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Nowadays, only the spread of idiopathic fibrosing alveolitis is known with certainty. According to statistics, approximately 20 men out of one hundred thousand and 13 women out of the same number suffer from it.

With age, the risk of atenolol pills. Most often it occurs after 60. Mortality is directly proportional to the age category. The older the patients, the higher it is. 3 people per 100 thousand people die from this disease. In turn, the average life expectancy of survivors of this type of pneumonia ranges from 2.5 to 5 years. It should be clarified that about 90% of cases of idiopathic interstitial pneumonia are a disease of idiopathic fibrosing alveolitis. Idiopathic interstitial pneumonia is classified according to the characteristics of the clinical picture, pathomorphological and radiological signs. Pathomonological disorders for each individual form have not yet been identified. All patients experience a decrease in lung volume due to physiological changes as a consequence of the disease. In patients, the results of laboratory tests characteristic of all types of idiopathic diseases are highlighted. Features of clinical and radiological manifestations of idiopathic fibrosing alveolitis.

On radiography, darkening is most often observed in the basal regions. This is the reason for the decrease in the volume of the lower lobes and the formation of honeycomb changes in the lung tissue. The accuracy of diagnosis using an X-ray image is 50%. Features of clinical and radiological manifestations of nonspecific interstitial pneumonia. This disease develops very smoothly. Often people consult a doctor 1.5-3 years after experiencing the first symptoms. Shortness of breath and cough are not very pronounced and increase at a slow pace. Temperature and changes in the nail plates appear no more often than in 10% of cases. The disease is highly treatable.

With this type of pneumonia, pathological changes occur in the alveolar ducts and alveoli in combination with polypoid bronchiolitis. The symptoms are similar to buy atenolol online. The cough may be productive and produce clear sputum. Wheezing can be heard. The shape of the nail phalanges never changes. In addition, a blood test also takes part in the diagnosis. HSC therapy leads to complete recovery of the patient. During X-ray examination, unilateral darkening in the form of nodular shadows is most often visible. The lung area may decrease by up to 25%.

Features of clinical and radiological manifestations of cryptogenic organizing pneumonia. Computed tomography shows subpleural and peribronchial consolidations in the lower lobes of the lungs. Features of clinical and radiological manifestations of acute interstitial pneumonia. With this type of disease, after symptoms of a viral infection, shortness of breath quickly develops. Later cyanosis develops. Over time, the patient requires artificial ventilation. The mortality rate exceeds 50%.

Features of clinical and radiological manifestations of desquamative interstitial pneumonia. Most often, the disease occurs in smokers and is characterized by a dry cough and increasing shortness of breath. Features of clinical and radiological manifestations of lymphoid intertial pneumonia. Symptoms of the disease include weight loss, fever, arthralgia, and sometimes anemia.

In modern medicine, a complete diagnosis can only be made using a surgical lung biopsy. For different types of idiopathic intertial pneumonia, both open and video-assisted thoraxoscopic biopsy can be used. A complete diagnosis of this group of diseases allows one to buy tenormin online not only death from the disease itself, but also the consequences of improper treatment with difficult-to-tolerate drugs that are used due to the complexity of the disease. Nonspecific interstitial pneumonia occurs. Idiopathic interstitial pneumonia. How do idiopathic and other forms of the disease develop?

Idiopathic interstitial pneumonia is an interstitial lung disease of unknown etiology that shares similar clinical features. They are classified into 6 histological subtypes and they are characterized by varying degrees of inflammatory response and fibrosis and are accompanied by dyspnea and typical radiographic changes. The diagnosis is made by analyzing the history, physical examination, radiological studies, pulmonary function tests and lung biopsy. J84 Other interstitial pulmonary diseases.

Known causes of IPD must be excluded. In all cases, the rechest x-ray, pulmonary function tests and high-resolution CT (HRCT). The latter makes it possible to differentiate lesions of the hollow spaces from those of tenormin pills, provide a more accurate assessment of the extent and location of the lesion, and are more likely to detect underlying or concomitant disease (eg, occult mediastinal lymphadenopathy, malignancies, and emphysema). HRCT is best performed with the patient in the prone position to reduce atelectasis of the lower lung.