-
2)
Subpleural distribution: due to the better development of pulmonary lobules in peripheral subpleural region with rich blood flow and lymph, the inflammatory response of lung lobular interstitium is more severe. The NCP mainly invades the bronchioles and distal lung tissue, causing inflammatory lesions mainly in the interstitium; thus, the distribution is mainly in the peripheral subpleural region, which is also one of the most common distribution patterns.
-
3)
Diffuse distribution: the lobular distribution and subpleural distribution can overlap. Meanwhile, they progress and merge into a large high-density shadow, which can affect most areas of the bilateral whole lung, that is, diffuse distribution.
Number
The lesions are often multiple; some of them are single (at very early stage) and turn into multiple at follow-up. Multiple lesions can develop and fuse rapidly. Although the single case is rare, it is easy to be misdiagnosed, which needs more attention and follow-up.
Density
There are three kinds of density: (1) GGO, (2) consolidation, and (3) GGO + consolidation. We think that marginal fuzzy GGO often appears at the early stage because of the obvious inflammatory exudation; when the exudation turns into the proliferation, fuzzy GGO will become clear GGO, then the consolidation appears with straight edge, which is similar to acute respiratory distress syndrome (ARDS) from the exudative phase to the proliferative phase. At the late stage, the repair was accompanied by the formation of organization, and the contracted edge appears in the consolidation with the fiber traction and bronchiectasis. The contracted edge indicates the recovery of the lesion.
Other accompanying signs
“Parallel pleura sign”
This CT sign is reported for the first time in the current study, which needs two conditions: the first is the subpleural distribution; the second is that the maximum diameter of the lesion is parallel to the pleura. Its formation mechanism may be as follows: When the virus mainly invades the interlobular interstitium, especially the perialveolar interstitium, this part of lymph drainage direction is subpleural and interlobular septum. The lesion will spread to the pleural side and bilateral interlobular septum. Since the distal end is limited by the pleura, the lesion can only cling to the pleura, spread along the reticular structure of the interlobular septum, and diffuse to the periphery. The fusion with subpleural lesions leads to the long axis of the lesions parallel to the pleura. The “parallel pleura sign” is very characteristic in NCP but is not specific; it can be present in other interstitial lung diseases such as influenza pneumonia.
“Paving stone sign”
The “paving stone sign” is an important sign of the NCP, indicating that the virus is mainly involved in the interlobular septum, consistent with the other viral pneumonia, such as severe acute respiratory syndrome (SARS) [12, 13] and Middle East respiratory syndrome (MERS) [14]. However, this sign was nonspecific with other viral pneumonia.
SARS and MERS progress faster than COVID-19 with a longer incubation period, and therefore have higher infectiousness and more asymptomatic infections. They have similar CT manifestations as peripheral multifocal airspace opacities (GGO, consolidation, or both). In addition, the prognosis of COVID-19 is better with milder symptom and fewer lung fibrosis compared with SARS and MER [15].
Air bronchogram and bronchiectasis
The air bronchogram could be observed and no bronchial obstruction was found, due to the fact that the virus is mainly involved in lung interstitium and there was little exudation in the alveoli. Moreover, in all cases, there was no obvious thickening of the bronchial wall. One case had “tree-bud sign,” which can appear at the early stage of viral pneumonia [11], but we think that “tree-bud sign” is not a typical imaging manifestation of the NCP. Bronchiectasis can be found at the later stage, often accompanied by marginal contraction, suggesting that the lesion is at the repair stage caused by fiber traction. Air bronchogram is not specific to COVID-19, but it helps distinguish the virus from other bacterial pneumonia. Bronchiectasis is also very common and not specific to COVID-19, but it helps indicate the progress of the disease.
Vascular sign
Thickening vessels can appear in the lesions, which is consistent with the general rule of inflammation. The inflammation may cause increased vascular permeability, telangiectasia, and relevant pulmonary artery thickening. We think that this sign is not specific to distinguish virus from other inflammatory diseases.
“Halo sign” and “reversed halo sign”
The “halo sign” refers to the ground-glass shadow around the mass or nodule, which can be the change of bleeding around the lesion, or the spread of the lesion to the surrounding interstitium. This sign has been reported in fungi, vasculitis, and some viruses, the most common one is herpes virus [11], and can also be found in COVID-19. On the contrary, the “reversed halo sign” is focal, round, or half-moon shaped, with a GGO area in the center and completely or more than 3/4 surrounded by high-density consolidation, which was first reported in the cryptogenic organizing pneumonia (COP) [16]. This sign can be present in many other diseases such as COP, tuberculosis, vasculitis, lung cancer, and metastasis. The NCP also presented a reversed halo sign. We suggest that the main inflammatory repair is the edge of the lesions, leading to the result that the formation of the edge tends to solid strip shadow while the central repair is relatively delayed.
Follow-up CT changes
Among 35 follow-up cases, the CT manifestations in 20 cases who turned better were mainly shown as follows: (1) The area and the number of GGO or consolidation decreased; (2) the density of GGO increased and turned into consolidation; (3) the edge of consolidation became straight, even contracted or retracted; (4) there were fiber strips or subpleural line. We hypothesize that the development of the GGO into consolidation may be due to secondary alveolar pulmonary edema, and tissue organization, and partly combined with bacterial infection. In addition, the absorption of GGO, consolidation, edge contraction and retraction, fiber strips or subpleural line, and bronchiectasis all indicate the organization changes. Both GGO and consolidation exist in the transitional period. In addition, some cases showed dynamic CT signs; that is, some lesions got better while the other lesions became enlarged or new lesions appeared. This may be due to the delayed inflammatory response or organization in part of the lung tissue. Of the 35 patients, 14 patients became aggravated, mainly manifesting in the increased lesion area and number, and the tendency of fusion. In addition, there were 8 cases of “white lung” changes in diffuse whole lung, which had a high mortality rate.
The limitations in the current study must be acknowledged. This study was performed at a stage that was not sufficiently familiar with the disease. Because of the panic for unknown disease, follow-up CT examinations were too frequent and may cause harm to patients. Although CT examination is helpful for early diagnosis, but follow-up CT is not necessary and even should be avoided especially for patients with mild symptom. Moreover, we used conventional radiation doses for CT scans and low-dose scans should be performed during follow-up CT examinations.
In summary, the CT signs of the NCP have some characteristics. It is mainly distributed in the lobular core, subpleural and diffused bilaterally, including the “parallel pleura sign,” “paving stone sign,” and “reversed halo sign”. The NCP was classified according to the distribution characteristics and “parallel pleura sign” was raised for the first time in this study. During the follow-up, the distribution of lobular core, the fusion of lesions, and the organization changes at late stage will appear. It has been reported that patients with positive chest CT findings may present with false negative results of nucleic acid examination for COVID-19 [17, 18]. Therefore, patients with negative nucleic acid results but highly suspicious CT signs should also be isolated in time. Furthermore, follow-up X-ray or CT examinations are necessary in a short period of time, and those with highly suspicious clinical and radiological manifestations should have multiple nucleic acid tests.