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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">COVID-19&#44; a viral disease caused by the SARS-CoV-2&#44; is a lethal infection in a significant number of cases with several clinical manifestations and symptoms&#44; such as lung damage&#44; exacerbated inflammatory response and&#44; in many cases&#44; generalized organ failure&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">1</span></a> To combat these symptoms&#44; one or more immunosuppressive drugs can be used individually or in combination<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">2</span></a>&#59; therefore&#44; the treatment itself can impose an additional risk for the development of fungal infections&#46; It is important to emphasize that there are other associated risk factors&#44; such as malnutrition&#44; prolonged intubation&#44; central and&#47;or arterial venous access&#44; and the need for a nasogastric tube that can increase the chances of mycosis infections in patients suffering from severe cases of COVID-19&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">3</span></a> In the past few decades&#44; the world has experienced an increase in the incidence and spread of emerging fungal infections&#46; This scenario has caused a fundamental change in the epidemiology of invasive fungal diseases&#44; especially in immunocompromised individuals&#44; such as those affected by human immunodeficiency virus &#40;HIV&#41;&#44; cancer&#44; or undergoing transplants&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">4</span></a> Among these emerging pathogens&#44; fungal infections caused by <span class="elsevierStyleItalic">Trichosporon asahii</span> have been identified in neutropenic cancer patients&#44; which significantly increased the severity of their cases leading to a high mortality rate&#46; Recently&#44; the infection has also been identified in other groups of immunocompromised patients&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">5</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Here&#44; we report a case of an immunocompetent patient suffering from a severe case of COVID-19 infection who also developed a triple pulmonary coinfection with <span class="elsevierStyleItalic">Pseudomonas</span> sp&#46;&#44; <span class="elsevierStyleItalic">Stenotrophomonas</span> sp&#46; and <span class="elsevierStyleItalic">Trichosporon</span> sp&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">The patient reported in this study was a 58-year-old male patient that&#44; in 2000&#44; presented a mild chronic kidney disease and had a tuberculosis infection treated with isoniazid chemoprophylaxis&#46; In 2004&#44; he was diagnosed with a bladder neoplasm and was submitted to a radical cystoprostatectomy and a left nephrectomy due to a renal metastasis&#46; The patient had been free of malignant disease for the past ten years and had a competent immune status&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The patient went to the emergency room &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a> &#8211; Day 1&#41; after presenting&#44; for twelve days&#44; high fever&#44; unproductive cough&#44; and general affection&#46; Twenty-four hours before going to the hospital&#44; the patient presented dyspnea with moderate efforts &#40;&#8764;90&#37; SpO<span class="elsevierStyleInf">2</span> at rest&#41;&#46; A blood test confirmed lymphopenia &#40;900&#47;mm<span class="elsevierStyleSup">3</span>&#41;&#44; high C-Reactive Protein &#40;CRP<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>35<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41;&#44; and altered transaminases &#40;Glutamic Oxaloacetic Transaminase &#40;GOT&#41; 160<span class="elsevierStyleHsp" style=""></span>IU&#47;L&#59; Glutamate Pyruvic Transaminase &#40;GPT&#41; IU&#47;L&#59; Gamma Glutamyl Transpeptidase &#40;GGT&#41; 75<span class="elsevierStyleHsp" style=""></span>IU&#47;L&#44; and Phosphatase Alkaline &#40;PAL&#41; 60<span class="elsevierStyleHsp" style=""></span>IU&#47;L&#41;&#46; Chest X-ray images revealed an infiltration in the left base of the lung and the COVID-19 test was positive&#46; With the diagnosis of pneumonia secondary to SARS-CoV-2&#44; the patient was admitted to the Intensive Care Unit &#40;ICU&#41;&#46; A treatment off-label with Hydroxychloroquine sulfate 400<span class="elsevierStyleHsp" style=""></span>mg &#40;equivalent to 310<span class="elsevierStyleHsp" style=""></span>mg base&#41; Q12H for 2 doses&#44; followed by 200<span class="elsevierStyleHsp" style=""></span>mg &#40;&#61;155 base&#41; Q12H for 5 days&#41;&#44; Lopinavir&#47;Ritonavir &#40;400<span class="elsevierStyleHsp" style=""></span>mg&#47;100<span class="elsevierStyleHsp" style=""></span>mg&#41;&#44; Azithromycin &#40;500<span class="elsevierStyleHsp" style=""></span>mg daily for three days&#41;&#44; Methylprednisolone &#40;bolus of 125<span class="elsevierStyleHsp" style=""></span>mg daily for three days&#41;&#44; and Tocilizumab &#40;two doses of 8<span class="elsevierStyleHsp" style=""></span>mg&#47;kg IV &#8211; 8<span class="elsevierStyleHsp" style=""></span>h apart&#41; was prescribed and initiated&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">During