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血友病性假肿瘤。诊断、治疗及并发症。

Hemophilic pseudotumor. Diagnosis, treatment, and complications.

作者信息

Jensen P S, Putman C E

出版信息

Am J Dis Child. 1975 Jun;129(6):717-9. doi: 10.1001/archpedi.1975.02120430053015.

Abstract

Patients with hemophilia are living longer as a result of improved therapeutic measures. Associated with this longevity is the increased occurrence of complications affecting the osseous system. One of the more serious bone complications is the hemophilic pseudotumor or hemophilic cyst. We studied its diagnosis, treatment, and complications, and report a case of an early hemophilic cyst occurring in a new location, the proximal part of the left clavicle. The increased incidence of this complication should alert the clinician to the possibility of these lesions appearing in previously unreported sites and demonstrating atypical roentgenographic features. Early recognition and treatment is essential if optimal therapeutic results are to be obtained.

摘要

由于治疗措施的改进,血友病患者的寿命延长。与这种长寿相关的是影响骨骼系统的并发症发生率增加。较严重的骨骼并发症之一是血友病性假肿瘤或血友病性囊肿。我们研究了其诊断、治疗及并发症,并报告了一例发生在新部位——左锁骨近端的早期血友病性囊肿病例。这种并发症发生率的增加应提醒临床医生,这些病变有可能出现在以前未报告的部位,并表现出非典型的X线特征。如果要获得最佳治疗效果,早期识别和治疗至关重要。

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