Interstitial pneumonia in children is often combined with congenital pathology, such as reirofibromatosis and Marfan syndrome.
With prematurity and a baby weighing less than 1500 grams, the chance of survival is no more than 30%.
Acute interstitial pneumonia.

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It is essentially a respiratory distress syndrome that occurs suddenly in apparently healthy people over 40 years of age. In the septa there are inflammatory changes, proliferation of fibroblasts, thickening of the walls of the alveoli, atypical pneumocytes. The airways collapse, hypoxia develops with respiratory failure. The onset is sudden, with fever, cough and shortness of breath.

It is difficult to buy omeprazole online from other inflammatory lung diseases, since the changes are morphological in nature, and the diagnosis can be definitively confirmed by histopathology.logical examination of lung biopsy. The radiograph is characterized by diffuse bilateral darkening of the lung fields.

Treatment boils down to maintaining impaired respiratory function using artificial ventilation and oxygen therapy. Attempts to use omeprazole pills glucocorticoid hormones did not produce reliable positive results. The prognosis is serious, but not hopeless. 60% of patients die in the first six months from increasing respiratory failure. Those who survive the first attack have a chance of a full recovery. Cryptogenic organizing pneumonia.

People of the same age group are susceptible. Moreover, cryptogenic organizing pneumonia does not depend on the fact of smoking. The essence of the disease is that actively developing granulations block the lumen of the alveoli, causing inflammation in the neighboring alveoli. Every fifth patient has bronchial obstruction. The blood test showed nonspecific leukocytosis, accelerated ESR.

Biopsy confirms granulation proliferation and areas of organizing pneumonia. These changes can be secondary in nature and determined against the background of any other interstitial pathology. Treatment of organizing pneumonia consists of corticosteroid hormones. The prognosis is favorable - usually the patient recovers after 2 weeks. The situation is somewhat more serious with linear darkening and increased pulmonary pattern.

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Desquamative interstitial pneumonia. The disease has a direct connection with inhalation of cigarette smoke in the past or present. Chronic pneumonia develops with mononuclear cells infiltrating the airways of the lungs. Lung desquamation means desquamation. Where does it happen? It turned out that macrophage cells, which are located in the terminal sections of the bronchi, were mistakenly taken for desquamated pneumocytes. The walls of the alveoli are represented by swollen pneumocytes, the interstitium is infiltrated with lymphocytes, plasma cells, and rarely eosinophils.

Desquamative pneumonia is the most favorable in terms of treatment. It is enough to buy prilosec online smoking and the chance of recovery increases to 75%. Sometimes a course of corticosteroids and cytostatics is necessary. Idiopathic pulmonary fibrosis. This is a common form that is characterized by progressive fibrosis. People of both sexes over the age of 50 get sick. There is a clear connection with smoking. There is a role of genetic predisposition in the development of the disease. A combination of different factors reprograms the cells lining the alveoli, resulting in fibroblast proliferation.

The disease develops gradually, increasing shortness of breath, non-productive cough, wheezing when inhaling, reminiscent of omeprazole pills of cellophane. The progression of the disease lasts from 3 months to 3 years, after which death occurs from respiratory failure. Lung cancer occurs more often than usual in these patients. One of the signs of idiopathic pulmonary fibrosis is a change in the terminal phalanges of the fingers - they take on the appearance of drumsticks.

Treatment does not offer much prospects for recovery. Therapy is aimed at maintaining respiratory function. Oxygen therapy is recommended. Some countries use the drug Pirfenidone - it inhibits the development of fibrous tissue. Lung transplantation is performed provided there are no other changes in the body. There are age restrictions - no older than 65 years. Lymphoid interstitial pneumonia.

This form is more common in women and girls. It is assumed that the cause of its occurrence is an autoimmune process or the body’s reaction to the introduction of a virus.

Often such patients are diagnosed with the Epstein-Bar virus, and there is also a connection with HIV infection. With lymphoid interstitial pneumonia, primary damage to the interalveolar septa and alveoli occurs due to infiltration by lymphocytes and plasma cells.
The average age of patients is 54 years. The main complaints are cough and shortness of breath, gradually increasing over several months or years. On auscultation, moist rales are heard.
Such patients often have concomitant systemic diseases. systemic lupus erythematosus, rheumatoid arthritis, Hoshimoto's thyroiditis.
X-ray changes are nonspecific, as are the CT findings. A lung biopsy more accurately confirms the diagnosis.
Lymphoid interstitial pneumonia is treated with glucocorticoids, either alone or in combination with cytotoxic drugs. The prognosis is very variable - spontaneous recovery may occur, fibrosis may develop with increasing respiratory failure.

Blood tests in almost all patients reveal low rises in temperature, gammopathy and a decrease in gamma globulins. Lymphoid interstitial pneumonia gives a chance of five-year survival to slightly more than half of those affected. Nonspecific interstitial pneumonia. A feature of this nonspecific pneumonia is the high incidence of incidence in young women without any connection with smoking. Average age is 40–45 years. Nonspecific interstitial pneumonia is similar in clinical coursewith idiopathic pulmonary fibrosis. The main complaints are cough and chronic, increasing shortness of breath. Low rises in temperature and malaise may be observed.