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一名白血病患儿异基因骨髓移植后眶后迟发性复发

Retro-orbital late relapse in a child with leukaemia after allogeneic bone marrow transplantation.

作者信息

Colombini A, Barzaghi A, Castagneto M, Bovo G, Rossi M R, Rovelli A, Uderzo C

机构信息

Department of Paediatric Haematology, Milan University, Italy.

出版信息

Acta Haematol. 1995;94(1):44-7. doi: 10.1159/000203970.

Abstract

Relapse after allogeneic bone marrow transplantation (BMT) usually occurs in the bone marrow and is often associated with a poor prognosis. Isolated extramedullary relapse following BMT is exceedingly rare. We observed an isolated relapse in the left retro-orbital region of a 13-year-old girl, 3 years after BMT performed for acute lymphoblastic leukaemia in third complete remission. Computerized tomography revealed a tumor at the inferomedial part of the orbit infiltrating the maxillary and ethmoid sinuses and nasal cavities and also involving the rectus muscles. Histology demonstrated a monomorphic leukaemia infiltrate. Complete disappearance of the retro-orbital mass was obtained with chemotherapy and local irradiation.

摘要

异基因骨髓移植(BMT)后复发通常发生在骨髓,且往往预后不良。BMT后孤立的髓外复发极为罕见。我们观察到一名13岁女孩在急性淋巴细胞白血病第三次完全缓解后接受BMT 3年后,左侧眶后区域出现孤立复发。计算机断层扫描显示眼眶内下部分有一个肿瘤,侵犯上颌窦、筛窦和鼻腔,还累及眼直肌。组织学检查显示为单形性白血病浸润。通过化疗和局部放疗,眶后肿块完全消失。

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