Clare N, Elson D, Manhoff L
Am J Clin Pathol. 1982 Jun;77(6):762-6. doi: 10.1093/ajcp/77.6.762.
Chromosome analysis with giemsa-trypsin banding was performed on circulating myeloblasts and cultured bone marrow fibroblasts from a patient with acute myelofibrosis. Major karyotypic abnormalities were found in the myeloblasts involving chromosomes #1, 3, 5, 13, and 16; no chromosome abnormalities were detected in the fibroblasts. In addition, a pericentric inversion of number 7 was present in the circulating blasts but not the fibroblasts. Pericentric inversions have not previously been associated with acquired abnormalities of malignant cells. These findings support the concept that acute myelofibrosis is a primary malignancy of hematopoietic cells associated with secondary marrow fibrosis. The entity of acute myelofibrosis is discussed and the results of cytogenetic studies of previous reports are reviewed.
对一名急性骨髓纤维化患者的循环成髓细胞和培养的骨髓成纤维细胞进行了吉姆萨 - 胰蛋白酶显带染色体分析。在成髓细胞中发现了涉及1号、3号、5号、13号和16号染色体的主要核型异常;在成纤维细胞中未检测到染色体异常。此外,循环母细胞中存在7号染色体的臂间倒位,而成纤维细胞中没有。臂间倒位以前未与恶性细胞的后天异常相关联。这些发现支持了急性骨髓纤维化是一种与继发性骨髓纤维化相关的造血细胞原发性恶性肿瘤的概念。本文讨论了急性骨髓纤维化的实体,并回顾了既往报道的细胞遗传学研究结果。