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成骨不全合并白血病极为罕见,我院曾收治1例,现结合文献复习,将该例总结报告如下。1临床资料患儿男,7岁,因反复骨折7年、皮肤瘀点瘀斑1个月余、鼻衄1d于2005-05-20入院。患儿出生至今骨折多达20余次。1个月前,患儿全身皮肤出现散在瘀点瘀斑,1d前出现鼻衄,量多。患儿近日无发热,
Osteogenesis imperfecta associated with leukemia is extremely rare, our hospital had admitted to a case, are combined with the literature review, the case summary report is as follows. 1 Clinical data Children, male, 7 years old, due to repeated fractures for 7 years, skin petechia ecchymosis more than 1 month, epistaxis 1d in 2005-05-20 admission. Children have been fractured up to 20 times so far. A month ago, the whole body of children with scattered petechia ecchymosis, epistaxis 1d ago, the amount of more. Children have no fever recently,