II型成骨不全:刮刮材料的死后组织学诊断

A. Konstantinidou, A. Souka, C. Sofocleous, H. Paraskevakou
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引用次数: 1

摘要

II型成骨不全症是一种较常见的致命性骨骼发育不良的产前发病。产前超声扫描可能提示存在严重的短肢骨骼发育不良,可以准确预测致死率,但最终的诊断、分型和亚型的具体遗传性骨骼疾病主要是基于死后的x线片。骨的组织病理学和骨的耕作可以促进各种骨骼发育不良,在成骨不全的情况下,可以诊断。我们描述了一个病例成骨不全II型诊断在14周妊娠胎儿的基础上,典型的组织病理学发现的电流材料。本报告强调了在某些骨骼发育不良的组织学诊断的效用,即使在缺乏可靠的产后x线片控制的情况下,如妊娠早期终止的刮除材料。此外,我们记录了早在妊娠第14周就存在肢体和肋骨骨折,并证实II型成骨不全症可以在妊娠早期超声扫描中出现,伴有颈部半透明增加、心室肥大和全身性水肿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Osteogenesis imperfecta type II: postmortem histological diagnosis on curettage material
Introduction Osteogenesis imperfecta type II is one of the more common lethal skeletal dysplasias with prenatal onset. The prenatal ultrasound scan may suggest the presence of severe short limb skeletal dysplasias and can accurately predict lethality, but the final diagnosis, typing and subtyping of the specific genetic skeletal disorder are mainly based on the postmortem radiography. Histopathology of the bone and car- tilage can be contributory in vari- ous skeletal dysplasias, and, in the case of osteogenesis imperfecta can be diagnostic. We describe a case of osteogenesis imperfecta type II diagnosed in a 14-week gestation foetus on the basis of the typical histopathological findings on curet- tage material. This report highlights the utility of histological diagnosis in certain skeletal dysplasias, even in the absence of reliable postmor- tem radiographic control, as is the case with curettage material in early termination of pregnancy. In addi- tion, we document the presence of limb and rib fractures as early as the 14th week of gestation, and confirm that osteogenesis imperfecta type II can present in the first-trimester ultrasound scan with increased nuchal translucency, ventriculo- megaly and generalised oedema,
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