Tang Shou-Jiang, Gordon Maggie L, Yang Victor X D, Faughnan Marie E, Cirocco Maria, Qi Bing, Yue Emily Seng, Gardiner Geoffrey, Haber Gregory B, Kandel Gabor, Kortan Paul, Vitkin Alex, Wilson Brian C, Marcon Norman E
Center for Therapeutic Endoscopy and Endoscopic Oncology, Division of Respiratory Medicine, Department of Medicine, St. Michael's Hospital, Ontario, Canada.
Gastrointest Endosc. 2003 Oct;58(4):591-8. doi: 10.1067/s0016-5107(03)01978-3.
Hereditary hemorrhagic telangiectasia is characterized by mucocutaneous telangiectases and visceral arteriovenous malformations. Knowledge is limited concerning the development hemodynamics of mucocutaneous telangiectases. Doppler optical coherence tomography can demonstrate microvascular blood flow at flow rates as low as 20 microm/second, which is up to approximately 100 times more sensitive than Doppler US. The aims of this study were to collect in vivo Doppler optical coherence tomography images of mucocutaneous telangiectases and normal surrounding mucosa and skin, and to gain experience for an in vivo GI endoscopic study. It was hypothesized that visibly normal areas may have occult telangiectases and that mucocutaneous telangiectases that have bled may have a higher rate of blood flow than mucocutaneous telangiectases with no history of bleeding.
Twelve patients with hereditary hemorrhagic telangiectasia and mucocutaneous telangiectases were studied. Two to 3 visible mucocutaneous telangiectases on the digits, lips, and tongue were imaged with Doppler optical coherence tomography, along with visually normal surrounding areas at each site. The Doppler optical coherence tomography images were obtained in 0.5 second by using 1310 nm light.
A total of 67 mucocutaneous telangiectases from the 12 patients were imaged (38 digit, 16 lip, 13 tongue). Blood flow was demonstrated within every mucocutaneous telangiectasis imaged. Doppler optical coherence tomography did not identify any abnormal vasculature within visually normal areas. Mucocutaneous telangiectases with a history of bleeding (n = 18) were situated closer to the surface, compared with mucocutaneous telangiectases with no bleeding history (n = 49), but there was no difference in the Doppler flow appearance.
Visually normal areas in patients with hereditary hemorrhagic telangiectasia did not appear to have abnormal vasculature. Mucocutaneous telangiectases with a history of bleeding were more superficial but were otherwise similar to mucocutaneous telangiectases with no bleeding history.
遗传性出血性毛细血管扩张症的特征为黏膜皮肤毛细血管扩张和内脏动静脉畸形。关于黏膜皮肤毛细血管扩张症的血流动力学发展,目前所知有限。多普勒光学相干断层扫描能够显示低至20微米/秒流速的微血管血流,其敏感性比多普勒超声高出约100倍。本研究的目的是收集黏膜皮肤毛细血管扩张症及周围正常黏膜和皮肤的体内多普勒光学相干断层扫描图像,并积累体内胃肠内镜研究的经验。研究假设为,外观正常的区域可能存在隐匿性毛细血管扩张,且有出血史的黏膜皮肤毛细血管扩张症的血流速度可能高于无出血史的黏膜皮肤毛细血管扩张症。
对12例患有遗传性出血性毛细血管扩张症及黏膜皮肤毛细血管扩张症的患者进行研究。使用多普勒光学相干断层扫描对指、唇和舌上2至3个可见的黏膜皮肤毛细血管扩张症以及每个部位外观正常的周围区域进行成像。通过使用1310纳米光在0.5秒内获取多普勒光学相干断层扫描图像。
对12例患者的总共67个黏膜皮肤毛细血管扩张症进行了成像(38个在手指,16个在嘴唇,13个在舌头)。在每个成像的黏膜皮肤毛细血管扩张症中均显示有血流。多普勒光学相干断层扫描未在外观正常的区域发现任何异常血管。与无出血史的黏膜皮肤毛细血管扩张症(n = 49)相比,有出血史的黏膜皮肤毛细血管扩张症(n = 18)位置更靠近表面,但多普勒血流表现无差异。
遗传性出血性毛细血管扩张症患者外观正常的区域似乎没有异常血管。有出血史的黏膜皮肤毛细血管扩张症位置更浅表,但在其他方面与无出血史的黏膜皮肤毛细血管扩张症相似。