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DOI:10.2214/AJR.05.1065
AJR 2006; 187:1248-1252
© American Roentgen Ray Society


Original Research

High-Resolution CT Findings of 77 Patients with Untreated Pulmonary Paracoccidioidomycosis

Arthur Soares Souza, Jr.1, Emerson Leandro Gasparetto2, Taisa Davaus3, Dante Luiz Escuissato3 and Edson Marchiori2

1 Faculty of Medicine of São José do Rio Preto, São José do Rio Preto, São Paulo, Brazil.
2 University of Rio de Janeiro, Rio de Janeiro, Brazil.
3 University of Paraná, Curitiba, Paraná, Brazil.

Received June 21, 2005; accepted after revision September 29, 2005.

 
Address correspondence to E. L. Gasparetto, R Fernando Amaro 98, ap 61, 80050-020 Curitiba, PR, Brazil.


Abstract
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. The objective of our study was to describe the high-resolution CT findings of 77 patients with pulmonary paracoccidioidomycosis (PCM) who had not yet been treated for PCM.

MATERIALS AND METHODS. The high-resolution CT scans of 77 consecutive patients with proven pulmonary PCM were reviewed by two chest radiologists, and decisions regarding the CT findings were reached by consensus. Seventy-one of the patients were men and six were women, with an average age of 49 years. The criteria for interpretation of the high-resolution CT scans are defined in the Fleischner Society's Glossary of Terms.

RESULTS. The most frequent high-resolution CT findings were ground-glass attenuation areas (58.4%), small centrilobular nodules (45.5%), cavitated nodules (42.9%), large nodules (41.6%), parenchymal bands (33.8%), areas of cicatricial emphysema (33.8%), interlobular septal thickening (31.2%), and architectural distortion (29.9%). Most of these high-resolution CT findings predominated at the periphery (53%) and posterior (88%) regions involving all lung zones, with discrete predominance in the middle zones (35%).

CONCLUSION. The high-resolution CT findings of patients with pulmonary PCM who have not yet been treated consist of ground-glass attenuation areas associated with small centrilobular nodules, cavitated nodules, large nodules, parenchymal bands, and areas of cicatricial emphysema. These abnormalities are usually distributed in the posterior and peripheral regions of the lungs, with discrete predominance in the middle lung zones.

Keywords: chest • high-resolution CT • infectious diseases • lung diseases • pulmonary paracoccidioidomycosis


Introduction
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Paracoccidioidomycosis (PCM) is the most frequent endemic systemic mycosis in Latin America, particularly in Brazil, Argentina, Colombia, and Venezuela [1, 2]. The infection is caused by Paracoccidioides brasiliensis organisms, a dimorphic fungus that grows as budding yeast in tissue and as yeast or mold in culture medium. The disease is acquired by inhalation of infectious particles that reach the lungs and develop the primary infection [3]. Initially, the disease presents with no significant symptoms, but some cases may progress to severe pulmonary involvement [4, 5]. The lungs are the main target organ of P. brasiliensis organisms, and infection of the lungs is the leading cause of morbidity and mortality in patients with PCM [1, 6, 7]. Active pulmonary involvement and residual fibrotic lesions have been reported in 80% and 60% of patients with PCM, respectively [6].

High-resolution CT is frequently performed in the investigation of pulmonary infections, including PCM [4, 7-10]. However, the few studies that have investigated the high-resolution CT findings of PCM included patients who had been treated for PCM before the CT scans were obtained [4, 7, 8]. Those studies showed that interlobular septal thickening, ground-glass opacities, nodules, peribronchovascular interstitial thickening, and traction bronchiectasis were the most common high-resolution CT features of PCM [4, 7]. However, there are no studies, to our knowledge, that have investigated the high-resolution CT findings of patients with pulmonary PCM who had not been treated for PCM before undergoing scanning. Recognition of CT patterns associated with pulmonary PCM could help in the early diagnosis of PCM and in the institution of a specific treatment for PCM, so lung damage caused by the disease can be avoided.

The aim of this study was to present the high-resolution CT findings of 77 patients with pulmonary PCM who had not been treated previously for PCM.


