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      Which is your diagnosis? Translated title: Qual o seu diagnóstico?

      case-report

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          Abstract

          A 26-year-old male patient, drugs user, presenting with dry cough and fever for two weeks. The patient has a diagnosis of acquired immunodeficiency syndrome (AIDS), with poor adherence to the treatment. His CD4 count was 20 cells/mm3 and the viral load was 495,208 cps/ml. Chest radiography demonstrated opacity in the right upper lobe of the lung. Chest computed tomography was performed (Figure 1). Figure 1 Computed tomography with window for pulmonary parenchyma. Section at the level of the carina Image description Figure 1. Chest computed tomography shows cavitated consolidation in the right upper lobe of the lung. Also, one observes small nodules and ground glass opacities adjacent to the described image as well as in the contralateral lung. Diagnosis: Rhodococcus equi pneumonia in an AIDS patient. Open biopsy was performed and culture demonstrated bacterial growth. COMMENTS R. equi is a Gram-positive cocci that commonly causes infection in horses and other animals. R. equi infection is rarely found in humans(1), affecting particularly individuals at advanced degree of immunodeficiency. About 80% of cases occur in AIDS patients, most of times in those presenting CD4 lymphocyte count lower than 200 cell/mm3(2,3). In humans, the main infection site is the lung(1). The most frequent clinical presentation is a slow-growing pneumonic process, with cough, fever and constitutional symptoms. R. equi represents a frequent cause of bacteremia and extra-pulmonary signs may be found. The etiological agent can be easily isolated from the sites of infection(2). The main pattern of lung involvement is that of masses with heterogeneous contrast impregnation or foci of pulmonary consolidation intermingled with air bronchograms, either with or without cavitated lesions. Although cavitation may be not present at the moment of the diagnosis, it ends up developing along the disease progression(4). Other findings include ground glass opacities, air-space nodules, small nodules with predominantly centrilobular distribution and the tree-in-bud pattern predominantly located around consolidations. Probably, such findings represent bronchogenic dissemination of the infection. Mediastinal lymph nodes enlargement may be present(1,2,4-8). The typical histopathological finding of R. equi infection corresponds to necrotizing cavitation or soft tissue mass composed of a dense histiocytic infiltrate with abundant eosinophilic granular cytoplasm. Polymorphonuclear leukocytes are numerous in disseminated microabscesses. Periodic acid Schiff staining demonstrates highly positive histiocytes similar to those observed in Whipple's disease. Gram-positive cocci are easy demonstrated at Gram tissue stain. Pulmonary malakoplakia is another finding described in R. equi infection(9). The differential diagnoses for pulmonary R. equi infection in AIDS patients include cavitated infections (tuberculosis, nocardiosis, fungal diseases, lung abscess), lung neoplasms, and more remotely Pneumocystis jiroveci pneumonia (7,10,11). Micobacterium tuberculosis infection, however, is the main differential diagnosis to be considered for patients with R. equi pneumonia, since both bacilli are alcohol-acid resistant. The diagnosis of disease activity in patients with pulmonary tuberculosis depends on multiple factors, namely, clinical signs, physical examination, tuberculin test results and, mainly, detection of the bacillus in sputum, bronchoalveolar lavage, transtracheal aspirate or in lung biopsy specimen, being reinforced by other factors such as sequential alterations at serial chest radiography and previous history of antituberculosis therapy. However, the diagnosis may be difficult considering the facts that sputum bacilloscopy may be negative in 21-66% of cases and it may take up to six weeks for a bacillus colony to grow in a culture, and that findings at chest radiography are frequently classified as indeterminate(12-14). High-resolution computed tomography (HRCT) has shown to be superior to plain radiography in the detection and evaluation of extent of parenchymal alterations, considering that because of its effectiveness in the evaluation of the secondary lung lobe, it allows for a better characterization of pathological pulmonary processes. A recent series of studies published by Brazilian authors(15-23) corroborates such assertion. Thus, HRCT plays an extremely relevant role in the diagnosis of pulmonary tuberculosis. HRCT findings in patients with post-primary tuberculosis include centrilobular nodules, air space nodules, nodular opacities, tree-in-bud pattern, miliary nodules, consolidations, cavitations, bronchial walls thickening, tuberculomas, calcifications, parenchymal bands, interlobular septal thickening, ground glass opacities, pericicatricial emphysema and fibrotic alterations(12,13,24-32). Other manifestations recently described include reversed halo sign and clusters of micronodules, either with or without confluence(33-35). Most of such findings can also be observed in patients with R. equi pneumonia. In conclusion, R. equi infection should be considered in the differential diagnosis of cavitated consolidations in AIDS patients, with a particular difficult differentiation from lesions caused by tuberculosis.

