Putterman C, Safadi R, Zlotogora J, Banura R, Eldor A
Department of Medicine, Hadassah University Hospital-Ein Kerem, Jerusalem, Israel.
Ann Hematol. 1993 Apr;66(4):209-12. doi: 10.1007/BF01703237.
Dyskeratosis congenita is a congenital multisystem disorder, characterized by skin pigmentation, dystrophic nails, and leukoplakia. Hematologic abnormalities progressing to severe pancytopenia play a significant role in the poor prognosis of afflicted patients. We report on a patient with dyskeratosis congenita and severe aplastic anemia, complicated by life threatening infection. The patient was treated with recombinant granulocyte-macrophage colony-stimulating factor. This therapy resulted in a moderate and transient improvement in absolute neutrophil counts. Current concepts regarding the pathogenesis and etiology of dyskeratosis congenita are discussed, while reviewing the available therapeutic options.
先天性角化不良是一种先天性多系统疾病,其特征为皮肤色素沉着、指甲营养不良和黏膜白斑。进展为严重全血细胞减少的血液学异常在患病患者的不良预后中起重要作用。我们报告一例先天性角化不良合并严重再生障碍性贫血并伴有危及生命感染的患者。该患者接受了重组粒细胞-巨噬细胞集落刺激因子治疗。该治疗使绝对中性粒细胞计数有中度且短暂的改善。在回顾现有治疗选择的同时,讨论了关于先天性角化不良发病机制和病因的当前概念。