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B型血友病的一种罕见表现:胫骨近端假肿瘤。

An unusual presentation of hemophilia B: pseudotumor of proximal tibia.

作者信息

Mittal Saurav, Arora Sumit, Khanna Shilpa, Maini Lalit, Gautam V K

机构信息

Department of Orthopedic Syrgery, Maulana Azad Medical College and Lok Nayak Hospital, New Delhi, India.

出版信息

Am J Orthop (Belle Mead NJ). 2011 Jul;40(7):E138-40.

Abstract

Hemophilia is one of the most common genetically inherited causes of bleeding disorders. The usual presentation is continuous bleeding from a wound. Very seldom, it presents as a pseudotumor of bone. When left untreated, it may induce compression and pressure necrosis of adjacent structures. Careful evaluation and a high index of suspicion are usually required to arrive at the correct diagnosis. In this article, we report the case of a 10-year-old boy with hemophilia B (Christmas disease) that presented as a pseudotumor producing a large defect in the proximal tibia.

摘要

血友病是最常见的遗传性出血性疾病病因之一。通常的表现是伤口持续出血。极少数情况下,它表现为骨假肿瘤。如果不进行治疗,可能会导致相邻结构的压迫和压迫性坏死。通常需要仔细评估和高度怀疑才能做出正确诊断。在本文中,我们报告了一例10岁患B型血友病(克里斯马斯病)的男孩病例,其表现为在胫骨近端产生大的缺损的骨假肿瘤。

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