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Pediatri c nodal marginal zone lymph oma in a Japanese boy

机译:日本男孩小儿节核心边缘区淋巴瘤

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A 13-year-old boy with no remarkable past history presented with a 6 month history of right inguinal lymphadenopathy and a 1 month history of left cervical lymphadenopathy. Physical examination indicated no splenomegaly. Complete blood count was as follows: white blood cell count, 7.0 9 10 9 /L with normal differential; hemoglobin, 14.1 g/dL; and platelet count, 225 9 10 9 /L. Lactate dehydrogenase was 211 U/L, and other components of the comprehensive meta-bolic panel were also normal. On 18 F-uorodeoxyglucose positron emission tomography, uptake was seen in left cervi-cal, right inguinal, and right external iliac lymph nodes (LN; Fig. 1a). There was no evidence of bone marrow inltration.
机译:一个13岁的男孩,没有出现出色的过去的历史,患有6个月的右侧腹股沟淋巴结病和左宫颈淋巴结病的1个月历史。 体格检查表明没有脾肿大。 完全血统如下:白细胞计数,7.0 9 10 9 / L,正常差异; 血红蛋白,14.1g / dl; 和血小板计数,225 9 10 9 / l。 乳酸脱氢酶是211u / l,综合元胸罩的其他组分也正常。 在18 F-uorodoxyglucose正电子发射断层扫描中,在左心核桃,右腹股沟和右外部髂骨淋巴结(LN;图1A)中看到摄取。 没有骨髓中没有证据。

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