Describe childhood acute lymphocytic leukemia (ALL) and G6PD deficiency and the incidence, pathophysiology, clinical manifestations, evaluation, and treatment of each
Childhood Acute Lymphocytic leukemia:
ALL is a type of cancer whereby the bonemarrow is develop immature lymphocytes.
Incidence:
Almost 60% of cases are found in children between 0 to 14 years of age.
Pathophysiology:
The bone marrow develops immature lymphoid stem cell which is responsible for making B-cells, T-cells, and Nature killer cells. These immature cells are unable to fight infection. Thus there are more susceptible to get an infection, anemia, and other disorders.
Clinical manifestations:
Treatment:
Chemotherapy, immunotherapy, and radiation therapy are used to treat diseases.
Stem cell replacement therapy to develop new mature cells.
Evaluation:
The child is evaluated based on the progress of the disease, alleviation of signs and symptoms, and response to the treatment.
G6PD deficiency
G6PD is a genetic disorder where the red blood cells are broken down and cause anemia. The G6PD deficiency occurs due to illness, pain medications, antibiotics, intake of naphthalene balls.
Incidence:
It mostly transmits through genetic inheritance and commonly seen in males than females.
Pathophysiology:
Exposure to certain triggers results in a defect of the enzyme Glucose 6 phosphate dehydrogenase. So the red blood cells are destroyed faster resulting in hemolytic anemia.
Clinical manifestations:
Treatment:
Evaluation:
The child is evaluated by the G6PD activity, red blood cell count, temperature, and jaundice level. A diagnostic test helps to analyze patient improvement and treatment response.
Describe childhood acute lymphocytic leukemia (ALL) and G6PD deficiency and the incidence, pathophysiology, clinical man...
Describe childhood acute lymphocytic leukemia (ALL) and G6PD deficiency and the incidence, pathophysiology, clinical manifestations, evaluation, and treatment of each.
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