Takano T, Zielenska M, Becker L E
Department of Pathology, Hospital for Sick Children, Toronto, Ontario, Canada.
Neuropediatrics. 1998 Jun;29(3):151-4. doi: 10.1055/s-2007-973552.
Cytomegalovirus (CMV) encephalitis is exceptional in patients with genetically determined immune deficiency syndromes. Neuropathologic findings of CMV encephalitis were present at postmortem examination in a child we treated for severe combined immune deficiency. Cultured skin fibroblasts of this male infant revealed a deficiency of adenosine deaminase (ADA). Lacking a suitable bone marrow donor, we used transfusions of red blood cells as a source of ADA. However, the child developed encephalopathy and died at 16 months. The main neuropathologic findings were numerous, widely distributed inclusion-bearing and CMV antigen-positive cells; a complete lack of inflammatory reaction; and cell-to-cell fusion of infected cells reflecting the child's severely impaired immune response.
巨细胞病毒(CMV)脑炎在患有基因决定的免疫缺陷综合征的患者中较为罕见。我们治疗的一名患有严重联合免疫缺陷的儿童在尸检时发现了CMV脑炎的神经病理学表现。该男婴培养的皮肤成纤维细胞显示腺苷脱氨酶(ADA)缺乏。由于缺乏合适的骨髓供体,我们使用红细胞输血作为ADA的来源。然而,该儿童出现脑病并于16个月时死亡。主要神经病理学表现为大量广泛分布的含包涵体和CMV抗原阳性细胞;完全缺乏炎症反应;以及受感染细胞的细胞间融合,反映出该儿童严重受损的免疫反应。