hospitalization &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#44; the respiratory function of the patient aggravated and a high oxygen flow &#91;50 LPM and 90&#37; Fraction of Inspired Oxygen &#40;FiO<span class="elsevierStyleInf">2</span>&#41;&#93; was needed&#46; Finally&#44; an orotracheal intubation and an invasive ventilation was needed on the 12th day of hospitalization in the ICU&#46; On the 19th day &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#44; multiresistant <span class="elsevierStyleItalic">Pseudomonas aeruginosa</span> and <span class="elsevierStyleItalic">Stenotrophomonas maltophila</span> strains were isolated from the respiratory secretions of the patient&#46; Despite the treatment with antibiotics&#44; the clinical course of the infection had a poor outcome&#44; and the patient presented persistent fever and hypoxemic respiratory failure&#46; In a chest radiographic exam&#44; left pneumothorax was detected and a chest drainage was performed&#46; A chest CT scan was performed and a suspected pleuro-pulmonary fistula in the lingular zone&#44; a moderate pleural effusion&#44; and bilateral infiltrates were visualized&#46; Following these results&#44; a fiber bronchoscopy was performed in which abundant purulent secretions&#44; mainly in the right bronchial tree&#44; were visualized and aspirated&#46; Endobronchial lesions were not identified&#46; In the collected respiratory secretions&#44; <span class="elsevierStyleItalic">Trichosporon asahii</span> was isolated and a treatment with antifungal drugs &#40;voriconazole&#41; started in day 28th &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The clinical response was weak and the patient developed a septic shock and died on the 38th day after his transfer to the ICU &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The family of the patient authorized the autopsy&#46; The pulmonary autopsy study confirmed the existence of a pattern of acute alveolar damage&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">Every day&#44; a discovery regarding the pathophysiological behavior of SARS-CoV-2 emerges&#46; The SARS-CoV-2 causes a lower respiratory infection which in turn can lead to Acute Respiratory Discomfort Syndromes &#40;ARDS&#41;&#46; In addition to a diffuse alveolar damage with severe inflammatory exudation&#44; patients with COVID-19 can present immunosuppression with decreased CD4&#43;T and CD8&#43; T cells&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">6</span></a> This clinical scenario opens the door for the development of coinfections by opportunistic microorganisms&#46; Within this context&#44; different published reports have shown the importance of assistant doctors and laboratory specialists in verifying the occurrence of potential coinfections&#44; such as aspergillosis&#44; candidiasis&#44; mucormycosis&#44; or cryptococcosis that could lead to co-morbidities in patients with COVID-19&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">7</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">The incidence of invasive infections caused by opportunistic fungal species has increased in recent decades&#46; These fungi are normally difficult to diagnose&#44; resistant to many antifungals&#44; and are associated with high mortality rates&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">8</span></a> In the 1980s&#44; the invasive <span class="elsevierStyleItalic">Trichosporon</span> infection was considered the second most common cause of fungemia among immunosuppressed patients who also suffered from hematological diseases&#44; hemochromatosis&#44; end-stage renal disease&#44; or who were on a long-term corticosteroid treatment&#46; Depending on the age&#44; 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Due to the pandemic situation&#44; informed consent was not requested from the patients&#46; Personal information and data obtained from the subjects were kept confidential&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflict of interest</span><p id="par0050" class="elsevierStylePara elsevierViewall">The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper&#46;</p></span></span>"
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        "texto" => "<p id="par0055" class="elsevierStylePara elsevierViewall">We acknowledge Dr&#46; Barbara Hissa for critical reading and scientific editing of the manuscript&#46; This work was supported by the Brazilian agencies Conselho Nacional de Desenvolvimento Cient&#237;fico e Tecnol&#243;gico &#40;CNPq&#41;&#44; Coordena&#231;&#227;o de Aperfei&#231;oamento de Pessoal de N&#237;vel Superior &#40;CAPES&#41; &#8211; Finance Code 001 and Funda&#231;&#227;o Carlos Chagas Filho de Amparo &#224; Pesquisa do Estado do Rio de Janeiro &#40;FAPERJ&#41;&#46;</p>"
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Scientific Letter
Trichosporon asahii as Cause of Nosocomial Pneumonia in Patient With COVID-19: A Triple Co-infection
Neumonía nosocomial por Trichosporon asahii en un paciente con covid-19: una coinfección triple
Gonzalo Segrelles-Calvoa,b, Glauber R. De S. Araújoc, Estefanía Llopis-Pastora, Susana Frasésc,
Corresponding author
susanafrases@biof.ufrj.br

Corresponding author.
