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Long term treatment of recurring pathological fractures due to Mccune Albright Syndrome: Case report and literature review

机译:长期治疗Mcune Albright综合征所致的病理性骨折:病例报告和文献复习

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McCune Albright syndrome is a rare genetic disorder which is characterized by café au lait skin pigmentation, precocious puberty and polyostotic fibrous dysplasia. Treating recurring pathological fractures due to Albright syndrome is a very challenging endeavor, and more so when it is accompanied by poor bone quality and deformity. We hereby present the case of a 23-year-old male patient who is treated several times for recurrent pathological fractures of the femur at our center. We analyze the difficulties associated with treating a patient with poor bone quality over several years, discuss our treatment options, review the literature for similar cases and look at what we could have done differently. We weigh in on the difficulties in treating a severely deformed shepherd’s crook, the ways of achieving proper internal fixation and the dangers of using plating instead of an IM nail as suggested in the literature. Our main goal in reporting this case is to bring forth the unusual challenges encountered when treating patients with Albright syndrome and discussing the options of the orthopedic surgeons when treating these types of patients.
机译:McCune Albright综合征是一种罕见的遗传性疾病,其特征是咖啡厅皮肤色素沉着,性早熟和多骨性纤维性异型增生。治疗因奥尔布赖特综合症而引起的复发性病理骨折是一项非常具有挑战性的工作,当伴有骨质量差和畸形时更是如此。我们特此介绍一名23岁男性患者的案例,该患者因我们中心的股骨复发性病理性骨折接受了多次治疗。我们分析了多年来治疗骨质不良患者的困难,讨论了我们的治疗方案,回顾了类似病例的文献,并探讨了我们可以做些不同的事情。我们权衡了治疗严重变形的牧羊犬弯曲的困难,实现正确的内部固定的方法以及文献中所建议的使用电镀代替IM钉的危险。我们报告此病例的主要目的是提出治疗奥尔布赖特综合症患者时遇到的不寻常挑战,并讨论治疗此类患者时骨科医师的选择。

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