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Acute interstitial pneumonia

Acute interstitial pneumonia (AIP) is a rare and rapidly developing fulminant lung injury. The onset is rapid (within a few days to weeks), characterized by fever, cough and shortness of breath, followed by respiratory failure, similar to idiopathic ARDS of unknown cause. The average age of onset was 49 years old, and there was no significant gender difference. Routine laboratory tests were nonspecific. The mortality of AIP is very high (> 60%), and most of them die within 1 ~ 2 months.

Symptoms

Acute hydrogen sulfide poisoning

Accelerated atrial escape rhythm

Acute idiopathic pericarditis

Acute tracheobronchia

Accelerated ventricular autonomic rhythm

Hormone resistant asthma

Acute invasive pulmonary aspergillosis

Familial mixed hyperlipidemia

Familial hypercholesterolemia

Acute laryngeal wind

Intermittent dependent torsade de pointe ventricular tachycardia

Acute bronchiolitis

Familial abnormality β Lipoproteinemia

Acute lung abscess

Corrected transposition of great arteries

Acute mediastinitis

Familial apolipoprotein B100 deficiency

Beriberi heart disease

Decompression sickness

Hyperthyroid heart disease

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