Materials and Methods
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
This study retrospectively analyzed the high-resolution CT scans of 77 consecutive patients with proven pulmonary PCM who underwent high-resolution CT at our hospitals. None of the patients had received any modality of treatment for pulmonary PCM before undergoing CT. There were 71 (92.2%) men and six (7.8%) women who ranged in age from 29 to 75 years (median, 49 years). All patients were symptomatic, usually presenting with chronic cough, slowly progressive dyspnea, and a low fever. The time that had elapsed between the onset of symptoms and diagnosis of PCM infection ranged from 1 to 12 weeks (median, 3 weeks; SD, 3.54 weeks). The diagnosis of P. brasiliensis infection was made at bronchoalveolar lavage (n = 28), bronchial or transbronchial biopsy (n = 24), or surgical lung biopsy (n = 25) (or a combination of these techniques).


Figure 1
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Fig. 1 High-resolution CT scan at level of inferior lobes shows interlobular septal thickening and multiple small centrilobular nodules, some of which have tree-in-bud pattern, in 35-year-old man with pulmonary paracoccidioidomycosis.

 


Figure 2
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Fig. 2 High-resolution CT scan at level of carina shows multiple nodules and masses in 61-year-old man with pulmonary paracoccidioidomycosis. Associated cavitated mass is seen in left lung.

 


Figure 3
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Fig. 3 High-resolution CT scan at level of carina shows subsegmental multifocal consolidations in 42-year-old man with pulmonary paracoccidioidomycosis.

 


Figure 4
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Fig. 4 High-resolution CT scan at level of inferior lobes shows diffuse ground-glass opacities associated with areas of reduced parenchyma attenuation in 37-year-old man with pulmonary paracoccidioidomycosis. In addition, irregular interlobular septal thickening with architectural distortion is identified.

 
The CT scans were obtained at end-inspiration using a 1- or 2-mm collimation at 10-mm intervals and were reconstructed with a high-spatial-frequency algorithm (Somaton ART, Siemens Medical Solutions; and Xvision, Toshiba). The images were photographed at mediastinal (width, 350-450 H; level, 15-25 H) and lung (width, 1,400-1,600 H; level, -600 to 800 H) window settings.

The films were studied by two chest radiologists, and decisions regarding the findings were reached by consensus. The following high-resolution CT features were analyzed: air-space consolidation, ground-glass attenuation, nodules (characterized as large [> 10 mm]; small [< 10 mm] centrilobular; or random), cavitated nodules, "reversed halo sign," tree-in-bud opacities, interlobular or intralobular septal thickening, peribronchovascular or bronchial wall thickening, bronchiectasis, parenchymal bands, architectural distortion, cysts, and areas of low attenuation (cicatricial emphysema). Criteria for these findings are defined in the Fleischner Society's Glossary of Terms [9]. Each one of these findings was analyzed concerning its distribution in the lung parenchyma (central, peripheral, or both; anterior, posterior, or both; and upper, middle, or lower zone or a combination of zones). Lymph node enlargement, pleural effusions, and any other lung abnormalities were also studied.


Figure 5
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Fig. 5 High-resolution CT scan at inferior pulmonary veins shows multifocal ground-glass attenuation areas, nodules with halo sign, and "reversed halo sign" at left lung in 55-year-old man with pulmonary paracoccidioidomycosis.

 


Figure 6
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Fig. 6 High-resolution CT scan at level of inferior pulmonary veins shows random nodules with halo sign, cavitated nodules, and cavitated mass at left inferior lobe in 57-year-old man with pulmonary paracoccidioidomycosis.

 

Results
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
All the patients in this study had abnormal findings on high-resolution CT scans. The most frequent findings were ground-glass attenuation areas (58.4%, n = 45), small centrilobular nodules (45.5%, n = 35), cavitated nodules (42.9%, n = 33), large nodules (41.6%, n =32), parenchymal bands (33.8%, n = 26), areas of cicatricial emphysema (33.8%, n = 26), interlobular septal thickening (31.2%, n = 24), and architectural distortion (29.9%, n = 23) (Figs. 1, 2, 3, 4, 5, 6, 7). Mediastinal lymph node enlargement was seen in 10 patients and pleural effusions in two cases. The most common high-resolution CT findings and their distribution are detailed in Table 1.


Figure 7
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Fig. 7 High-resolution CT scan at level of inferior lobes shows multiple ground-glass attenuation balls, "reversed halo sign," and cavitated nodule with halo sign at posterior region of right lung in 48-year-old man with pulmonary paracoccidioidomycosis.

