Yoshida Chikamasa, Takeuchi Makoto, Tsuchiyama Junjiro, Sadahira Yoshito
Division of Hematology, Department of Internal Medicine, National Hospital Organization Minami-Okayama Medical Center, Okayama.
Intern Med. 2009;48(22):1973-8. doi: 10.2169/internalmedicine.48.2294. Epub 2009 Nov 16.
We describe a case of systemic mastocytosis associated with myelodysplastic syndrome. The bone marrow showed multifocal clusters of mast cells and myeloid dysplasia. Sequencing of the KIT DNA revealed a point mutation at codon 816 including a substitution of valine for aspartic acid (D816V). The patient's tumor did not respond to imatinib; however, interferon-alpha reduced the bone marrow mast cells and serum total tryptase. The patient remains alive at one year after the diagnosis without disease progression.
我们描述了一例与骨髓增生异常综合征相关的系统性肥大细胞增多症病例。骨髓显示有多灶性肥大细胞簇和髓系发育异常。KIT基因DNA测序显示密码子816处存在点突变,包括天冬氨酸被缬氨酸替代(D816V)。该患者的肿瘤对伊马替尼无反应;然而,α干扰素减少了骨髓肥大细胞和血清总类胰蛋白酶。该患者在诊断后一年仍然存活,且疾病无进展。