首页> 外文期刊>Respiration: International Review of Thoracic Diseases >Pulmonary capillary haemangiomatosis as a cause of pulmonary hypertension in Takayasu's aortoarteritis.
【24h】

Pulmonary capillary haemangiomatosis as a cause of pulmonary hypertension in Takayasu's aortoarteritis.

机译:肺毛细血管瘤病是高津主动脉炎引起肺动脉高压的原因。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Pulmonary hypertension is known to occur in Takayasu's aortoarteritis. It may be either due to pulmonary arterial involvement or elevated left ventricular end diastolic pressure, or both. In our case, the cause of pulmonary hypertension was a recently described rare lesion termed pulmonary capillary haemangiomatosis. This entity has a very distinct histopathologic picture. Although 19 cases have been reported in the English literature, this is the first report on pulmonary capillary haemangiomatosis producing pulmonary hypertension in Takayasu's aortoarteritis.
机译:肺动脉高压已知发生在高隆的主动脉炎中。这可能是由于肺动脉受累或左心室舒张末期压力升高,或两者都有。在我们的案例中,肺动脉高压的原因是最近描述的一种罕见的病变,称为肺毛细血管血管瘤病。该实体具有非常独特的组织病理学图像。尽管英语文献中已经报道了19例病例,但这是关于高毛津主动脉炎引起肺动脉高压的肺毛细血管血管瘤病的首次报道。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号