Granel B, Serratrice J, Rey J, David M, Pache X, Bernit E, Swiader L, Disdier P, Weiller P J
Service de médecine interne, hôpital de la Timone, 264, rue Saint-Pierre, 13385 Marseille, France.
Rev Med Interne. 2001 Jul;22(7):664-7. doi: 10.1016/s0248-8663(01)00405-2.
Acute parvovirus B19 infection induces a transient inhibition of erythroid cell formation, which may induce an erythroblastopenia crisis in patients suffering from chronic hemolytic anemia.
We report here an exceptional observation of acute erythroblastopenia crisis with good outcome, occurring at the same time in a mother and her son, both suffering from hereditary spherocytosis. Diagnosis of parvovirus infection is based on detection of serum parvovirus B19-specific immunoglobulin M antibodies in the mother and her son and by the positivity of parvovirus B19 DNA detected by PCR in serum in the mother. Outcome was good, with the end of the erythroblastopenia crisis obtained 7 to 10 days later, but requiring blood transfusion in the mother.
Our observation is a reminder that the contagiosity of parvovirus B19 is high in household contacts and that protection of family members should rapidly be considered in hereditary spherocytosis.
急性B19微小病毒感染会引起红系细胞生成的短暂抑制,这可能在患有慢性溶血性贫血的患者中诱发成红细胞减少危象。
我们在此报告了一例急性成红细胞减少危象的特殊观察病例,结果良好,该病例同时发生在一位母亲及其儿子身上,他们都患有遗传性球形红细胞增多症。微小病毒感染的诊断基于在母亲及其儿子体内检测到血清微小病毒B19特异性免疫球蛋白M抗体,以及母亲血清中通过聚合酶链反应检测到的微小病毒B19 DNA呈阳性。结果良好,7至10天后成红细胞减少危象结束,但母亲需要输血。
我们的观察提醒人们,B19微小病毒在家庭接触者中的传染性很高,对于遗传性球形红细胞增多症患者,应迅速考虑对其家庭成员进行保护。