PHILIPPE DE FIGUEIREDO BRAGA COLARES

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LIM/09 - Laboratório de Pneumologia, Hospital das Clínicas, Faculdade de Medicina

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Agora exibindo 1 - 10 de 30
  • article 0 Citação(ões) na Scopus
    Idiopathic pulmonary fibrosis: current diagnosis and treatment
    (2023) AMARAL, Alexandre Franco; COLARES, Philippe De Figueiredo Braga; KAIRALLA, Ronaldo Adib
    Idiopathic pulmonary fibrosis (IPF) is a devastating chronic lung disease without a clear recognizable cause. IPF has been at the forefront of new diagnostic algorithms and treatment developments that led to a shift in patients' care in the past decade, indeed influencing the management of fibrotic interstitial lung diseases other than IPF itself. Clinical presentation, pathophysiology, and diagnostic criteria are briefly addressed in this review article. Additionally, evidence regarding the use of antifibrotics beyond the settings of clinical trials, impact of comorbidities, and therapeutic approaches other than pharmacological treatments are discussed in further detail.
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    Pulmonary actinomycosis in Brazil: a retrospective case series
    (2018) BEDER, Tomas; SALES, Roberta Karla; OLIVEIRA, Ellen Pierre; COSTA, Felipe Marques; COLARES, Philippe Figueiredo Braga; COSTA, Andre Nathan
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    A Rare Association Between Pulmonary Idiopathic Diffuse Neuroendocrine Hyperplasia and Organizing Pneumonia
    (2019) TAKIZAWA, D. B.; COLARES, P. F.; COSTA, F. M. da; BALDI, B. G.; KAIRALLA, R. A.; CARVALHO, C. R. R.
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    Brazilian Analysis of Lent Score: Predicting the Survival Rate of Malignant Pleural Effusion
    (2023) COLARES, P. F.; RIVAS, J. Delgado; BELON, C. E. F.; ACENCIO, M. M. P.; SALES, R. K.; TEIXEIRA, L. R.
  • article 0 Citação(ões) na Scopus
    Tuberculous empyema: combined intrapleural therapy might be an alternative
    (2022) COLARES, Philippe de Figueiredo Braga; RIVAS, Jennifer Kiara Delgado; SCIORTINO, Amanda dos Santos; SALES, Roberta Karla Barbosa de; TEIXEIRA, Lisete Ribeiro
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    Tuberculous Empyema: Combined Intrapleural Therapy Might Be an Alternative
    (2023) COLARES, P. F.; RIVAS, J. Delgado; SCIORTINO, A. D.; SAAVEDRA, N. Medina; SALES, R.; TEIXEIRA, L. R.
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    Primary Lung Fibrous Histiocytoma Presenting as Diffuse Pulmonary Cystic Disease
    (2020) MAIA, A. P.; MARTIN, S. R. San; BRIDI, G. P.; BEDER, T. N.; COLARES, P. F.; HOLZ, I. M.; SERRA, J. P.; NASCIMENTO, E. C. T.; LIMA, L. G. C. A.; AMARAL, A. F.; OLIVEIRA, M. R.; BALDI, B. G.; KAIRALLA, R. A.
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    Adult Patient with Pulmonary Hemosiderosis and Celiac Disease (Lane Hamilton Syndrome): A Case Report
    (2021) ZIMMERMANN, N. A.; COLARES, P. F.; HOLZ, I. M.; AMARAL, A. F.; KAWASSAKI, A. M.; BALDI, B. G.; KAIRALLA, R. A.
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    Dramatic Response of Rituximab in Severe Autoimmune Pulmonary Alveolar Proteinosis: A Case Report
    (2019) COLARES, P. F.; BEDER, T. N.; QUIZHPE, P. J.; CARRANZA, M. X. M.; COSTA, F. M. da; BALDI, B. G.; KAIRALLA, R. A.
  • article 1 Citação(ões) na Scopus
    Mesothelioma in situ with regressive malignant pleural effusion and an unexpected evolution: A case report
    (2022) ALMEIDA, Gustavo C. de; SANTOS, Ubiratan de P.; PARENTE, Yuri de D. M.; COLARES, Philippe de F. B.; MIZUTANI, Rafael F.; BERNARDI, Fabiola del C.; TERRA, Ricardo M.; TERRA-FILHO, Mario
    Malignant pleural mesothelioma (MPM) is an aggressive neoplasm that originates from hyperplasia and metaplasia of the mesothelial cells that cover the pleural cavity. Previous exposure to asbestos is the main risk factor. Since MPM is often diagnosed at an advanced stage with rapid evolution and resistance to treatment, it is associated with an unfavorable outcome. Mesothelioma in situ (MIS) has been postulated as a preinvasive phase of MPM; however, its diagnostic criteria have been defined only recently. Diagnosis of MIS may represent an opportunity for early therapies with better results, but the optimal approach has not been defined thus far. Here, we report on a case of a 74-year-old man with right-sided pleural effusion and a previous history of occupational exposure to asbestos for 9 years who was diagnosed with MIS after a latency of 36 years. During follow-up, spontaneous disease regression was observed 5 months after the initial diagnosis; however, it recurred in the form of invasive epithelioid MPM. There is a paucity of literature on MIS and its evolution; however, our case provides relevant knowledge of this unusual behavior, which is important to define follow-up and therapeutic strategies for future cases.