Zeiser R, Grüllich C, Bertz H, Pantazis G, Hufert F T, Bley T A, Finke J
Department of Hematology/Oncology, Medical Center, University of Freiburg, Hugstetterstrasse 55, Freiburg 79106, Germany.
Bone Marrow Transplant. 2004 Jan;33(2):243-5. doi: 10.1038/sj.bmt.1704311.
A 55-year-old man with acute myeloid leukemia in second relapse presented 4 months after haploidentical CD34+-selected hematopoietic stem cell transplantation (HSCT) with symmetric, progressive neurological deficits of the lower extremities. Although there was no molecular evidence for drug resistance in the cerebral-spinal fluid, antiviral combination therapy failed to control the rapidly progressing CMV polyradiculopathy (PRP) and encephalitis, which were confirmed by autopsy studies. Late CMV PRP as an unusual manifestation of CMV disease should be kept in mind in patients with suggestive neurological symptoms after HSCT.
一名55岁急性髓系白血病二次复发的男性患者,在单倍体相合CD34+选择的造血干细胞移植(HSCT)4个月后出现双下肢对称性、进行性神经功能缺损。尽管脑脊液中没有耐药的分子证据,但抗病毒联合治疗未能控制快速进展的巨细胞病毒多神经根病(PRP)和脑炎,尸检研究证实了这一点。HSCT后出现提示性神经症状的患者应牢记迟发性巨细胞病毒PRP是巨细胞病毒疾病的一种不寻常表现。