a Servicio de Neumología, Hospital Universitario Rey Juan Carlos, Madrid, Spain
b Instituto de Investigación Biomédica, Fundación Jiménez Díaz, Madrid, Spain
c Laboratório de Biofísica de Fungos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Timeline for an immunocompetent COVID-19 patient who developed an invasive pulmonary trichosporonosis by <span class="elsevierStyleItalic">Trichosporon asahii</span>&#46; The patient was admitted to the intensive care unit on the 12th day after a positive diagnosis by SARS-CoV-2 and died after 24 days&#46; Abbreviations&#58; AZT&#58; Azithromycin HCQ&#58; Hydroxychloroquine sulfate LPN&#47;RTN&#58; Lopinavir&#47;Ritonavir MTP&#58; Methylprednisolone TCZ&#58; Tocilizumab BAS&#58; Bronchial Aspiration CT&#58; Computer Tomography Multi-R&#58; Multi-resistant ICU&#58; Intensive Care Unit CPAP&#58; Continuous Pressure in Upper Airway NIMV&#58; Non-Invasive Mechanical Ventilation&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">COVID-19&#44; a viral disease caused by the SARS-CoV-2&#44; is a lethal infection in a significant number of cases with several clinical manifestations and symptoms&#44; such as lung damage&#44; exacerbated inflammatory response and&#44; in many cases&#44; generalized organ failure&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">1</span></a> To combat these symptoms&#44; one or more immunosuppressive drugs can be used individually or in combination<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">2</span></a>&#59; therefore&#44; the treatment itself can impose an additional risk for the development of fungal infections&#46; It is important to emphasize that there are other associated risk factors&#44; such as malnutrition&#44; prolonged intubation&#44; central and&#47;or arterial venous access&#44; and the need for a nasogastric tube that can increase the chances of mycosis infections in patients suffering from severe cases of COVID-19&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">3</span></a> In the past few decades&#44; the world has experienced an increase in the incidence and spread of emerging fungal infections&#46; This scenario has caused a fundamental change in the epidemiology of invasive fungal diseases&#44; especially in immunocompromised individuals&#44; such as those affected by human immunodeficiency virus &#40;HIV&#41;&#44; cancer&#44; or undergoing transplants&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">4</span></a> Among these emerging pathogens&#44; fungal infections caused by <span class="elsevierStyleItalic">Trichosporon asahii</span> have been identified in neutropenic cancer patients&#44; which significantly increased the severity of their cases leading to a high mortality rate&#46; Recently&#44; the infection has also been identified in other groups of immunocompromised patients&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">5</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Here&#44; we report a case of an immunocompetent patient suffering from a severe case of COVID-19 infection who also developed a triple pulmonary coinfection with <span class="elsevierStyleItalic">Pseudomonas</span> sp&#46;&#44; <span class="elsevierStyleItalic">Stenotrophomonas</span> sp&#46; and <span class="elsevierStyleItalic">Trichosporon</span> sp&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">The patient reported in this study was a 58-year-old male patient that&#44; in 2000&#44; presented a mild chronic kidney disease and had a tuberculosis infection treated with isoniazid chemoprophylaxis&#46; In 2004&#44; he was diagnosed with a bladder neoplasm and was submitted to a radical cystoprostatectomy and a left nephrectomy due to a renal metastasis&#46; The patient had been free of malignant disease for the past ten years and had a competent immune status&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The patient went to the emergency room &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a> &#8211; Day 1&#41; after presenting&#44; for twelve days&#44; high fever&#44; unproductive cough&#44; and general affection&#46; Twenty-four