Don’t forget Kawasaki.

Kawazaki’s disease, also known as the mucous lymphoma syndrome, was first discovered by a Japanese man, so his name was Kawazaki’s disease, the second most common vascular disease in childhood. It’s a full-body inflammation disease. Mainly caused to medium-sized vascular damage, especially the coronary artery of the heart, can cause coronary aneurysms of the heart, cardiac myocardiasis, reduced myocardial contraction and heart failure. The disease is more common among boys than among girls, most of it occurring in six months – under five years of age; its causes are not clear at present, and studies have shown that its causes are related to immunosuppressive factors, genetic factors, infection factors (especially viral infections). The most basic manifestations are heat greater than five days, which is usually high and anti-infection treatment is ineffective; conjunction with eyes, i.e., red eyes, red eyes with little rabbits; rashes with various shapes; rashes with dry, red mouths, red tongues, red nipples, like Yang May; skins with red and hard ends of hands and feet, which are also swollen and hard, and in these places after two weeks, which are like gloves; muscular skins around their buttocks; corsets around their necks that touch the size of their peanuts, i.e., a swollen ly lymphobe; and a small child who is resty and weeping and who also has a part of his/her joint pain, mainly on his/her knees, ankles, hips and hips, which generally improves on his/her own back, and does not leave after. The main diagnostic criteria for this disease are these clinical manifestations, which are confirmed by a number of supplementary examinations. If our children have these symptoms, they need to go to the hospital in a timely manner, and professional paediatricians are required to assess whether they have the disease. The most basic need is to check blood routines, blood sank and heart ultrasound to see if there is a possibility of Kawasaki disease. If the above-mentioned manifestations are accompanied by high white cells, high C-reacting protein levels, high blood levels, and an ultrasound coronary artery expansion, aneurysm, and arrhythmia, then Kawazaki is ill. The special effects of this disease are immunoglobins, i.e., immunoglobins extracted from blood. This is a liquid that requires an intravenous injection, usually on the basis of the child ‘ s kg of weight, and usually 1kg of body weight 1-2g of immunoglobin. The medicine is a half-day-1 body temperature after the infusion, but only a small proportion of the children have a fever within 72 hours of the infusion, so the infusion takes about three days, and if the infusion is repeated, the doctor will re-evaluate whether the C-ball protein resistance is effective or not; whether the protein is used again or hormonal; hormones are not used as the first drug of choice; and aspirin is needed to reduce the amount of heat at 30-50 mg/kg body temperature stabilization for about three days, because this small plate of blood in the post-disease period is expected to rise, so it will typically take up to eight weeks at a small dose, and may take longer if the plate lasts longer. A follow-up visit to the hospital usually takes two weeks to four weeks to review the blood routine, three months to six months to review the cardiac ultrasound, and if part of the heart reaches the system, the EK map will be reviewed; and the vaccine for the child will be used 11 months after a live vaccine requires a liquid immunoglobin, because a high level of immunoglobin levels in the body may result in vaccine immunization failure.