Mostrar el registro sencillo del ítem
Paciente femenino de 57 años con fibrosis pulmonar idiopática.
| dc.contributor.advisor | Gaibor Luna, Juan Carlos | |
| dc.contributor.author | Macías Fernández, Estiven Jhosbel | |
| dc.date.accessioned | 2021-06-18T16:02:50Z | |
| dc.date.available | 2021-06-18T16:02:50Z | |
| dc.date.issued | 2021 | |
| dc.identifier.uri | http://dspace.utb.edu.ec/handle/49000/9843 | |
| dc.description | In the present study a case of idiopathic pulmonary fibrosis is described, this pathology is defined as a diffuse interstitial lung disease that affects the correct functioning of the lungs without any specific cause. Idiopathic pulmonary fibrosis in several cases is associated with a poor prognosis that can often put the life of the patient at risk, for this reason it is vitally important to know the symptoms that may occur in the disease in conjunction with the radiological and tomographic signs that can be observed and help to control and manage the disease. We present the case of a 57-year-old female patient, with no medical history or toxic habits, who came to the health center due to the presence of cough, shortness of breath, and yellowish-white expectoration. A respiratory rate of 24 rpm, a heart rate of 110/70, a heart rate of 22 Imp and an oxygen saturation of 94%, a temperature of 36 ° and a body weight of 58kg were admitted to the hospital. A series of complementary tests are performed where the characteristic patterns of idiopathic pulmonary fibrosis are observed. As it is an idiopathic disease, that is, no specific cause is known, it is likely that the symptoms appear suddenly or even worsen. | es_ES |
| dc.description | In the present study a case of idiopathic pulmonary fibrosis is described, this pathology is defined as a diffuse interstitial lung disease that affects the correct functioning of the lungs without any specific cause. Idiopathic pulmonary fibrosis in several cases is associated with a poor prognosis that can often put the life of the patient at risk, for this reason it is vitally important to know the symptoms that may occur in the disease in conjunction with the radiological and tomographic signs that can be observed and help to control and manage the disease. We present the case of a 57-year-old female patient, with no medical history or toxic habits, who came to the health center due to the presence of cough, shortness of breath, and yellowish-white expectoration. A respiratory rate of 24 rpm, a heart rate of 110/70, a heart rate of 22 Imp and an oxygen saturation of 94%, a temperature of 36 ° and a body weight of 58kg were admitted to the hospital. A series of complementary tests are performed where the characteristic patterns of idiopathic pulmonary fibrosis are observed. As it is an idiopathic disease, that is, no specific cause is known, it is likely that the symptoms appear suddenly or even worsen. | es_ES |
| dc.description.abstract | En el presente estudio se describe un caso de Fibrosis pulmonar idiopática, está patología se define como una enfermedad pulmonar intersticial difusa que afecta el correcto funcionamiento de los pulmones sin ninguna causa en específico. La fibrosis pulmonar idiopática en varios de los casos es asociada con un mal pronóstico que muchas veces puede poner en riesgo la vida del paciente por esta razón es vital importancia conocer los síntomas que se pueden presentar en la enfermedad en conjunto con los signos radiológicos y tomográficos que se puedan observar y ayuden a el control y manejo de la enfermedad. Se presenta el caso de una paciente de sexo femenino de 57 años de edad, sin antecedentes patológicos ni hábitos tóxicos, que acude al centro de salud por presencia de tos, dificultad para respirar y expectoración de color amarillenta blanquecina. Es ingresada al centro hospitalario una frecuencia respiratoria de 24 rpm, una frecuencia cardiaca de 110/ 70, frecuencia cardiaca de 22 Imp y una saturación de oxígeno de 94%, una temperatura de 36° y un peso corporal 58kg. Se le realizan una serie de exámenes complementarios donde se logran observar los patrones característicos de la Fibrosis pulmonar idiopática. Como es una enfermedad idiopática, es decir que no se conoce alguna causa en específico es probable que los síntomas aparezcan de forma repentina o que incluso se empeoren. | es_ES |
| dc.format.extent | 39 p. | es_ES |
| dc.language.iso | es | es_ES |
| dc.publisher | Babahoyo: UTB-FCS, 2021 | es_ES |
| dc.rights | Atribución-NoComercial-SinDerivadas 3.0 Ecuador | * |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/ec/ | * |
| dc.subject | Fibrosis | es_ES |
| dc.subject | Idiopática | es_ES |
| dc.subject | Intersticial | es_ES |
| dc.subject | Expectoración | es_ES |
| dc.subject | Difusa | es_ES |
| dc.title | Paciente femenino de 57 años con fibrosis pulmonar idiopática. | es_ES |
| dc.type | bachelorThesis | es_ES |
Ficheros en el ítem
Este ítem aparece en la(s) siguiente(s) colección(ones)
Excepto si se señala otra cosa, la licencia del ítem se describe como Atribución-NoComercial-SinDerivadas 3.0 Ecuador