[侵犯纵隔的粒细胞肉瘤]。

Archives francaises de pediatrie Pub Date : 1993-11-01
M Ouchiha, A Ferster, P Heiman, W Bujan, N Perlmutter, C Devalck, E Sariban
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引用次数: 0

摘要

背景:粒细胞肉瘤多见于成人;它可以是急性非淋巴细胞白血病的肿瘤定位。本报告描述了一例婴幼儿急性髓性白血病。病例报告:一名14个月大的女婴因双侧颈部淋巴结肿大而入院。在过去的一个月里,它们的数量增加了,并伴有发烧和厌食。肝、脾中度肿大。血液学数据:Hb = 7.5 g%;白细胞= 14,900/mm3;血小板= 614000 /mm3。未见异常细胞。x光和核磁共振显示纵隔肿块。骨显像显示正常,但骨髓造影显示一些非典型细胞,在颈部淋巴结活检中也可见。电镜检查显示这些细胞起源于髓系。免疫组织化学证实了这一点。细胞遗传学检查显示淋巴结和骨髓图中有许多染色体异常。经过9个月的化疗,这个孩子现在已经康复。结论:儿童急性髓母细胞白血病表现为粒细胞性肉瘤,无明显骨髓浸润,诊断困难。临床表现为纵隔肿块是罕见的。细胞遗传学研究是诊断的决定性因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Granulocytic sarcoma with mediastinal involvement].

Background: Granulocytic sarcoma is more frequent in adults; it can be a tumoral localization of acute non-lymphoblastic leukemia. This report describes an infantile case revealing an acute myeloid leukemia.

Case report: A 14 month-old girl was admitted because of enlarged bilateral cervical lymph nodes. They had increased in volume over the past month and were accompanied by fever and anorexia. The liver and spleen were moderately enlarged. Hematologic data were: Hb = 7.5 g%; leucocytes = 14,900/mm3; platelets = 614,000/mm3. There were no abnormal cells. X-rays and MRI showed a mediastinal mass. Bone scintigraphy was normal but the myelogram showed a few atypical cells that were also seen in a biopsy of the cervical lymph node. Electron microscopic examination of these cells showed that they were myeloid in origin. This was confirmed by immunohistochemistry. The cytogenetic examination showed many chromosomal abnormalities in the lymph node and myelogram. The child is now recovered after nine months of chemotherapy.

Conclusion: Diagnosis of acute myeloblastic leukemia in children is difficult when it is revealed by granulocytic sarcoma without major infiltration of bone marrow. The clinical presentation as a mediastinal mass is rare. The cytogenetic study was determinant for diagnosis.

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