hours before going to the hospital&#44; the patient presented dyspnea with moderate efforts &#40;&#8764;90&#37; SpO<span class="elsevierStyleInf">2</span> at rest&#41;&#46; A blood test confirmed lymphopenia &#40;900&#47;mm<span class="elsevierStyleSup">3</span>&#41;&#44; high C-Reactive Protein &#40;CRP<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>35<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41;&#44; and altered transaminases &#40;Glutamic Oxaloacetic Transaminase &#40;GOT&#41; 160<span class="elsevierStyleHsp" style=""></span>IU&#47;L&#59; Glutamate Pyruvic Transaminase &#40;GPT&#41; IU&#47;L&#59; Gamma Glutamyl Transpeptidase &#40;GGT&#41; 75<span class="elsevierStyleHsp" style=""></span>IU&#47;L&#44; and Phosphatase Alkaline &#40;PAL&#41; 60<span class="elsevierStyleHsp" style=""></span>IU&#47;L&#41;&#46; Chest X-ray images revealed an infiltration in the left base of the lung and the COVID-19 test was positive&#46; With the diagnosis of pneumonia secondary to SARS-CoV-2&#44; the patient was admitted to the Intensive Care Unit &#40;ICU&#41;&#46; A treatment off-label with Hydroxychloroquine sulfate 400<span class="elsevierStyleHsp" style=""></span>mg &#40;equivalent to 310<span class="elsevierStyleHsp" style=""></span>mg base&#41; Q12H for 2 doses&#44; followed by 200<span class="elsevierStyleHsp" style=""></span>mg &#40;&#61;155 base&#41; Q12H for 5 days&#41;&#44; Lopinavir&#47;Ritonavir &#40;400<span class="elsevierStyleHsp" style=""></span>mg&#47;100<span class="elsevierStyleHsp" style=""></span>mg&#41;&#44; Azithromycin &#40;500<span class="elsevierStyleHsp" style=""></span>mg daily for three days&#41;&#44; Methylprednisolone &#40;bolus of 125<span class="elsevierStyleHsp" style=""></span>mg daily for three days&#41;&#44; and Tocilizumab &#40;two doses of 8<span class="elsevierStyleHsp" style=""></span>mg&#47;kg IV &#8211; 8<span class="elsevierStyleHsp" style=""></span>h apart&#41; was prescribed and initiated&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">During hospitalization &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#44; the respiratory function of the patient aggravated and a high oxygen flow &#91;50 LPM and 90&#37; Fraction of Inspired Oxygen &#40;FiO<span class="elsevierStyleInf">2</span>&#41;&#93; was needed&#46; Finally&#44; an orotracheal intubation and an invasive ventilation was needed on the 12th day of hospitalization in the ICU&#46; On the 19th day &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#44; multiresistant <span class="elsevierStyleItalic">Pseudomonas aeruginosa</span> and <span class="elsevierStyleItalic">Stenotrophomonas maltophila</span> strains were isolated from the respiratory secretions of the patient&#46; Despite the treatment with antibiotics&#44; the clinical course of the infection had a poor outcome&#44; and the patient presented persistent fever and hypoxemic respiratory failure&#46; In a chest radiographic exam&#44; left pneumothorax was detected and a chest drainage was performed&#46; A chest CT scan was performed and a suspected pleuro-pulmonary fistula in the lingular zone&#44; a moderate pleural effusion&#44; and bilateral infiltrates were visualized&#46; Following these results&#44; a fiber bronchoscopy was performed in which abundant purulent secretions&#44; mainly in the right bronchial tree&#44; were visualized and aspirated&#46; Endobronchial lesions were not identified&#46; In the collected respiratory secretions&#44; <span class="elsevierStyleItalic">Trichosporon asahii</span> was isolated and a treatment with antifungal drugs &#40;voriconazole&#41; started in day 28th &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The clinical response was weak and the patient developed a septic shock and died on the 38th day after his transfer to the ICU &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The family of the patient authorized the autopsy&#46; The pulmonary autopsy study confirmed the existence of a pattern of acute alveolar damage&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">Every day&#44; a discovery regarding the