A CASE OF VASOOCLUSIVE CRISIS DUE TO SICKLE CELL DISEASE
겸상적혈구 혈중에 의한 동통성 발작 1례
배, 택환; 정, 윤석; 김, 준식; 김, 현수; 김, 효철; 곽, 연식; 조, 준필
Taehan Ŭnggup Ŭihakhoe chi, 6(1):132-136, 1995
Taehan Ŭnggup Ŭihakhoe chi; Journal of the Korean Society of Emergency Medicine; 대한응급의학회지
The sickle cell disease are a group of hemoglobin disorders characterized by red cells that undergo sickle shape transformation when they are deoxygenated. Sickle cell disease is transmitted as an autosomal recessive trait. This unusual property, due to the polymerization of sickle hemoglobin results in anemia and vasoocclusive complication, The most clinical significant of these disease are sickle cell anemia, sickle cell hemoglobin C disease, and sickle cell beta thalassemia. Symptoms of pallor, fever, abdominal and joint pain, enlargement of the liver and spllen, swelling of hands and feet first appear near the latter part of the first year of life. Intravascular sickling affects all organs. For clinical and therapeutic purposes, exacerbations may be classified as vasoocclusive or pain, aplastic, hemolytic or sequestration crisis. We experienced a 22 year old female patient who suffered severe multiple joint pain and back. Pain though to be caused by vase-occlussive phenomena.
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