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首页> 外文期刊>DMW: Deutsche Medizinische Wochenschrift >Treatment and course of a man with systemic sclerosis before and after hematopoetic blood stem cell transplantation [Therapie und Verlauf bei einem Patienten mit systemischer Sklerose vor und nach Blutstammzelltransplantation]
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Treatment and course of a man with systemic sclerosis before and after hematopoetic blood stem cell transplantation [Therapie und Verlauf bei einem Patienten mit systemischer Sklerose vor und nach Blutstammzelltransplantation]

机译:造血干细胞移植前后全身性硬化症患者的治疗和过程[血液干细胞移植前后全身性硬化症患者的治疗和过程]

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History and admission findings: A 66-year-old patient presented in our clinic with increasing painful swelling of his hands, whole body stiffness, weight loss and dyspnoea upon exercise. Examinations: The physical examination revealed a marked skin sclerosis of hands, extremities and the face. Fist closure was impossible. Pulmonary CT scan showed lung fibrosis and ground glass opacities. Antinuclear antibodies and antibodies against Scl70 were positive. CRP, LDH, NT-Pro-BNP were elevated. Diagnosis, treatment and course: A diffuse cutaneous systemic sclerosis with an active interstitial pneumonia and lung fibrosis was diagnosed. Three pulses of cyclophosphamide 1.4 g every three weeks were ineffective to halt the progression of skin sclerosis, joint contractures and decline of pulmonary function. Mobilisation chemotherapy was initialized and blood stem cells were harvested. Blood stem cells were reinfused after myeloablative chemotherapy with melphalan. A maintainance therapy with mycophenolic acid was initiated after recovery of hematopoiesis. Six months after blood stem cell transplantation a decrease of skin sclerosis and an increasing recovery of joint mobility and physical strength was observed. Conclusion: Patients with a progressive systemic sclerosis and further risk factors should be treated with high-dose chemotherapy with blood stem cell transplantation before organ function is severely compromised. In cases with contraindications against cyclophosphamide or anti-thymocyte-globulin melphalan can be discussed as an alternative.
机译:病史和入院发现:一位66岁的患者在我们的诊所就诊,他的手部疼痛肿胀,全身僵硬,体重减轻和运动后呼吸困难加剧。检查:身体检查显示手,四肢和面部皮肤明显硬化。拳头闭合是不可能的。肺部CT扫描显示肺纤维化和玻璃液混浊。抗核抗体和抗Scl70抗体均为阳性。 CRP,LDH,NT-Pro-BNP升高。诊断,治疗和过程:诊断为弥漫性皮肤系统性硬化症,伴活动性间质性肺炎和肺纤维化。每三周三脉冲1.4 g的环磷酰胺不能有效阻止皮肤硬化,关节挛缩和肺功能下降。开始动员化学疗法并收集血液干细胞。骨髓消融化疗后用美法仑重新注入血液干细胞。造血功能恢复后,开始使用霉酚酸进行维持治疗。血液干细胞移植后六个月,皮肤硬化症减少,关节活动度和体力恢复增加。结论:患有进行性系统性硬化症和其他危险因素的患者,应在器官功能严重受损之前接受大剂量化疗加血干细胞移植治疗。在对环磷酰胺或抗胸腺细胞球蛋白有禁忌症的情况下,可以选择美法仑。

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