 

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TABLE 1: Summary of the Most Common High-Resolution CT Findings in Patients with Pulmonary Paracoccidioidomycosis and Their Distribution in the Lungs

 

Patients with pulmonary PCM frequently present with several high-resolution CT features, but a predominant high-resolution CT abnormality was defined in each case. The most frequent predominant findings were ground-glass attenuation areas (32.5%, n = 25), small centrilobular nodules (15.6%, n = 12), large nodules (15.6%, n = 12), and the reversed halo sign (6.5%, n = 5).

Abnormal high-resolution CT findings were predominant in the periphery of the lungs in 53% of the cases, in the central and peripheral regions in 29.4%, and in the central lung regions in 17.6% of the patients. Concerning the anterior and posterior lung zones, most of the abnormalities predominated posteriorly (88%, n = 15), and the remaining two (12%) involved similar amounts of anterior and posterior lung regions. Finally, in 35% of the cases, the features predominated in the middle lung zones; in 23%, in the inferior; and in 6%, in the superior lung regions. The superior and middle lung zones were similarly involved in 18% of the cases, as well as the middle and inferior lung areas (18%).


Discussion
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
PCM, or South American blastomycosis, is an important systemic mycosis in Latin America [2]. The most severe endemic areas of PCM in the world are in the subtropical regions of Brazil. In those endemic areas, PCM is estimated to affect up to 10% of the population, being particularly prevalent in farm workers [3, 4]. The etiologic agent, P. brasiliensis, is an aerobic dimorphic fungus with an unknown habitat [6]. The disease is acquired by inhalation of infective particles that cause a self-limited inflammatory parenchymal lung infection [5]. The initial lesion is similar to the primary complex of tuberculosis, and it is controlled by natural defensive mechanisms or it progresses to symptomatic disease. Following this primary complex, the fungus can spread by lymphatic or blood circulation to the kidneys, spleen, liver, bone, adrenal glands, and CNS [2]. The lung is the organ most commonly affected (50-100%) and is the site of lesions associated with the acute and chronic forms of infection [2, 6].

Few studies have aimed to present the high-resolution CT findings of patients with pulmonary PCM [4, 7, 8]. In addition, the authors of those studies included in their series patients who had been treated for PCM infection before the CT investigation. Muniz et al. [4] analyzed 30 cases of pulmonary PCM, including 16 patients who underwent CT after treatment for PCM had been initiated. The most common high-resolution CT findings in that study included interlobular septal thickening (96.7%), ground-glass opacities (66.7%), nodules (60%), areas of cicatricial emphysema (56.7%), and bronchial wall thickening (46.7%). Funari et al. [7] studied the high-resolution CT findings of the largest series of patients with pulmonary PCM, but those authors included only four patients who had not been treated for PCM infection before undergoing CT. The most common high-resolution CT features in that study were interlobular septal thickening (88%), nodular opacities (83%), traction bronchiectasis (83%), peribronchovascular interstitial thickening (78%), areas of cicatricial emphysema (68%), and centrilobular nodular opacities (63%). These findings showed a predominant bilateral and symmetric distribution, affecting all lung zones.

The most frequent high-resolution CT findings in the present study were ground-glass attenuation areas (58.4%, n = 45), small centrilobular nodules (45.5%, n = 35), cavitated nodules (42.9%, n = 33), large nodules (41.6%, n = 32), parenchymal bands (33.8%, n = 26), areas of cicatricial emphysema (33.8%, n = 26), interlobular septal thickening (31.2%, n = 24), and architectural distortion (29.9%, n = 23). Most of these high-resolution CT findings predominated at the periphery (53%) and posterior (88%) regions involving all lung zones, with discrete predominance in the middle zones (35%). Finally, the most frequent predominant findings were ground-glass attenuation areas (32.5%), small centrilobular nodules (15.6%), and large nodules (15.6%). These patterns and their distribution are different from those reported by Muniz et al. [4] and Funari et al. [7]. These differences can probably be attributed to two factors. First, those authors included in their series patients who had been treated for PCM infection before undergoing CT. The reticular pattern, mainly interlobular septal thickening, that was frequently seen in those studies may be associated with the chronic form of infection and sequelae, thus explaining why those findings were not predominant in our series. Second, although both of the other studies analyzed the high-resolution CT scans based on criteria defined in the Fleischner Society's Glossary of Terms [9], our study protocol was more detailed, including findings that were recommended by the glossary of terms but were not considered by the authors of the other studies.

