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儿童系统性红斑狼疮合并急性淋巴细胞白血病。

Acute lymphoblastic leukaemia in a child with systemic lupus erythematosus.

机构信息

Pediatric Haematology Division, Hacettepe Medical Faculty, Ankara, Turkey.

出版信息

Lupus. 2012 Jul;21(8):910-3. doi: 10.1177/0961203312436859. Epub 2012 Feb 13.

Abstract

Haematological involvement of systemic lupus erythematosus (SLE) - which ranges from the well-described haemolytic anaemia to macrophage activation syndrome - has a large impact on both morbidity and mortality. On the other hand, association between haematological malignities and SLE - in terms of pathophysiology and molecular genetics - is an obscure entity which has not been clarified evidently to date. Herein, we present a six-year-old female with the diagnosis of SLE who developed acute lymphoblastic leukaemia following a period of myelodysplasia. It could possibly be coincidental; however, persistent cytopenia, prominent dysplasia on bone marrow smears and azathioprine treatment may be considered as possible triggers for the development of leukaemia in the present case.

摘要

系统性红斑狼疮(SLE)的血液学受累范围广泛,从描述明确的溶血性贫血到巨噬细胞活化综合征不等,对发病率和死亡率都有很大影响。另一方面,血液系统恶性肿瘤与 SLE 之间的关联——就病理生理学和分子遗传学而言——是一个尚未明确的实体,迄今为止尚未得到明确阐明。在此,我们介绍了一位 6 岁女性,诊断为 SLE,在骨髓增生异常后发展为急性淋巴细胞白血病。这可能是巧合;然而,持续性细胞减少症、骨髓涂片上明显的发育异常和硫唑嘌呤治疗可能被认为是导致本例白血病发生的可能诱因。

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