首页> 美国卫生研究院文献>Case Reports in Hematology >Autoimmune Demyelinating Polyneuropathy as a Manifestation of Chronic Graft-versus-Host Disease after Adult Cord Blood Transplantation in a Patient with Chronic Lymphocytic Leukemia
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Autoimmune Demyelinating Polyneuropathy as a Manifestation of Chronic Graft-versus-Host Disease after Adult Cord Blood Transplantation in a Patient with Chronic Lymphocytic Leukemia

机译:自身免疫性脱髓鞘性多发性神经病表现为慢性淋巴细胞白血病患者成人脐带血移植后的慢性移植物抗宿主病

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摘要

Immune mediated demyelinating disease after allogeneic stem cell transplantation is a rare entity with unclear etiology. Acute inflammatory demyelinating polyneuropathy (AIDP) has been reported after related and adult unrelated allogeneic stem cell transplantation but no such case has been reported after unrelated cord blood transplantation. We hereby present the first case of AIDP after double umbilical cord blood transplantation (DUCBT). A 55-year-old man with chronic lymphocytic leukemia (CLL) received a cord blood transplant for relapsed refractory disease with high risk cytogenetics. On day 221, patient presented with skin rash, tingling in both lower extremites, and ascending paralysis that progressed rapidly over the course of 2 days. The workup resulted in a diagnosis of AIDP and administration of intravenous immunoglobulins plus steroids was initiated. Motor and sensory powers were fully recovered and his chronic GVHD was managed for several months with single agent sirolimus.
机译:同种异体干细胞移植后的免疫介导的脱髓鞘疾病是病因尚不清楚的罕见实体。在相关和成人无关的异体干细胞移植后,已有急性炎性脱髓鞘性多发性神经病(AIDP)的报道,但在不相关的脐血移植后,尚无此类病例的报道。我们特此介绍双脐带血移植(DUCBT)后AIDP的第一例。一名55岁的慢性淋巴细胞性白血病(CLL)的男子因复发性难治性疾病伴有高风险的细胞遗传学而接受了脐血移植。在第221天,患者出现皮疹,下肢刺痛和在两天内迅速进展的麻痹。该检查诊断为AIDP,并开始静脉注射免疫球蛋白加类固醇。运动和感觉力完全恢复,他的慢性GVHD用单药西罗莫司治疗了几个月。

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