Katsanis E, Luke K H, Hsu E, Yates J R
CMAJ. 1987 Jul 1;137(1):39-42.
With the recent immigration of Southeast Asians to Canada, hemoglobin E has become a frequent diagnosis. The clinical and hematologic findings in 42 children (mean age 4.3 years) with hemoglobin E are presented. There were 33 heterozygotes (having hemoglobin E trait), 6 homozygotes (having hemoglobin EE) and 3 double heterozygotes (having hemoglobin E-beta-thalassemia). The heterozygotes had low-normal hemoglobin levels and mean corpuscular volumes; coexisting iron deficiency, present in 62% of these children, resulted in substantially lower hemoglobin levels, very low mean corpuscular volumes and lower than expected levels of hemoglobin E on electrophoresis. The children with hemoglobin EE were only slightly anemic, but those with hemoglobin E-beta-thalassemia had severe anemia and required long-term transfusion therapy. Nutritional factors and parasitic infestations were the main causes of iron depletion, which was common, particularly in children less than 2 years old (87%). Physicians of patients of Southeast Asian origin should be aware of the clinical and hematologic presentation of these hemoglobinopathies.
随着近期东南亚人移民到加拿大,血红蛋白E已成为一种常见的诊断疾病。本文介绍了42名血红蛋白E患儿(平均年龄4.3岁)的临床和血液学表现。其中有33名杂合子(具有血红蛋白E性状)、6名纯合子(具有血红蛋白EE)和3名双重杂合子(具有血红蛋白E-β地中海贫血)。杂合子的血红蛋白水平和平均红细胞体积略低于正常;62%的患儿同时存在缺铁情况,这导致血红蛋白水平大幅降低、平均红细胞体积极低以及电泳时血红蛋白E水平低于预期。血红蛋白EE患儿仅有轻度贫血,但血红蛋白E-β地中海贫血患儿有严重贫血,需要长期输血治疗。营养因素和寄生虫感染是铁缺乏的主要原因,铁缺乏情况很常见,尤其是在2岁以下的儿童中(87%)。东南亚裔患者的医生应了解这些血红蛋白病的临床和血液学表现。