Farhi D C, Luebbers E L, Rosenthal N S
Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Arch Pathol Lab Med. 1998 Jul;122(7):638-41.
Bone marrow examination is rarely required for the diagnosis of childhood anemia, and its diagnostic utility in this setting is unknown.
Marrow specimens from 25 children aged 11 days to 12 years were reviewed to determine the cause of unexplained anemia.
These samples comprised only 2% of pediatric marrow examinations. Hematocrits ranged from 0.12 to 0.31 (mean 0.23). Marrow findings included erythroid hypoplasia (12 of 25, 48%) and hyperplasia (11 of 25, 44%), dyserythropoiesis (2 cases), ringed sideroblasts (2 cases), lymphocytosis (3 cases), and megaloblastic change (1 case). Final diagnoses were transient erythroblastopenia of childhood (15 cases, 60%); iron deficiency and sideroblastic anemia (2 cases each); and congenital dyserythropoietic anemia, anemia of chronic disease, hereditary spherocytosis, and intra-abdominal hemorrhage (1 case each). In two patients, a definitive diagnosis was never made.
Marrow examination contributed to a specific diagnosis in childhood anemia in 92% of cases; the most common diagnosis in this population was transient erythroblastopenia of childhood.
儿童贫血的诊断很少需要进行骨髓检查,其在这种情况下的诊断效用尚不清楚。
回顾了25例年龄在11天至12岁儿童的骨髓标本,以确定不明原因贫血的病因。
这些样本仅占儿科骨髓检查的2%。血细胞比容范围为0.12至0.31(平均0.23)。骨髓检查结果包括红系发育不全(25例中的12例,48%)和增生(25例中的11例,44%)、红细胞生成异常(2例)、环形铁粒幼细胞(2例)、淋巴细胞增多(3例)和巨幼细胞改变(1例)。最终诊断为儿童暂时性红细胞生成减少症(15例,60%);缺铁性贫血和铁粒幼细胞贫血(各2例);先天性红细胞生成异常性贫血、慢性病贫血、遗传性球形红细胞增多症和腹腔内出血(各1例)。有2例患者最终未明确诊断。
骨髓检查在92%的儿童贫血病例中有助于明确诊断;该人群中最常见的诊断是儿童暂时性红细胞生成减少症。