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[无菌性骨坏死作为白血病和严重再生障碍性贫血成功治疗后的晚期并发症]

[Aseptic bone necroses as a late complication following successful treatment of leukemias and severe aplastic anemia].

作者信息

Slavc I, Urban C, Schwingshandl J, Ritter G, Trauner R

机构信息

Universitäts-Kinderklinik Graz.

出版信息

Klin Padiatr. 1987 Nov-Dec;199(6):449-52. doi: 10.1055/s-2008-1026838.

Abstract

Aseptic bone necrosis is a well known complication after corticosteroid treatment in adults and several hundred cases have been reported. Alterations in fat metabolism with vascular occlusion due to fat embolization, as well as microtraumata and osteoporosis are discussed as etiologic factors. In contrast, aseptic bone necrosis in relation to corticosteroid treatment is rare in children and adolescents. We therefore report 3 patients, aged from 10 to 18 years, suffering from severe aplastic anemia, meningeal relapse after acute lymphocytic leukemia and acute myelocytic leukemia respectively, who developed aseptic bone necrosis 6, 11, and 20 months following the onset of corticoid therapy. The patients survive from 28+ to 50+ months after diagnosis of their initial hematologic disease, as it can be expected today for increasing numbers of patients. We therefore believe, that aseptic bone necrosis may represent a serious therapy related complication and suggest that, diagnostic examination in patients with suspicious complaints of the hip, shoulder or knee should also exclude the possibility of a bone necrosis after leucemic relapse has been ruled out. Since radiological changes only develop several weeks to months after the onset of the clinical symptoms and because of the disabling consequences for patients, misdiagnosed at the beginning, a 99 technetium bone scan should be done as early as possible. Corticosteroids, despite their serious side effects are still being considered as a important part of hematologic therapy and are not being omitted in the near future, so that the earliest possible diagnosis of bone necrosis will remain of great importance.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

无菌性骨坏死是成人接受皮质类固醇治疗后一种众所周知的并发症,已有数百例报道。脂肪代谢改变伴脂肪栓塞导致血管闭塞,以及微创伤和骨质疏松被认为是病因。相比之下,儿童和青少年中与皮质类固醇治疗相关的无菌性骨坏死较为罕见。因此,我们报告3例年龄在10至18岁之间的患者,分别患有严重再生障碍性贫血、急性淋巴细胞白血病和急性髓细胞白血病脑膜复发,在开始皮质类固醇治疗后6、11和20个月出现无菌性骨坏死。这些患者在诊断出最初的血液系统疾病后存活了28 +至50 +个月,如今越来越多的患者都能做到这一点。因此,我们认为无菌性骨坏死可能是一种严重的治疗相关并发症,并建议在排除白血病复发后,对于髋部、肩部或膝部有可疑症状的患者进行诊断检查时,也应排除骨坏死的可能性。由于放射学改变在临床症状出现数周或数月后才会出现,且由于一开始诊断错误会给患者带来致残后果,应尽早进行锝-99骨扫描。尽管皮质类固醇有严重的副作用,但仍被视为血液学治疗的重要组成部分,近期也不会被摒弃,因此尽早诊断骨坏死仍将非常重要。(摘要截选至250字)

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