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Successful Treatment of Catastrophic Antiphospholipid Antibody Syndrome Associated with MALT Lymphoma by Autologous Hematopoietic Stem Cell Transplantation

机译:自体造血干细胞移植成功治疗与MALT淋巴瘤相关的大灾难性抗磷脂抗体综合征

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A 37-year-old woman with extranodal marginal-zone lymphoma was admitted with a fever, hemiplegia, and severe dyspnea after chemotherapy. Catastrophic antiphospholipid antibody syndrome (CAPS) was suspected based on the histopathological confirmation of small-pulmonary vessel occlusion, evidence of the involvement of three organs, and elevated lupus anticoagulant assay results in a short time span. The patient responded to the initial treatment. One month later, the CAPS and lymphoma relapsed, and the patient underwent autologous hematopoietic stem cell transplantation. Complete remission of the lymphoma has been successfully maintained, and the condition of the patient has remained stable for two years with no further evidence of thrombosis.
机译:一名患有结外边缘区淋巴瘤的37岁妇女因化疗后发烧,偏瘫和严重呼吸困难而入院。基于小肺血管闭塞的组织病理学证实,三个器官受累的证据以及短时间内狼疮抗凝测定结果升高,怀疑是灾难性抗磷脂抗体综合征(CAPS)。病人对最初的治疗有反应。一个月后,CAPS和淋巴瘤复发,患者接受了自体造血干细胞移植。已成功维持淋巴瘤的完全缓解,并且患者的状况已稳定两年,没有进一步的血栓形成迹象。

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