HI多发生在梗塞灶的边缘区及皮质区，以小静脉和毛细血管出血为主。
Most HI were found at the border of the infarction focus and the cortical area, and mainly attributed to haemorrhage from small veins and capillaries.
在没有保护的情况下糖尿病患者经常并发视网膜疾病——滋养眼睛视网膜的毛细血管出血，引起视力损失。
Without protection diabetics often develop retinopathy: Tiny capillaries nourishing the retina of the eye spill blood onto the retina causing vision loss.
肺出血组肺毛细血管基质弹力纤维多处断裂，对照组阴性。
The elastic fibers of pulmonary capillary matrix broke in many place of group A but not in group B.
遗传出血性毛细血管扩张症为常染色体显性遗传病，临床少见，本文就其病理变化、临床特点进行讨论，探讨其治疗方法。附一家系25例分析。
Hereditary hemorrhagic telangiectasia is an uncommon autosomal dominant inheritance disease. 25 cases from a family were reported. The pathology, clinical presentation and treatment were discussed.
目的：探讨遗传性出血性毛细血管扩张症所引起鼻出血的治疗方法。
Objective: To study the treatment of nosebleed caused by hereditary hemorrhagic telangiectasia (HHT).
遗传性毛细血管扩张症(HHT)或Rendu - Osler - Weberdisease (ROW)是一种表现为反复出血发作的障碍。
Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease (ROW) is a disorder that presents with recurrent episodes of EPX.
遗传性毛细血管扩张症(HHT)或Rendu - Osler - Weberdisease (ROW)是一种表现为反复出血发作的障碍。
Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease (ROW) is a disorder that presents with recurrent episodes of EPX.
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