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1.
Med Clin (Barc) ; 152(3): 104-106, 2019 02 01.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-29789142

RESUMO

INTRODUCTION: Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH) is a rare disorder characterized by a proliferation of neuroendocrine cells within the lung. It is classically described as a disease with persistent cough, dyspnea and wheezing in non-smoker middle aged females. CT of the chest reveals diffuse air trapping with mosaic pattern. PATIENTS AND METHODS: We present two cases of DIPNECH that were sent to our department to perform a lung biopsy with the diagnostic suspicion of diffuse interstitial disease. Both cases were women with a history of chronic cough and moderate effort dyspnea. RESULTS AND DISCUSSION: The aim of this paper is that physicians take into account this diagnostic entity before treating as an asthmatic a patient with these characteristics, not forgetting that they are prenoplastic lesions.


Assuntos
Pulmão/patologia , Nódulos Pulmonares Múltiplos/patologia , Células Neuroendócrinas/patologia , Lesões Pré-Cancerosas/patologia , Idoso , Asma/complicações , Asma/diagnóstico , Broncoscopia , Fumar Cigarros , Tosse/etiologia , Diagnóstico Diferencial , Dispneia/etiologia , Feminino , Humanos , Hiperplasia , Pulmão/diagnóstico por imagem , Pessoa de Meia-Idade , Nódulos Pulmonares Múltiplos/complicações , Nódulos Pulmonares Múltiplos/diagnóstico por imagem , Tomografia por Emissão de Pósitrons , Lesões Pré-Cancerosas/complicações , Lesões Pré-Cancerosas/diagnóstico , Lesões Pré-Cancerosas/diagnóstico por imagem , Testes de Função Respiratória , Tomografia Computadorizada por Raios X , Doenças de von Willebrand/complicações
2.
Kardiochir Torakochirurgia Pol ; 13(2): 148-9, 2016 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-27516790

RESUMO

Primary pulmonary synovial sarcoma is an extremely rare tumor with an unknown cause. The diagnosis is established after other primary lung malignancies or metastatic extrathoracic sarcoma have been excluded. We report the case of a 69-year-old man who presented with a well-defined mass in the right upper lobe on a chest X-ray. A video-assisted thoracoscopic surgery (VATS) right upper lobectomy was performed. Immunohistochemically, neoplastic cells were positive for vimentin, CD56 and Bcl-2, and focally positive for CD99, epithelial membrane antigen and cytokeratin 7 and 19. The cytogenetic study revealed a SYT genetic reassortment. So, the final pathological diagnosis was primary pulmonary synovial sarcoma.

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