Buchanan G R, Scher C S, Button L N, Nathan D G
Pediatrics. 1977 Jan;59(1):45-54.
Twenty-one children with chronic thrombocytopenia of obscure etiology, 19 of whom had normal numbers of bone marrow megakaryocytes, were evaluated in order to determine if factors extrinsic to the platelets themselves (presumably antibodies) caused the thrombocytopenia. The rapid destruction of platelets by such antibodies has been demonstrated to cause idiopathic thrombocytopenic purpura (ITP). History, physical examination, and routine laboratory studies were unable to provide an exact diagnosis in these patients. Measurement of platelet survival, using sodium chromate Cr 51 labeled homologous platelets obtained from unrelated donors, permitted a clear separation of these children into two groups. One group (11 patients) had a markedly shortened platelet life span, and was considered to have chronic ITP. The other group (10 patients) had a normal or only slightly reduced platelet life span. Thus, the destruction of platelets by extrinsic factors could be ruled out. Since the diagnosis of chronic ITP was excluded, splenectomy could be avoided in these patients since it is rarely useful in children with nonimmune forms of chronic thrombocytopenia. Homologous platelet survival measurement is a useful diagnostic tool in certain children with chronic thrombocytopenia.
对21名病因不明的慢性血小板减少症患儿进行了评估,其中19名患儿骨髓巨核细胞数量正常,目的是确定血小板自身以外的因素(可能是抗体)是否导致了血小板减少。业已证明,此类抗体对血小板的快速破坏会导致特发性血小板减少性紫癜(ITP)。病史、体格检查及常规实验室检查均无法对这些患儿做出确切诊断。通过使用从无关供体获取的经铬51酸钠标记的同源血小板来测量血小板存活期,可将这些患儿明确分为两组。一组(11名患儿)血小板寿命明显缩短,被认为患有慢性ITP。另一组(10名患儿)血小板寿命正常或仅略有缩短。因此,可以排除外在因素对血小板的破坏。由于排除了慢性ITP的诊断,这些患儿可避免行脾切除术,因为脾切除术对非免疫性慢性血小板减少症患儿很少有用。同源血小板存活期测量是某些慢性血小板减少症患儿有用的诊断工具。