一个因子XIII缺乏的患者的自发骨破裂:一个病例报告
José M Zepeda Torres1, Essaú Brambila López1, Laura B Alegría López1
1General Surgery, High Specialty Medical Unit, Specialty Hospital, National Western Medical Center, Mexican Social Security Institute, Guadalajara, Mexico.
Radiology case reports
|July 18, 2025
概括
自发的骨破裂是一种罕见但致命的事件,特别是在XIII因子缺乏的患者中. 早期诊断和治疗对于这些高风险病例的生存至关重要.
科学领域:
- 血液学 血液学 血液学
- 外科手术病例报告
背景情况:
- 先天性XIII因子缺乏症是一种罕见的遗传性出血障碍.
- 自发骨破裂是一种危及生命的疾病,发病率很低.
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