Hereditary hemorrhagic telangiectasia; report of a case.
Hereditary hemorrhagic telangiectasia; report of a case.
复制标题
遗传性出血性毛细血管扩张症；
DOI：
10.1016/0030-4220(57)90090-7
复制
发表时间：
1957
期刊：
影响因子：
--
通讯作者：
H. M. Syrop
中科院分区：
文献类型：
--
作者：
H. M. Syrop
1.1.结合病例报告对遗传性出血性毛细血管扩张症的发生率进行了综述。 2.2．先前关于这种疾病极其罕见及其常见口腔表现的观念似乎不再站得住脚。3.3。由于家族背景，鼻粘膜和口腔粘膜以及外部皮肤毛细血管扩张性丘疹的存在，以及这些相同区域的自发性或外伤性出血史，允许牙医直接诊断这种临床实体。4.4。之前有严重出血的记录，甚至造成一些死亡，这使得这些患者的牙科治疗并非完全没有危险。鉴于此，简要讨论治疗、注意事项和注意事项。
1.1. The incidence of hereditary hemorrhagic telangiectasia has been reviewed in conjunction with the report of a ease.2.2. Prior concepts as to the exceptional rarity of this disease with its common oral manifestations appear to be no longer tenable.3.3. By virtue of the familial background, the presence of telangiectatic papules of the nasal and oral mucosa and the external skin, together with a history of spontaneous or traumatic hemorrhages from these same areas, permits a direct diagnosis of this clinical entity by the dental practitioner.4.4. Previous records of severe hemorrhage, with some fatalities, make dental treatment for these patients not entirely without hazard. In view of this, treatment, considerations and precautions are discussed briefly.