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首页> 外文期刊>Hepato-gastroenterology. >Intestinal Behcet's disease associated with myelodysplastic syndrome with chromosomal trisomy 8--a report of two cases and a review of the literature.
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Intestinal Behcet's disease associated with myelodysplastic syndrome with chromosomal trisomy 8--a report of two cases and a review of the literature.

机译:伴有骨髓增生异常综合症的肠道白塞氏病伴染色体三体性8型-两例报道并文献复习。

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摘要

Two cases of intestinal Behcet's disease, which developed in the state of myelodysplastic syndrome with trisomy 8, are presented. Both cases are included in the incomplete type of Behcet's disease, with recurrent aphthous stomatitis, skin lesions, genital ulcers or vascular involvement and punched-out ulcers in the cecum, without ocular involvement. The chromosomal analyses revealed chromosomal abnormalities, including trisomy 8, in both cases. Chromosomal trisomy 8 was shown in all 6 cases with the intestinal Behcet's disease associated with myelodysplastic syndrome reported previously, including our patients. Their histories indicated that myelodysplastic syndrome might have started before the development of intestinal Becet's disease. Theses findings suggested that chromosomal trisomy 8 might play an important role in the pathogenesis, at least in some groups, of intestinal Behcet's disease.
机译:介绍了两例在白细胞增生异常综合征伴三体性8的状态下发展的肠道白塞病。两种情况均包括在不完全类型的白塞氏病中,伴有反复性口疮性口炎,皮肤损伤,生殖器溃疡或血管受累,盲肠有穿孔性溃疡,无眼部受累。染色体分析揭示了两种情况下的染色体异常,包括三体性8。在先前报道的包括本病在内的所有6例伴有骨髓增生异常综合征的肠道白塞氏病患者中均显示了染色体三体性8号染色体。他们的历史表明,骨髓增生异常综合症可能是在肠道Becet病发展之前就已经开始的。这些发现表明,染色体三体性8可能在肠道白塞氏病的发病机理中起着重要作用,至少在某些人群中如此。

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