Department of Paediatric Haemato-Oncology, Santobono-Pausilipon Children's Hospital, Via Posillipo, 226, 80123 Napoli, Italy.
Ital J Pediatr. 2014 Apr 10;40:36. doi: 10.1186/1824-7288-40-36.
Hypereosinophilia as first clinical presentation has rarely been reported in paediatric acute lymphoblastic leukaemia. It is commonly associated with specific cytogenetic abnormalities. Although eosinophilia is considered a reactive, non-neoplastic epiphenomenon, it adversely affects patient outcomes, both in children and adults. We describe herewith two paediatric patients who had marked eosinophilia at onset of acute lymphoblastic leukaemia. We point out the importance of a correct differential diagnosis in persistent, unexplained peripheral hypereosinophilia. Clinicians should keep in mind that eosinophilia can be part of the overall pattern of acute leukaemia and therefore needs to be properly investigated. We also provide some recommendations for an appropriate approach to hypereosinophilia - related morbidities.
嗜酸性粒细胞增多症作为儿科急性淋巴细胞白血病的首发临床表现较为罕见,常与特定细胞遗传学异常相关。虽然嗜酸性粒细胞增多被认为是一种反应性、非肿瘤性的伴随现象,但它会对儿童和成人患者的结局产生不利影响。在此,我们描述了两名儿科患者,他们在急性淋巴细胞白血病发病时表现出明显的嗜酸性粒细胞增多。我们指出了在持续性、无法解释的外周血嗜酸性粒细胞增多症时,正确鉴别诊断的重要性。临床医生应牢记,嗜酸性粒细胞增多可能是急性白血病整体表现的一部分,因此需要进行适当的检查。我们还为嗜酸性粒细胞增多相关并发症提供了一些适当处理方法的建议。