Funari et al. [7] compared the high-resolution CT findings of two groups of patients in their series: those who received up to 3 months of treatment (n = 16) and those who received more than 3 months of treatment (n = 25). Although this could correct the bias of their study, which included treated and nontreated patients, Funari et al. added four patients who had not received treatment before CT to the group of patients who had received up to 3 months of treatment. The comparison was performed using Fisher's exact test, and p values less than 0.05 were considered statistically significant. The patients who had received less than 3 months of treatment were more likely to present with areas of ground-glass attenuation (p = 0.02), air-space consolidations (p < 0.01), and cavitations (p < 0.01). Comparing our results with those of that study [7], we observe that our findings are more similar to those seen in the group of patients who had received up to 3 months of treatment than those seen in the group who had received more than 3 months of treatment. Parenchymal bands and architectural distortion, although common in our study, were not predominant features, probably indicating that these findings are more frequently representative of chronic pulmonary PCM.

In conclusion, our study shows that the most frequent high-resolution CT findings in patients with pulmonary PCM who had not yet been treated for PCM infection include ground-glass attenuation areas, small centrilobular nodules, cavitated nodules, large nodules, parenchymal bands, and areas of cicatricial emphysema. Most of these high-resolution CT findings predominated at the periphery and posterior regions, involving mainly the middle lung zones. In addition, ground-glass attenuation areas, small centrilobular nodules, and large nodules were the most common predominant high-resolution CT findings in our series. Therefore, we believe that, in the appropriate geographic areas, the diagnosis of PCM should be suggested in patients presenting with these pulmonary CT features so that therapy for the infection can be initiated and, thus, lung damage can be avoided.


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Blotta MH, Mamoni RL, Oliveira SJ, et al. Endemic regions of paracoccidioidomycosis in Brazil: a clinical and epidemiologic study of 584 cases in the southeast region. Am J Trop Med Hyg1999; 61:390 -394[Abstract]
  2. Gasparetto EL, Liu CB, Carvalho Neto A, et al. Central nervous system paracoccidioidomycosis: imaging findings in 17 cases. J Comput Assist Tomogr 2003;27 : 12-17[CrossRef][Medline]
  3. Coutinho ZF, Silva D, Lazéra M, et al. Paracoccidioidomycosis mortality in Brazil (1980-1995). Cad Sáde Pública 2002;18 : 1441-1454
  4. Muniz MAS, Marchiori E, Magnago M, et al. Paracoccidioidomicose pulmonar: aspectos na tomografia computadorizada de alta resolução. Radiol Bras2002; 35:147 -154
  5. Benard G, Kavakama J, Mendes-Giannini MJ, Kono A, Duarte AJ, Shikanai-Yasuda MA. Contribution to the natural history of paracoccidioidomycosis: identification of the primary pulmonary infection in the severe acute form of the disease—a case report. Clin Infect Dis 2005; 40:e1 -e4[CrossRef][Medline]
  6. Tobón AM, Agudelo CA, Osório ML, et al. Residual pulmonary abnormalities in adult patients with chronic paracoccidioidomycosis: prolonged follow-up after itraconazole therapy. Clin Infect Dis 2003; 37:898 -904[CrossRef][Medline]
  7. Funari M, Kavakama J, Shikanai-Yasuda MA, et al. Chronic pulmonary paracoccidioidomycosis (South American blastomycosis): high-resolution CT findings in 41 patients. AJR 1999;173 : 59-64[Abstract/Free Full Text]
  8. Gasparetto EL, Escuissato DL, Davaus T, et al. Reversed halo sign in pulmonary paracoccidioidomycosis. AJR2005; 184:1932 -1934[Abstract/Free Full Text]
  9. Webb WR, Müller NL, Naidich DP. High-resolution CT of the lung, 3rd ed. Philadelphia, PA: Lippincott Williams and Wilkins, 2001: 337-344
  10. Austin JHM, Müller NL, Friedman PJ, et al. Glossary of terms for CT of the lungs: recommendations of the Nomenclature Committee of the Fleischner Society. Radiology 1996;200 : 327-331[Free Full Text]

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