「Anemia in the tropics」の版間の差分
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*malaria does not cause IDA directly; destruction of RBCs by ''Plasmodium'' does not cause iron loss | *malaria does not cause IDA directly; destruction of RBCs by ''Plasmodium'' does not cause iron loss | ||
**anemia by malaria is mainly by inflammation, which suppresses iron absorption | **anemia by malaria is mainly by inflammation, which suppresses iron absorption | ||
+ | |||
+ | ==sickle cell anemia== | ||
+ | *monogenetic recessive disorder | ||
+ | *hemoglobin mutation | ||
+ | *HbA mutated into HbS (sickle cell trait) or HbC (West Africa) | ||
+ | *sickle cell trait protect against death from severe malaria | ||
+ | **not prevent infection itself | ||
+ | |||
+ | ===clinical picture of SCD=== | ||
+ | *affects all organ systems | ||
+ | *disease pattern and severity varies very much on patients | ||
+ | |||
+ | ===chronic management=== | ||
+ | *first to identify high risk groups | ||
+ | |||
+ | ==thalassemia== | ||
+ | *decreased hemoglobin production | ||
+ | **sickle cell trait is problem of hemoglobin destruction | ||
+ | *beta thalassemia affects beta chain of hemoglobin | ||
+ | *alpha thalassemia affects alpha chain of hemoglobin | ||
+ | *major, media, minor |
2021年5月6日 (木) 16:01時点における版
目次
reference value/cut-off of Hb
- adjust according to altitude of living
diagnosis
- POC test kit: HemoCue
- ferritin increases in inflammation in order to deliver more iron stimulated by inflammation itself as well as to avoid pathogens try to consume iron
- serum transferrin (TIBC) increases in IDA, decreases in inflammation
- zinc protoporphyrin (Zpp)
- soluble transferrin receptor (sTfr)
cause
- malaria does not cause IDA directly; destruction of RBCs by Plasmodium does not cause iron loss
- anemia by malaria is mainly by inflammation, which suppresses iron absorption
sickle cell anemia
- monogenetic recessive disorder
- hemoglobin mutation
- HbA mutated into HbS (sickle cell trait) or HbC (West Africa)
- sickle cell trait protect against death from severe malaria
- not prevent infection itself
clinical picture of SCD
- affects all organ systems
- disease pattern and severity varies very much on patients
chronic management
- first to identify high risk groups
thalassemia
- decreased hemoglobin production
- sickle cell trait is problem of hemoglobin destruction
- beta thalassemia affects beta chain of hemoglobin
- alpha thalassemia affects alpha chain of hemoglobin
- major, media, minor