Mallouh A A, Qudah A
Specialty Medical Services Department, Saudi Aramco Medical Services Organization, Dhahran, Saudi Arabia.
J Pediatr. 1993 Apr;122(4):593-5. doi: 10.1016/s0022-3476(05)83542-5.
Three children with homozygous sickle cell disease, 22 months and 8 and 10 years of age, had clinical and hematologic manifestations of aplastic and splenic sequestration crisis simultaneously. They had an acute drop in hemoglobin level (16, 20, and 45 gm/L), reticulocytopenia (0.1%, 0.6%, and 0.3%), and sudden splenic enlargement. Evidence of recent parvovirus infection was demonstrated.
三名患有纯合子镰状细胞病的儿童，年龄分别为22个月、8岁和10岁，同时出现再生障碍性和脾隔离危象的临床和血液学表现。他们的血红蛋白水平急剧下降（分别为16、20和45克/升），网织红细胞减少（分别为0.1%、0.6%和0.3%），脾脏突然肿大。有证据表明近期感染了细小病毒。
