Hello, Professor Kong's prescription for interstitial pneumonia can treat symptoms: dyspnea and dry cough. Since then, it is often induced and aggravated by colds and acute respiratory infections, and it is gradually aggravated. Gradually, breathing increased, but there was no wheezing, irritating cough or expectoration. A few people had fever, hemoptysis or chest pain. After strenuous exercise, symptoms such as asthma, palpitation, sweating, general fatigue, weight loss, cyanosis of labia and clubbed fingers (toes) appear. Wet rales can be heard in the lung field during physical examination. When complicated with cor pulmonale, there are hyperphonia of pulmonary artery, jugular vein dilatation, hepatomegaly and edema of lower limbs. Pathology: Interstitial pneumonia is inflammation of interstitial tissue of lung, which mainly invades bronchial wall and alveolar wall, especially connective tissue around bronchi, interlobular septa and alveolar septa around bronchi, and most of them are necrotic lesions. Interstitial pneumonia, also known as interstitial lung disease, diffuse lung disease and so on. As a disease name, it has only a history of more than ten years. As the name implies, it is interstitial lung disease. Interstitial pneumonia is not a single disease, but a general term of a large class of diseases, about a hundred kinds, and a few of them are known to have definite causes, such as pneumoconiosis, drug-induced pneumonia and radiation pneumonia. However, quite a few reasons are unknown, such as idiopathic pulmonary fibrosis and sarcoidosis. Although interstitial pneumonia is called "pneumonia", it is mainly not microbial infection such as bacteria and viruses. Idiopathic pulmonary fibrosis (IPF) is a disease with unknown causes, which is characterized by diffuse alveolitis and alveolar structural disorder leading to pulmonary interstitial fibrosis. According to the course of disease, it is divided into three types: acute, subacute and chronic. The so-called Hyman-Ritchie syndrome belongs to acute type, but subacute and chronic are more common in clinic. European scholars usually refer to this disease as cryptofibrillar alveolitis (CFA). America is used to IPF. CFA used to be very popular in China, but recently IPF has been used more. The disease is mostly sporadic, with an estimated incidence of 3 ~ 5/65438+ 10,000, accounting for about 65% of all interstitial lung diseases. It is found in all age groups, and the diagnosis is often between 50 and 70 years old, and the ratio of male to female is 1.5 ~ 2: 1. The prognosis is very poor. Even if early cases respond to hormone therapy, the survival time is generally only 5 years. Professor Kong's prescription for interstitial pneumonia is rigorous and meticulous, and its clinical effect is remarkable. After taking it for 20 days, the patient's dyspnea and cough symptoms improved obviously, and gradually improved after taking it for 3-7 months until he recovered.