Polycythemia vera in children?

summary

We all know that newborn babies sometimes have some diseases. For example, we often say that neonatal polycythemia is one of the more common diseases, and the specific causes are various. In most cases, the clinical manifestations after illness are jaundice after birth, nuclear jaundice in severe cases, or aggravation of heart load, not timely treatment, the harm to the newborn is great. Polycythemia vera in children? Now let me tell you something.

Polycythemia vera in children?

First of all, we all know that the so-called neonatal polycythemia and other diseases can be divided into primary and secondary two categories. Generally speaking, the primary is polycythemia vera; Secondary is mainly caused by tissue hypoxia, and different causes of symptoms are different.

For most babies, the initial symptoms after this neonatal polycythemia are not obvious. When the venous hematocrit of the newborn within one week of birth is ≥ 65%, the peripheral hematocrit is ≥ 70% or the hemoglobin is > 220g / L, the diagnosis of polycythemia can be made.

At present, there are more infants with this disease, and there are certain degrees of severity, mild symptoms are easy to be ignored by patients. When the baby has shortness of breath, continuous fetal circulation and heart failure, loss of appetite and vomiting can not be taken lightly, must check early, early treatment can promote the early recovery of the baby.

matters needing attention

In short, the harm of this disease is multifaceted, due to the increase of blood viscosity, blood stasis, blood volume increase, at this time, not timely treatment may also cause multiple organ dysfunction. Usually we must pay attention to observation, if the red blood cells have reached the standard of polycythemia, early choice of formal treatment is the most critical.