pathophysiological behavior of SARS-CoV-2 emerges&#46; The SARS-CoV-2 causes a lower respiratory infection which in turn can lead to Acute Respiratory Discomfort Syndromes &#40;ARDS&#41;&#46; In addition to a diffuse alveolar damage with severe inflammatory exudation&#44; patients with COVID-19 can present immunosuppression with decreased CD4&#43;T and CD8&#43; T cells&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">6</span></a> This clinical scenario opens the door for the development of coinfections by opportunistic microorganisms&#46; Within this context&#44; different published reports have shown the importance of assistant doctors and laboratory specialists in verifying the occurrence of potential coinfections&#44; such as aspergillosis&#44; candidiasis&#44; mucormycosis&#44; or cryptococcosis that could lead to co-morbidities in patients with COVID-19&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">7</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">The incidence of invasive infections caused by opportunistic fungal species has increased in recent decades&#46; These fungi are normally difficult to diagnose&#44; resistant to many antifungals&#44; and are associated with high mortality rates&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">8</span></a> In the 1980s&#44; the invasive <span class="elsevierStyleItalic">Trichosporon</span> infection was considered the second most common cause of fungemia among immunosuppressed patients who also suffered from hematological diseases&#44; hemochromatosis&#44; end-stage renal disease&#44; or who were on a long-term corticosteroid treatment&#46; Depending on the age&#44; underlying conditions&#44; presence of neutropenia&#44; and clinical treatments&#44; the mortality rates of patients suffering from an invasive tricosporonosis infection can range from 30&#37; to 90&#37;&#46;<a class="elsevierStyleCrossRefs" href="#bib0100"><span class="elsevierStyleSup">9&#8211;11</span></a> Until now&#44; our case is the first report that shows a <span class="elsevierStyleItalic">Trichosporon</span> infection in a COVID-19 patient&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">In conclusion&#44; we report a case of a triple pulmonary coinfection in an immunocompetent patient with severe SARS-CoV-2 pneumonia&#46; As the pandemic continues to spread around the world&#44; other reports to assess the frequency of emergent and reemerging highly resistant bacterial and fungal coinfections in individuals suffering from COVID-19 are needed&#46; These coinfections impose severe complications in COVID-19 patients that might lead to death due to the aggravation in the primary viral condition&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Ethics declarations</span><p id="par0045" class="elsevierStylePara elsevierViewall">The present study was approved by the Ethics Committee of the Fundaci&#243;n Jim&#233;nez D&#237;az Health Research Institute &#40;EO102-20-HRJC&#41;&#46; Due to the pandemic situation&#44; informed consent was not requested from the patients&#46; Personal information and data obtained from the subjects were kept confidential&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflict of interest</span><p id="par0050" class="elsevierStylePara elsevierViewall">The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper&#46;</p></span></span>"
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        "texto" => "<p id="par0055" class="elsevierStylePara elsevierViewall">We acknowledge Dr&#46; Barbara Hissa for critical reading and scientific editing of the manuscript&#46; This work was supported by the Brazilian agencies Conselho Nacional de Desenvolvimento Cient&#237;fico e Tecnol&#243;gico &#40;CNPq&#41;&#44; Coordena&#231;&#227;o de Aperfei&#231;oamento de Pessoal de N&#237;vel Superior &#40;CAPES&#41; &#8211; Finance Code 001 and Funda&#231;&#227;o Carlos Chagas Filho de Amparo &#224; Pesquisa do Estado do Rio de Janeiro &#40;FAPERJ&#41;&#46;</p>"
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ISSN: 03002896
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