Ojala A E, Pääkkö E, Lanning F P, Harila-Saari A H, Lanning B M
Department of Diagnostic Radiology, Oulu University Hospital, Finland.
Clin Radiol. 1998 Feb;53(2):131-6. doi: 10.1016/s0009-9260(98)80060-3.
T1-weighted magnetic resonance imaging (MRI) of the lower extremities was performed 5 years after the cessation of therapy on 25 children treated for acute lymphoblastic leukaemia (ALL). Signal intensity pathologies considered to be related with the leukaemia itself or the treatment of ALL were found in nine of 25 children (36%). Two of these children had findings of osteonecrosis, five had a patchy signal pattern, one had diffuse inhomogeneity of the bone marrow signal intensity in complete remission and one had diffusely decreased signal intensity preceding the diagnosis of relapse. MRI unexpectedly revealed many bone marrow pathologies in symptomless children successfully treated for ALL. Especially, osteonecrosis might cause significant disability, and the aetiology, clinical course and prognosis of this complication are not well known. The intensive dexamethasone medication included in the treatment protocols may be responsible for the development of osteonecrosis. However, the prognosis of osteonecrosis in the long run requires further studies.
在25名接受急性淋巴细胞白血病(ALL)治疗的儿童停止治疗5年后,对其下肢进行了T1加权磁共振成像(MRI)检查。在25名儿童中有9名(36%)发现了被认为与白血病本身或ALL治疗相关的信号强度病变。其中两名儿童有骨坏死表现,五名有斑片状信号模式,一名在完全缓解期骨髓信号强度呈弥漫性不均匀,一名在复发诊断前信号强度弥漫性降低。MRI意外地在成功治疗ALL的无症状儿童中发现了许多骨髓病变。特别是,骨坏死可能导致严重残疾,而这种并发症的病因、临床过程和预后尚不清楚。治疗方案中包含的大剂量地塞米松用药可能是骨坏死发生的原因。然而,骨坏死的长期预后需要进一步研究。