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Evaluación clínico-radiológica y clasificación de la bronquiolitis del adulto / Bronchiolar disorders: clinical-radiological assessment and classification
Saldías P, Fernando; Díaz P, Orlando; González B, Sergio; Osses A, Rodrigo.
  • Saldías P, Fernando; Pontificia Universidad Católica de Chile. Facultad de Medicina. Departamento de Enfermedades Respiratorias. Santiago. CL
  • Díaz P, Orlando; Pontificia Universidad Católica de Chile. Facultad de Medicina. Departamento de Enfermedades Respiratorias. Santiago. CL
  • González B, Sergio; Pontificia Universidad Católica de Chile. Facultad de Medicina. Departamento de Anatomía Patológica. Santiago. CL
  • Osses A, Rodrigo; Hospital de Los Ángeles. Servicio de Medicina. CL
Rev. méd. Chile ; 139(9): 1218-1228, set. 2011. ilus, tab
Article in Spanish | LILACS | ID: lil-612249
ABSTRACT
Bronchiolar disorders are generally difficult to diagnose. A detailed clinical history may point toward a specific diagnosis. Pertinent clinical questions include history of smoking, collagen vascular disease, inhalation injury, medication use and organ transplantation. It is important also to evaluate possible systemic and pulmonary signs of infection, evidence of air trapping, and high-pitched expiratory wheezing, which may suggest small airways involvement. Pulmonary function tests and plain chest radiography may demonstrate abnormalities; however, they rarely prove sufficiently specific to obviate bronchoscopic or surgical biopsy. High-resolution CT (HRCT) scanning of the chest is often an important diagnostic tool to guide diagnosis in these difficult cases, because different subtypes of bronchiolar disorders may present with characteristic image findings. Some histopathologic patterns of bronchiolar disease may be relatively unique to a specific clinical context but others are nonspecific with respect to either etiology or pathogenesis. Primary bronchiolar disorders include acute bronchiolitis, respiratory bronchiolitis, follicular bronchiolitis, mineral dust airway disease, constrictive bronchiolitis, diffuse panbronchiolitis, and other rare variants. Prominent bronchiolar involvement may be seen in several interstitial lung diseases, including hypersensitivity pneumonitis, collagen vascular disease, respiratory bronchiolitis-associated interstitial lung disease, cryptogenic organizing pneumonia, and pulmonary Langerhans’ cell histiocytosis. Large airway diseases that commonly involve bronchioles include bronchiectasis, asthma, and chronic obstructive pulmonary disease. The clinical and prognostic significance of a bronchiolar lesion is best determined by identifying the etiology, underlying histopathologic pattern and assessing the correlative clinic-physiologic-radiologic context.
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Full text: Available Index: LILACS (Americas) Main subject: Bronchiolitis Type of study: Diagnostic study / Prognostic study Limits: Humans Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2011 Type: Article Affiliation country: Chile Institution/Affiliation country: Hospital de Los Ángeles/CL / Pontificia Universidad Católica de Chile/CL

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Full text: Available Index: LILACS (Americas) Main subject: Bronchiolitis Type of study: Diagnostic study / Prognostic study Limits: Humans Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2011 Type: Article Affiliation country: Chile Institution/Affiliation country: Hospital de Los Ángeles/CL / Pontificia Universidad Católica de Chile/CL