Montejo Baranda M, Perez M, De Andres J, De la Hoz C, Merino J, Aguirre C
Angiology. 1984 Sep;35(9):568-76. doi: 10.1177/000331978403500904.
We present two cases of hemorrhagic hereditary telangiectasia (HHT) or Osler-Weber-Rendu disease which started as heart failure. Both had multiple arteriovenous fistulas, one of them in a rare localization in this disease, a lower extremity. We conclude stressing the importance of thinking of HHT in the presence of obscure heart failure or arteriovenous fistulas and of looking for internal fistulas when faced by a HHT.
我们报告两例以心力衰竭起病的出血性遗传性毛细血管扩张症(HHT)或奥斯勒-韦伯-伦杜病。两例均有多发动静脉瘘,其中一例位于该病罕见部位——下肢。我们强调,在出现不明原因的心力衰竭或动静脉瘘时应考虑HHT,而面对HHT患者时应查找体内瘘。