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Plasma exchange and continuous hemodiafiltration as an initial treatment for diffuse large B-cell lymphoma-associated hemophagocytic syndrome

机译:血浆置换和持续血液透析滤过作为弥漫性大B细胞淋巴瘤相关的噬血细胞综合征的初始治疗

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A 68-year-old man was admitted to our hospital because of fever, jaundice and hepatosplenomegaly. A diagnosis of diffuse large cell, B-cell type malignant lymphoma, associated with hemophagocytic syndrome (LAHS), was made. CT scan revealed lymphadenopathy in the abdominal cavity and multiple tumors in the spleen. Performance status and hepatic coma grade were 4 and II, respectively. Laboratory findings showed bicytopenia (Hb 9.9 g/dl, platelet 35 x 10(3)/microliter), severe liver dysfunction (ALP 1,115 U/l, gamma-GTP 437 U/l, T.Bil 15.4 mg/dl, D.Bil 12.8 mg/dl) and elevated levels of beta 2 microglobulin (12.9 mg/dl), ferritin (2,300 ng/ml) and sIL-2 receptor (36,900 U/ml). Plasma exchange (PE) and continuous hemodiafiltration (CHDF) enabled the patient to undergo diagnostic procedures, irradiation (total 34 Gy) and chemotherapy. Biopsy specimens revealed infiltration of lymphoma cells into the liver and bone marrow. We measured the blood concentrations of TNF-alpha, IL-6, and IL-8 before and after PE and CHDF by the ELISA method, and found normalization of hypercytokinemia after the procedure. It was suggested that initial treatment with PE and CHDF was effective for control of HPS, enabling us to perform chemotherapy for the lymphoma.
机译:一名68岁的男子因发烧,黄疸和肝脾肿大入院。诊断为弥漫性大细胞,B细胞型恶性淋巴瘤,并伴有噬血细胞综合征(LAHS)。 CT扫描显示腹腔有淋巴结肿大,脾脏有多个肿瘤。表现状态和肝昏迷等级分别为4和II。实验室检查结果显示双血细胞减少症(Hb 9.9 g / dl,血小板35 x 10(3)/微升),严重肝功能障碍(ALP 1,115 U / l,γ-GTP437 U / l,T.Bil 15.4 mg / dl,D.比尔12.8 mg / dl)和升高水平的β2微球蛋白(12.9 mg / dl),铁蛋白(2,300 ng / ml)和sIL-2受体(36,900 U / ml)。血浆置换(PE)和连续血液透析滤过(CHDF)使患者能够进行诊断程序,放射线(总计34 Gy)和化疗。活检标本显示淋巴瘤细胞浸润到肝脏和骨髓中。我们通过ELISA方法测量了PE和CHDF之前和之后的TNF-α,IL-6和IL-8的血药浓度,并在手术后发现了高细胞血症的正常化。有人提出,用PE和CHDF进行初始治疗可有效控制HPS,从而使我们能够对淋巴瘤进行化学疗法。

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