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          Most cited references107

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          Pulmonary tuberculosis: CT findings--early active disease and sequential change with antituberculous therapy.

          To evaluate findings of active pulmonary tuberculosis on computed tomographic (CT) scans and their sequential changes before and after antituberculous chemotherapy, 29 patients with newly diagnosed pulmonary tuberculosis and 12 patients with recent reactivation were studied prospectively. The diagnosis of active pulmonary tuberculosis was based on positive acid-fast bacilli in sputum (n = 29) and changes on serial radiographs obtained during treatment (n = 12). Twenty-six patients were followed up with CT during treatment for 1-20 months. Lungs from the cadavers of nine other patients, who died of pulmonary tuberculosis, were studied to provide a pathologic basis for diagnosis. At examination with CT, centrilobular lesions (nodules or branching linear structures 2-4 mm in diameter) were most commonly seen (n = 39 [95%]); in the 26 patients with follow-up, most of these lesions disappeared within 5 months after the start of treatment. In 11 of 12 patients with recent reactivation, CT clearly differentiated old fibrotic lesions from new active lesions. Lesions in and around the small airways appear to be the most characteristic CT feature of early active tuberculosis and may be a reliable criterion for disease activity.
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            Pulmonary tuberculosis: up-to-date imaging and management.

            S Lee, A Jeong (2008)
            Pulmonary tuberculosis (TB) is a common worldwide infection and a medical and social problem causing high mortality and morbidity, especially in developing countries. The traditional imaging concept of primary and reactivation TB has been recently challenged, and radiologic features depend on the level of host immunity rather than the elapsed time after the infection. We aimed to elaborate the new concept of the diagnosis and treatment of pulmonary TB, to review the characteristic imaging findings of various forms of pulmonary TB, and to assess the role of CT in the diagnosis and management of pulmonary TB. Fast and more accurate TB testing such as bacterial DNA fingerprinting and whole-blood interferon-gamma assay has been developed. Miliary or disseminated primary pattern or atypical manifestations of pulmonary TB are common in patients with impaired immunity. CT plays an important role in the detection of TB in patients in whom the chest radiograph is normal or inconclusive, in the determination of disease activity, in the detection of complication, and in the management of TB by providing a roadmap for surgical treatment planning. PET scans using 18F-FDG or 11C-choline can sometimes help differentiate tuberculous granuloma from lung malignancy.
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              High resolution computed tomographic findings in pulmonary tuberculosis.

              Although chest radiographs usually provide adequate information for the diagnosis of active pulmonary tuberculosis, minimal exudative tuberculosis can be overlooked on standard chest radiographs. The aim of the present study was to assess the findings of active pulmonary tuberculosis on high resolution computed tomographic (HRCT) scans, and to evaluate their possible use in determining disease activity. Thirty two patients with newly diagnosed active pulmonary tuberculosis and 34 patients with inactive pulmonary tuberculosis were examined. The diagnosis of active pulmonary tuberculosis was based on positive acid fast bacilli in sputum and bronchial washing smears or cultures and/or changes on serial radiographs obtained during treatment. With HRCT scanning centrilobular lesions (n = 29), "tree-in-bud" appearance (n = 23), and macronodules 5-8 mm in diameter (n = 22) were most commonly seen in cases of active pulmonary tuberculosis. HRCT scans showed fibrotic lesions (n = 34), distortion of bronchovascular structures (n = 32), emphysema (n = 28), and bronchiectasis (n = 24) in patients with inactive tuberculosis. Centrilobular densities in and around the small airways and "tree-in-bud" appearances were the most characteristic CT features of disease activity. HRCT scanning clearly differentiated old fibrotic lesions from new active lesions and demonstrated early bronchogenic spread. These findings may be of value in decisions on treatment.
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                Author and article information

                Journal
                Radiol Bras
                Radiol Bras
                Radiol Bras
                Radiologia Brasileira
                Colégio Brasileiro de Radiologia e Diagnóstico por Imagem
                0100-3984
                1678-7099
                May-Jun 2014
                May-Jun 2014
                : 47
                : 3
                : XI-XIII
                Affiliations
                [1 ]Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brasil.
                Author notes
                Mailing Address: Dr. Edson Marchiori. Rua Thomaz Cameron, 438, Valparaíso. Petrópolis, RJ, Brazil, 25685-120. E-mail: edmarchiori@ 123456gmail.com .
                Article
                10.590/0100-3984.2014.47.3qd
                4337138
                25741084
                3d3731f8-f1c0-4e75-815a-b1ba1e421afc
                © Colégio Brasileiro de Radiologia e Diagnóstico por Imagem

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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